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Medical Device

INZONE DETACHMENT SYSTEM, REF: M00345100950

Recall date: 2026-07-01 · Source: FDA_DEVICE
Brand / Firm
Stryker Neurovascular
Product
INZONE DETACHMENT SYSTEM, REF: M00345100950
Reason for recall
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.
Units affected
44,937
Description
INZONE DETACHMENT SYSTEM, REF: M00345100950
View official recall notice →