Detachment System Recall: Stryker INZONE
Announced 2026-07-01 · FDA
The recall concerns the Stryker Neurovascular INZONE Detachment System (Ref: M00345100950) used for embolization coil detachment. Devices may experience premature battery drain, causing failure to power on, faint indicators, or inability to detach a coil, which may require medical intervention during procedures. The recall covers 44,937 units distributed worldwide, including the United States; FDA recall number is UDI-DI: 04546540697950.
| Brand | Stryker Neurovascular |
|---|---|
| Product | INZONE DETACHMENT SYSTEM, REF: M00345100950 |
| Reason | 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. |
| Severity | moderate |
| Units affected | 44937 |
| 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, CHILE, COLOMBIA, CROATIA, CZECH REPUBLIC, DENMARK, ESTONIA, FINLAND, FRANCE, GERMANY, GREECE, HONG KONG, HUNGARY, ICELAND, IRAN, IRELAND, ISRAEL, ITALIA, JAPAN, KOREA, LATVIA, LUXEMBOURG, MALAYSIA, MEXICO, NETHERLANDS, NORTHERN IRELAND, NORWAY, PHILIPPINES, POLAND, PORTUGAL, QATAR, ROMANIA, RUSSIA, SAUDI ARABIA, SINGAPORE, SLOVAKIA, SLOVENIA, SOUTH AFRICA, SOUTH PACIFIC, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, THAILAND, TURKEY, UNITED ARAB EMIRATES, UNITED KINGDOM. |
| Agency | FDA |
| Recall / campaign no. | UDI-DI: 04546540697950. Lots: WMP133638, WMP133871, WMP133872, WMP133988, WMP133989, WMP134016, WMP134132, WMP134133, WMP134234, WMP134235, WMP134255, WMP134256, WMP134380, WMP134381, WMP134432, WMP134433, WMP134518, WMP134519, WMP134609, WMP134610, WMP134794, WMP134795, WMP134939, WMP134940, WMP135187, WMP135243, WMP135302, WMP135314, WMP135354, WMP135355, WMP135387, WMP135417, WMP135473, WMP135475, WMP135491, WMP135492, WMP135623, WMP135720, WMP135727, WMP135807, WMP135865, WMP135897, WMP136084, WMP136107, WMP136190, WMP136200, WMP136611, WMP136642, WMP136736, WMP136748, WMP136852, WMP136894, WMP136985 |
WHAT YOU SHOULD DO
- If you had a procedure with this system or have concerns about battery/detachment performance, contact your healthcare provider immediately.
- Do not use any INZONE Detachment System devices until advised by your clinician or hospital.
- Facilities with potentially affected lots should review inventory and coordinate with Stryker for recall instructions and replacements as directed.
- For more information, visit the FDA recall page or contact the manufacturer and keep the recall number handy.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.