fda_recall · device_recall · high

Stryker Neurovascular — Class II recall: INZONE DETACHMENT SYSTEM, REF: M00345100950

Event date
2026-07-01 00:00:00Z
Observed
2026-07-09 22:51:53Z
Source ID
Z-2552-2026
Payload hash
0773bb3d730e13385b2bc72d

Summary

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… Status: Ongoing.

Informational only. Not legal, financial, or medical advice.