CanadaThe Inzone® Detachment System (Stryker Neurovascular), model/catalogue number M00345100950, and units with lot or serial numbers of more than 10 numbers are affected. The devices were recalled because some may experience premature battery drain, which can cause them to not power on, power on with faint audible and visual indicators, or be unable to detach a coil as intended. Contact the manufacturer for additional information.
What's being recalled
Companies: Stryker Neurovascular, 47900 Bayside Parkway, Fremont, California, United States, 94538.
How to identify it
Affected products: Inzone® Detachment System; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: M00345100950
The hazard
Stryker has observed that some devices may experience premature battery drain. When this occurs, the devices may:
not power on;
power on with faint audible and visual indicators;
be unable to detach a coil as intended.
What to do
Contact the manufacturer if you require additional information.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)
United States