Chemical & Lead recalls

Hazard
The paint thinner contains low-viscosity petroleum distillates, which must be in child-resistant packaging, as required by the?Poison Prevention Packaging Act. The bottles are not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young childre…

Details
This recall involves Liizousuda paint thinner bottles. The paint thinner comes in a clear bottle with a black cap and a wraparound label. The label states "Odorless Mineral Spirit" and "Artist Oil Thinning Medium" in large text.

Products affected
Liizousuda Paint Thinner

What to do
Consumers should secure the recalled paint thinner out of the sight and reach of children immediately and contact Shenzhen Gudebo Technology for information on how to obtain a replacement bottle with a child-resistant closure, into which consumers should transfer the recalled bottle's contents. Confirm on the official CPSC notice before acting.

Hazard
The recalled finger lights violate the mandatory safety standard for toys because they contain button cell batteries that can be easily accessed by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and dea…

Details
This recall involves Oitnlaughter-branded LED Finger Lights. They were sold in sets of 36 multi-colored lights. Each finger light has three internal button cell batteries that power projections of the six animal designs (tiger, elephant, rabbit, panda, butterfly and duck) when the finger light is activated.

Products affected
Oitnlaughter LED Finger Lights

What to do
Consumers should stop using the recalled toys immediately, take them away from children and contact Delightmi for a full refund. Consumers will be asked to properly dispose of the finger lights into the trash and send a photo of the disposed product to delightmi@outlook.com Note: Button cell batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedure. Confirm on the official CPSC notice before acting.

Hazard
The cup in the lunch boxes contains high lead concentration levels for drinking vessels, posing a lead poisoning hazard. Lead is toxic if ingested by adults or children and can cause adverse health issues.

Details
This recall involves the copper cup found in the Flashgitz-branded Space King No Girls Allowed Relic Lunch Boxes. The Relic Box is a retro style lunch box containing a limited-edition bundle of collectibles for fans of the web cartoon?Space King. The contents of the box are a metal figurine, a zippo lighter case, a drinking cup and a pack of condoms. The box also contains a strip of paper warning that the "Chastity Seals" is a novelty item and not intended for use. The lunch box is red with "Space King" written in red and orange lettering at the top on the front, and a picture of the Space king characters below it. Only the copper cups are included in this recall.

Products affected
Space King No Girls Allowed Relic Lunch Boxes (Cups only)

What to do
Consumers should stop using the recalled cups immediately and contact the firm for instructions on how to receive a replacement cup. Consumers who purchased the lunch boxes directly from Warren James will be sent a free replacement cup to the address previously provided in the original purchase order. Consumers should dispose of the cups in accordance with their local waste disposal requirements. The lunch box and other items that came with the box can continue to be used. Confirm on the official CPSC notice before acting.

Hazard
A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and displays two error messages back-to-back: Pump Error 53 followed immediately by Pump Error 23. Insulin delivery will stop which may lead to…

Details
A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and displays two error messages back-to-back: Pump Error 53 followed immediately by Pump Error 23. Insulin delivery will stop which may lead to delayed therapy and an increased risk of hyperglycemia or diabetic ketoacidosis (DKA). Distribution: International distribution to the countries of Spain, Great Britain, Netherlands, Italy.. Recall #Z-2698-2026, initiated 20260527. Voluntary: Firm initiated.

Products affected
MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896

Recall status
Ongoing

Hazard
Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility breach, and if breached could lead to severe infection.

Details
Distribution: Worldwide - US Nationwide distribution including in the states of NJ, WI, MI, MN, AR, UT, OH, FL, CA, TX, PA, AZ, IN, LA, NE, OK, NY, MD, WY, CO, NC, IL, GA, WA, KS, AL, MO, VA, TN, KY, MS, MA, SC, OR, WV, MT, ID, SD, CT, NV, ND, NH, DE, NM, AK, IA, DC, HI, ME, VT, RI and the countries of Great Britain, Germany, United Arab Emirates.. Recall #Z-2694-2026, initiated 20260422. Voluntary: Firm initiated.

Products affected
Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS INSTRUMENTS- DRILL EU/RLV0035-EU, INTRACEPT ACCESS INSTRUMENTS- 2VB/RLV0045, INTRACEPT ACCESS INSTRUMENTS- 2VB EU/RLV0045-EU, INTRACEPT ACCESS INSTRUMENTS- 3VB/RLV0055, INTRACEPT ACCESS INST…

Recall status
Ongoing

Hazard
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication…

Details
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss. Distribution: US Nationwide distribution in the states of AZ, CA, FL, IL, MO, NJ, OH, OK, TN, TX, WI.. Recall #Z-2609-2026, initiated 20260528. Voluntary: Firm initiated.

Products affected
Medline Convenience kits containing recalled Swan-Ganz Catheters KIT GERMANTOWN CABG DYNJ905855 KIT UNIVERSITY CABG PACK DYNJ905857 OH MED RN CDS DYNJ905936B

Recall status
Ongoing

Hazard
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication…

Details
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss. Distribution: US Nationwide distribution in the states of AZ, CA, FL, IL, MO, NJ, OH, OK, TN, TX, WI.. Recall #Z-2607-2026, initiated 20260528. Voluntary: Firm initiated.

Products affected
Medline Convenience kits containing recalled Swan-Ganz Catheters CARDIAC MAJOR DYNJ901328G HEART A DYNJ903465K OPEN HEART DYNJ909090G SILVER CROSS OPEN HEART DYNJ906102M VPH OPEN HEART DYNJ902664M DYNJ902664N

Recall status
Ongoing

Hazard
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication…

Details
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss. Distribution: US Nationwide distribution in the states of AZ, CA, FL, IL, MO, NJ, OH, OK, TN, TX, WI.. Recall #Z-2611-2026, initiated 20260528. Voluntary: Firm initiated.

Products affected
Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN HEART DYNJ909090B OPEN HEART CDS QVH CDS982523M

Recall status
Ongoing

Hazard
External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or bolus delivery. The primary failure mode is pump under-delivery due to loss of insulin to an external leak. If insulin is not delivered prop…

Details
External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or bolus delivery. The primary failure mode is pump under-delivery due to loss of insulin to an external leak. If insulin is not delivered properly, users may experience high blood glucose levels due to under-delivery of insulin. In the most severe cases, prolonged and persistent high blood glucose levels can lead to diabetic ketoacidosis (DKA), hyperglycemic hyperosmolar syndrome (HHS), or even death. Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, Switzerland, Germany, Denm…

Products affected
Omnipod 5 Pods. Includes the below Model/REF Numbers: 1. POD-OMNI-I1-6720. 2. POD-OMNI-I1-6220. 3. OMNI-I1-6729 (10-Pack), OMNI-I1-6720 (Single Pod). 4. OMNI-I1-6220. 5. OMNI-I1-6720. 6. BLE-H1-529 (10-Pack), BLE-H1-520 (Single Pod).

Recall status
Ongoing

Hazard
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication…

Details
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss. Distribution: US Nationwide distribution in the states of AZ, CA, FL, IL, MO, NJ, OH, OK, TN, TX, WI.. Recall #Z-2608-2026, initiated 20260528. Voluntary: Firm initiated.

Products affected
Medline Convenience kits containing recalled Swan-Ganz Catheters CENTRAL AND ARTERIAL LINE TOTE DYNJ8407

Recall status
Ongoing

Hazard
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been asso…

Details
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup. Distribution: Worldwide distribution - US Nationwide and the country of Canada.. Recall #Z-2550-2026, initiated 20260521. Voluntary: Firm initiated.

Products affected
Hillrom VOLARA System P.CIRCUIT KIT AC (Single Patient Use Circuit), Model/Catalog Number REF M08473; Oscillation Lung Expansion Therapy, positive pressure breathing device

Recall status
Ongoing

Hazard
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication…

Details
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss. Distribution: US Nationwide distribution in the states of AZ, CA, FL, IL, MO, NJ, OH, OK, TN, TX, WI.. Recall #Z-2612-2026, initiated 20260528. Voluntary: Firm initiated.

Products affected
Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH PACK CTX DYNJ68530A

Recall status
Ongoing

Hazard
May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible. Issue could lead to slight delay in delivery of enteral nutritional fluids or oral medication.

Details
Distribution: US distribution to the following states: AZ, CA, CO, FL, HI, IL, IN, MD, MI, MN, MO, NC, NJ, NY, OR, PA, TX, VA.. Recall #Z-2645-2026, initiated 20260605. Voluntary: Firm initiated.

Products affected
Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model/Catalog Number: ENF060182LD / 101033086 Software Version: N/A Product Description: Enteral Extension Set, Length 60 Orange-Striped Minibore Tubing, (Approx. Priming Vol. 2.00 mL), ENFit¿ Component: N/A

Recall status
Ongoing

Hazard
Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP.

Details
Distribution: U.S. Nationwide distribution including in the states and territories of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and Virgin Islands. The countries of Albania, Andorra, Argentina, Australia, Austria, Belgium, Bhutan, Canada, Canary Islands, Chile, Colombia, Costa Rica, Croatia, Cyprus, Czech Republic, Denmark, Dominican Republic, Finland, France, Georgia, Germany, Greece, Gua…

Products affected
Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 Product Codes that include the Covidien Shiley Disposable Decannulation Plug are: Product Number / UDI-DI code 4DCFN 10884522006576 4DCFS 10884522006583 4DFEN 10884522006606 6DCFN 10884522006613 6DCFS 10884522006620…

Recall status
Ongoing

Hazard
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication…

Details
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss. Distribution: US Nationwide distribution in the states of AZ, CA, FL, IL, MO, NJ, OH, OK, TN, TX, WI.. Recall #Z-2613-2026, initiated 20260528. Voluntary: Firm initiated.

Products affected
Medline Convenience kits containing recalled Swan-Ganz Catheters CABG A CDS CDS982269K CDS982269L CDS982269M CDS982269N CARDIAC MAJOR DYNJ901328D DYNJ901328F HEART A DYNJ903465F DYNJ903465G HEART TRAY-VASCULAR DYNJ907857 DYNJ907857A DYNJ907857B KIT UNIVERSITY CABG PK DYNJ905857A OPEN HEART CDS98116…

Recall status
Ongoing

Hazard
External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or bolus delivery. The primary failure mode is pump under-delivery due to loss of insulin to an external leak. If insulin is not delivered prop…

Details
External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or bolus delivery. The primary failure mode is pump under-delivery due to loss of insulin to an external leak. If insulin is not delivered properly, users may experience high blood glucose levels due to under-delivery of insulin. In the most severe cases, prolonged and persistent high blood glucose levels can lead to diabetic ketoacidosis (DKA), hyperglycemic hyperosmolar syndrome (HHS), or even death. Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, Switzerland, Germany, Denm…

Products affected
Omnipod DASH Pod. Includes the below Model/REF Numbers: 1. POD-BLE-I1-525 (5-Pack), POD-BLE-I1-520 (Single Pod). 2. POD-BLE-I1-529 (10-Pack), POD-BLE-I1-520 (Single Pod). 3. BLE-I1-529 (10-Pack), BLE-I1-520 (Single Pod). 4. BLE-C1-529 (10-Pack), BLE-C1-520 (Single Pod).

Recall status
Ongoing

Hazard
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been asso…

Details
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup. Distribution: Worldwide distribution - US Nationwide and the country of Canada.. Recall #Z-2551-2026, initiated 20260521. Voluntary: Firm initiated.

Products affected
Hillrom VOLARA System P.CIRCUIT 5KIT AC, (Single Patient Use Circuit), Model/Catalog Number REF M08474; Oscillation Lung Expansion Therapy, positive pressure breathing device

Recall status
Ongoing

Hazard
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication…

Details
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss. Distribution: US Nationwide distribution in the states of AZ, CA, FL, IL, MO, NJ, OH, OK, TN, TX, WI.. Recall #Z-2606-2026, initiated 20260528. Voluntary: Firm initiated.

Products affected
Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH PACK CTX DYNJ68530B

Recall status
Ongoing

Hazard
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication…

Details
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss. Distribution: US Nationwide distribution in the states of AZ, CA, FL, IL, MO, NJ, OH, OK, TN, TX, WI.. Recall #Z-2610-2026, initiated 20260528. Voluntary: Firm initiated.

Products affected
Medline Convenience kits containing recalled Swan-Ganz Catheters CV ANESTHESIA - ROOM SET UP DYNJ905503D DYNJ905503F DYNJ905503G

Recall status
Ongoing

Hazard
Expansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection. If particulate were to dislodg…

Details
Expansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection. If particulate were to dislodge during use and contact circulating blood or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Distribution: US Nationwide distribution in the state of TX.. Recall #Z-2615-2026, initiated 20260515. Voluntary: Firm initiated.

Products affected
Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401206RH, St. Jude Medical Response" Diagnostic Electrophysiology Catheter 4 Elec. 10mm; Item no. 401305RH, St. Jude Medical Response" Diagnostic Electrophysiology Catheter 10 Elec. 2-5-2mm.

Recall status
Ongoing

Hazard
External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or bolus delivery. The primary failure mode is pump under-delivery due to loss of insulin to an external leak. If insulin is not delivered prop…

Details
External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or bolus delivery. The primary failure mode is pump under-delivery due to loss of insulin to an external leak. If insulin is not delivered properly, users may experience high blood glucose levels due to under-delivery of insulin. In the most severe cases, prolonged and persistent high blood glucose levels can lead to diabetic ketoacidosis (DKA), hyperglycemic hyperosmolar syndrome (HHS), or even death. Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, Switzerland, Germany, Denm…

Products affected
Omnipod (Eros) Pod. Includes the below Model/REF Numbers: 1. POD-ZXP425 (10 Pack), POD- ZXP420 (Single Pod). 2. ZXR425 (10-Pack), ZXR420 (Single Pod). 3. ZXP425 (10 Pack), ZXP420 (Single Pod).

Recall status
Ongoing

Hazard
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been asso…

Details
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup. Distribution: Worldwide distribution - US Nationwide and the country of Canada.. Recall #Z-2548-2026, initiated 20260521. Voluntary: Firm initiated.

Products affected
Hillrom VOLARA System P.CIRCUIT KIT (Single Patient Use Circuit), Model/Catalog Number REF M08085; Oscillation Lung Expansion Therapy, positive pressure breathing device

Recall status
Ongoing

Hazard
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been asso…

Details
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup. Distribution: Worldwide distribution - US Nationwide and the country of Canada.. Recall #Z-2549-2026, initiated 20260521. Voluntary: Firm initiated.

Products affected
Hillrom VOLARA P.CIRCUIT 5KIT (System Single Patient Use Circuit), Model/Catalog Number REF M08270; Oscillation Lung Expansion Therapy, positive pressure breathing device

Recall status
Ongoing

Hazard
Referencing the incorrect GVWR may lead to unintentionally overloading the vehicle, increasing the risk of a crash.

Details
Forest River, Inc. (Forest River) is recalling certain 2026-2027 Wildwood and Salem travel trailers. The Federal Placard may have the incorrect Gross Vehicle Weight Rating (GVWR). As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 120, "Wheels and Rims - Other than Passenger Cars." Consequence: Referencing the incorrect GVWR may lead to unintentionally overloading the vehicle, increasing the risk of a crash.

Products affected
EQUIPMENT

What to do
Dealers will install a new corrected label, free of charge. Owner notification letters were mailed July 22, 2026. Owners may contact Forest River customer service at 1-574-534-3167. Forest River's number for this recall 04-2075. Confirm on the official NHTSA notice before acting.

Hazard
An incorrect GAWR label may lead to an overloaded vehicle, increasing the risk of a crash.

Details
Subaru of America, Inc. (Subaru) is recalling certain 2026 Crosstrek Hybrid, 2025-2026 Forester Hybrid, Forester, and 2019-2026 Ascent vehicles. These vehicles were manufactured with an incorrect Gross Axle Weight Rating (GAWR) on the certification label. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) 110, "Tire selection and rims." Consequence: An incorrect GAWR label may lead to an overloaded vehicle, increasing the risk of a crash.

Products affected
EQUIPMENT

What to do
Subaru will mail a new certification label to owners, free of charge. Owners may also choose to have a dealer install the new label, free of charge. Letters informing owners of the safety risk are expected to be mailed August 25, 2026. Additional letters will be mailed once the remedy is available.… Confirm on the official NHTSA notice before acting.

Hazard
An incorrect load carrying capacity modification label may lead to improper loading of the vehicle, increasing the risk of a crash.

Details
Southeast Toyota Distributors, LLC (SET) is recalling one 2026 Tundra truck. The current load carrying capacity modification label is incorrect. As such, this vehicle fails to comply with the requirements of Federal Motor Vehicle Safety Standard number 110, "Tire Selection and Rims." Consequence: An incorrect load carrying capacity modification label may lead to improper loading of the vehicle, increasing the risk of a crash.

Products affected
EQUIPMENT

What to do
SET will provide the owner with a new load carrying capacity modification label, free of charge. An owner notification letter is expected to be mailed September 4, 2026. The owner may contact SET's customer service at 1-866-405-4226. SET's number for this recall is SET26A. Confirm on the official NHTSA notice before acting.

Hazard
The recalled medicated wipes contain lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging of the wipes is not child-resistant, posing a risk of serious injury or death from poisoning if the contents of the wipes are ingested by you…

Details
This recall involves CVS Health Medicated Hemorrhoidal Wipes. The pain-relieving wipes were sold in boxes of 20 individually wrapped packets of flushable wipes. The CVS Health logo, a yellow heart, "Rapid Pain Relief" and "Medicated Hemorrhoidal Wipes" is printed on the front of the packet and the box.

Products affected
CVS Health Medicated Hemorrhoidal Wipes

What to do
Consumers should secure the wipes out of sight and reach of children immediately and contact CVS for a full refund. Consumers will be asked to return unopened packets of wipes with the retail box packaging to any CVS store. Confirm on the official CPSC notice before acting.

Hazard
The lithium coin batteries are not sold in child-resistant packaging and do not bear the warning labels as required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns and death.

Details
This recall involves Junpower CR2032 Batteries (20 pieces) in specific packaging (Packaging model 2023-V3). The product is packaged in a white box labeled "JUNPOWER Household Batteries," with four packs inside, each pack contains five batteries.

Products affected
Junpower CR2032 Batteries

What to do
Consumers should stop using the recalled coin batteries immediately, place them in an area that children cannot access and contact Junpower for a free replacement battery. Consumers should visit Junpower's recall page at https://www.cognitoforms.com/Junpower2032/recall and follow instructions to register for the recall. Consumers will be asked to write in permanent marker the date, their initials and the word "Recalled" on the product. Consumers should submit a photo of the marked product and properly dispose of the batteries to receive a replacement battery. Note: Button cell and coin batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedures. Confirm on the official CPSC notice before acting.

Hazard
The recalled LED finger lights violate the mandatory safety standard for toys because they contain button cell batteries that can be easily accessed by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and…

Details
This recall involves POPOOO Jungle Safari LED Finger Lights. They were sold in sets of 24 multi-colored lights with white fingertip covers. Each finger light has three internal button cell batteries that power projections of the jungle safari characters when activated. "POPOOO" and "LED FINGER LIGHTS" are printed on the product's blue packaging.

Products affected
POPOOO Jungle Safari LED Finger Lights

What to do
Consumers should stop using the recalled finger lights immediately, take them away from children and contact POPOOO for a full refund. Consumers will be asked to remove and properly dispose of the finger lights into the trash and send a photo of the disposed product to bopoorecall@outlook.com. Note: Button cell batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedures. Confirm on the official CPSC notice before acting.

Hazard
A fire increases the risk of injury.

Details
Hyundai Motor America (Hyundai) is recalling certain 2023-2024 Ioniq 5 vehicles. The high voltage battery cells may contain misaligned electrodes, which can lead to a fire while parked or driving. Consequence: A fire increases the risk of injury.

Products affected
ELECTRICAL SYSTEM

What to do
Owners are advised to park outside and away from structures and limit their charge to a maximum of 80% until the recall repair is complete. Dealers will replace the high voltage battery system assembly, free of charge. Owner notification letters are expected to be mailed August 31, 2026. Owners may… Confirm on the official NHTSA notice before acting.

Hazard
A fire increases the risk of injury.

Details
Kia America, Inc. (Kia) is recalling certain 2022-2024 EV6 and 2024 EV9 vehicles. The high voltage battery cells may contain misaligned electrodes, which can lead to a fire while parked or driving. Consequence: A fire increases the risk of injury.

Products affected
ELECTRICAL SYSTEM

What to do
Owners are advised to park outside and away from structures and limit their charge to a maximum of 80% until the recall repair is complete. Dealers will replace the high voltage battery system assembly, free of charge. Owner notification letters are expected to be mailed August 7, 2026. Owners may… Confirm on the official NHTSA notice before acting.

Hazard
GE HealthCare has become aware of a context synchronization issue in AW Server 3.2 ext. 6.5. When a user selects a patient or exam in the AW Server Web Client worklist and launches an interactive application (e.g. Volume Viewer), the application may open the previous patient's exam instead of the i…

Details
GE HealthCare has become aware of a context synchronization issue in AW Server 3.2 ext. 6.5. When a user selects a patient or exam in the AW Server Web Client worklist and launches an interactive application (e.g. Volume Viewer), the application may open the previous patient's exam instead of the intended one. When this issue occurs, there is no system warning or error notification. If the error is not recognized, a clinical user could review, interpret, or report images for the wrong patient which could lead to misdiagnosis, incorrect clinical decisions, resulting in delayed or incorrect treatment. Distribution: Worldwide distribution - United States Nationwide and the countries of Algeria…

Products affected
GE Healthcare AW Server 3.2 ext.6.5; Radiological Image Processing System

Recall status
Ongoing

Hazard
Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure to reconnect to the PIC iX central monitoring system.

Details
Distribution: US Nationwide distribution in the states of AZ, CA, CO, IN, MA, MI, MN, PA, SD, TN.. Recall #Z-2579-2026, initiated 20260605. Voluntary: Firm initiated.

Products affected
Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following system descriptions: TELE Monitor 5500, 1.4 Ghz, ECG only, ex; Telemetry Monitor 5500 1.4 GHz FAST EX.

Recall status
Ongoing

Hazard
Loose rear subframe bolts can lead to a loss of vehicle stability or rear subframe detachment, increasing the risk of a crash or injury.

Details
Honda (American Honda Motor Co.) is recalling certain 2026 Pilot and Passport vehicles. The rear subframe bolts may have been tightened improperly. Consequence: Loose rear subframe bolts can lead to a loss of vehicle stability or rear subframe detachment, increasing the risk of a crash or injury.

Products affected
STRUCTURE

What to do
Dealers will inspect and replace the rear subframe bolts as necessary, free of charge. Owner notification letters are expected to be mailed August 24, 2026. Owners may contact Honda's customer service at 1-888-234-2138. Honda's number for this recall is OOY. Vehicle Identification Numbers (VINs) in… Confirm on the official NHTSA notice before acting.

Hazard
A missing gear selection indicator may lead to unintended vehicle movement or a vehicle rollaway, increasing the risk of a crash.

Details
Nissan North America, Inc. (Nissan) is recalling certain 2026 Rogue vehicles. The instrument panel may not display the transmission gear selection indicator. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 102, "Transmission Shift Lever Sequence, Starter Interlock, and Transmission Braking Effect." Consequence: A missing gear selection indicator may lead to unintended vehicle movement or a vehicle rollaway, increasing the risk of a crash.

Products affected
POWER TRAIN

What to do
Dealers will inspect and replace the transmission control valve assembly as necessary, free of charge. Owner notification letters are expected to be mailed August 19, 2026. Owners may contact Nissan's customer service at 800-647-7261. Nissan's number for this recall is PD198. Vehicle Identification… Confirm on the official NHTSA notice before acting.

Hazard
A missing gear selection indicator may lead to unintended vehicle movement or a vehicle rollaway, increasing the risk of a crash.

Details
Chrysler (FCA US, LLC) is recalling certain 2022-2024 Jeep Grand Cherokee, 2023 Jeep Wagoneer, 2024 Jeep Grand Cherokee L, and Jeep Wagoneer L vehicles. A software error may cause the transmission gear selection indicator not to display. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 102, "Transmission shift lever sequence, starter interlock, and transmission braking effect." Consequence: A missing gear selection indicator may lead to unintended vehicle movement or a vehicle rollaway, increasing the risk of a crash.

Products affected
POWER TRAIN

What to do
Dealers will update the shifter module software, free of charge. Owner notification letters are expected to be mailed August 21, 2026. Owners may contact Chrysler customer service at 800-853-1403. Chrysler's number for this recall is 30D. Vehicle Identification Numbers (VINs) involved in this recal… Confirm on the official NHTSA notice before acting.

Hazard
Referencing incorrect weight information may lead to unintentionally overloading the vehicle, increasing the risk of a crash.

Details
Jayco, Inc. (Jayco) is recalling certain 2024 Jayco Alante and Entegra Vision recreational vehicles. The Occupant and Cargo Carrying Capacity (OCCC) label may list the incorrect weight. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) Number 120, "Wheels and Rims - other than passenger cars." Consequence: Referencing incorrect weight information may lead to unintentionally overloading the vehicle, increasing the risk of a crash.

Products affected
EQUIPMENT

What to do
Jayco will mail new correct labels, free of charge. Owner notification letters were mailed July 1, 2026. Owners may contact Jayco customer service at 1-800-283-8267. Jayco's number for this recall is 9903658. Confirm on the official NHTSA notice before acting.

Hazard
While using the pole rack at full capacity, an incorrect high vertical center of gravity during braking and cornering may lead to a loss of vehicle control, increasing the risk of a crash.

Details
Altec Industries, Inc. (Altec) is recalling certain 2023-2025 Digger Derrick vehicles. The vertical center of gravity with poles in the pole rack was not calculated properly, resulting in an incorrect pole rack capacity rating. Consequence: While using the pole rack at full capacity, an incorrect high vertical center of gravity during braking and cornering may lead to a loss of vehicle control, increasing the risk of a crash.

Products affected
EQUIPMENT

What to do
Altec will provide owners with a safety alert placard, free of charge. Owner notification letters are expected to be mailed August 21, 2026. Owners may contact Altec customer service at 1-877-462-5832. Altec's number for this recall is CSN-3335. Confirm on the official NHTSA notice before acting.

Hazard
The recalled detectors can fail to alert consumers of a fire, posing a risk of serious injury or death from smoke inhalation or burns.

Details
This recall involves Treatlife Smoke and Carbon Monoxide (CO) Detectors. The alarms are AA battery operated and have a colored light and test button. The alarms are white and circular in shape. The FCC ID "2ANDL-XR3" and the date of manufacture "2023.DEC.02" are printed on the bottom side of the alarm.

Products affected
Treatlife Smoke and Carbon Monoxide (CO) Detectors

What to do
Consumers should contact Treatlife Technology to receive a full refund. Consumers should continue using the recalled detectors until they purchase and install a replacement detector. Once a new detector is installed, consumers should write "recalled" on the recalled product, remove the batteries, dispose of the detector in their household garbage, and dispose of the batteries in accordance with local and state regulations. Confirm on the official CPSC notice before acting.

Hazard
The LED party favors violate the mandatory safety standard for consumer products because the battery compartment within the light-up products contains button cell batteries that can be easily accessed by children. When button cell or coin batteries are swallowed, the ingested batteries can cause se…

Details
This recall involves Honlyn LED party favors. The party favors include 20 LED hair fiber optic clips, 16 LED glasses, 16 foam glow sticks, 10 light-up flower crowns, 40 finger lights and 200 glow sticks. "Light Up Party Toy" is printed on the front of the product packaging. "Brand: Honlyne," "Product Name: Glow in the Dark Party Supplies" and "Mo. Number: HON-302HE" are printed on back of the product packaging. One side of the packaging bears several hazard warnings for small parts and button cell batteries.

Products affected
Honlyne LED Party Favors

What to do
Consumers should stop using the recalled party favors immediately and contact Huizhou Rongheng Network Technology for a full refund. Consumers will be asked to take a clear photo of the recalled products in the trash and email the photo to joeyrong@vip.sina.com to receive a refund. Upon verification, Huizhou Rongheng Network Technology will issue a refund. Note: Button cell batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedures. Confirm on the official CPSC notice before acting.