503recalls · last 30 days
40CPSC · last 30 days
394FDA · last 30 days
66NHTSA · last 30 days
3FSIS · last 30 days
3,579in 180-day window

Argon Medical Devices, Inc recalls

RecallSweep is tracking 6 recall notices naming Argon Medical Devices, Inc in the last 180 days, issued by FDA. The most recent is dated July 22, 2026. They cover Medical Devices. 6 carry a Class I or Do Not Drive designation.

This page lists what the issuing agencies published. It is not a statement about Argon Medical Devices, Inc beyond those notices — open each official notice for the authoritative detail.

Recall notices naming Argon Medical Devices, Inc

6 recalls.

FDA Class I Medical Devices

Argon Medical Devices, Inc: General Biospy Tray, REF: GUTS1000

Affected quantity: 1800

Hazard
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

Details
Distribution: Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago.. Recall #Z-2706-2026, initiated 20260601. Voluntary: Firm initiated.

Products affected
General Biospy Tray, REF: GUTS1000

Recall status
Ongoing

FDA Class I Medical Devices

Argon Medical Devices, Inc: Arterial Line Kit 20ga x 6, REF: 400115A

Affected quantity: 440

Hazard
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

Details
Distribution: Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago.. Recall #Z-2708-2026, initiated 20260601. Voluntary: Firm initiated.

Products affected
Arterial Line Kit 20ga x 6, REF: 400115A

Recall status
Ongoing

FDA Class I Medical Devices

Argon Medical Devices, Inc: Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F, REF: 008416A, 008566A

Affected quantity: 950

Hazard
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

Details
Distribution: Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago.. Recall #Z-2704-2026, initiated 20260601. Voluntary: Firm initiated.

Products affected
Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F, REF: 008416A, 008566A

Recall status
Ongoing

FDA Class I Medical Devices

Argon Medical Devices, Inc: One-Piece Introducer Tray, REF: 497455, 497434 cardiovascular

Affected quantity: 200

Hazard
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

Details
Distribution: Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago.. Recall #Z-2705-2026, initiated 20260601. Voluntary: Firm initiated.

Products affected
One-Piece Introducer Tray, REF: 497455, 497434 cardiovascular

Recall status
Ongoing

FDA Class I Medical Devices

Argon Medical Devices, Inc: T-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATL

Affected quantity: 850

Hazard
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

Details
Distribution: Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago.. Recall #Z-2707-2026, initiated 20260601. Voluntary: Firm initiated.

Products affected
T-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATL

Recall status
Ongoing

FDA Class I Medical Devices

Argon Medical Devices, Inc: Bone Marrow Tray, REF: CB0033TL; CB0355TLA

Affected quantity: 680

Hazard
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

Details
Distribution: Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago.. Recall #Z-2709-2026, initiated 20260601. Voluntary: Firm initiated.

Products affected
Bone Marrow Tray, REF: CB0033TL; CB0355TLA

Recall status
Ongoing

Categories

Agencies

Other brands recalled in the same categories

Browse