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Stryker Neurovascular recalls

RecallSweep is tracking 1 recall notice naming Stryker Neurovascular in the last 180 days, issued by FDA. The most recent is dated July 1, 2026. They cover Medical Devices. Hazards cited include Fall & Tip-Over.

This page lists what the issuing agencies published. It is not a statement about Stryker Neurovascular beyond those notices — open each official notice for the authoritative detail.

Recall notices naming Stryker Neurovascular

1 recall.

FDA Class II Medical Devices ⚠ Fall & Tip-Over

Stryker Neurovascular: INZONE DETACHMENT SYSTEM, REF: M00345100950

Affected quantity: 44,937

Hazard
Embolization coil detachment system devices may experience premature battery drain causing devices to: 1) Not power on; 2) Power on with faint audible and visual indicators; 3) Be unable to detach a coil as intended, which may necessitate medical intervention if the procedure must be completed with…

Details
Embolization coil detachment system devices may experience premature battery drain causing devices to: 1) Not power on; 2) Power on with faint audible and visual indicators; 3) Be unable to detach a coil as intended, which may necessitate medical intervention if the procedure must be completed with an alternative technique. Distribution: Worldwide - US Nationwide distribution including in the states of PA, AZ, FL, CA, IL, AK, NY, MI, NJ, WI, SD, KY, AR, TX, AL, TN, MO, MA, IN, NE, WV, MT, CT, NC, VA, NV, CO, DC, DE, OH, ME, GA, WA, SC, GU, MN, OK, NH, MD, ND, UT, HI, OR, LA, MS, KS, NM, ID, IA, VT and the countries of ARGENTINA, AUSTRIA, BELGIUM, BRASIL, BULGARIA, CANADA, CANARY ISLANDS, CH…

Products affected
INZONE DETACHMENT SYSTEM, REF: M00345100950

Recall status
Ongoing

Categories

Agencies

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