Inzone Detachment System
InZone Detachment System Recall Summary Stryker Neurovascular is recalling the InZone Detachment System and replacing affected units with an exchanged product. This is a Class I recall, meaning there is a serious potential health risk associated with the device. The recalled product was distributed to hospitals, pharmacies, and laboratories in New Zealand.
- Recalling firm
- Stryker New Zealand Ltd
- Product
- InZone Detachment System. [Device]. Affected: Catalogue number - 4510095 Multiple Lot numbers
- Reason
- The manufacturer has identified a problem affecting certain lots of InZone Detachment System devices. Stryker Neurovascular 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., A corrective manufacturing step has been implemented. Replacement devices are available.
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-05-12
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/266c7fa9-0926-4aa9-acff-c2760e5fd1ca