Synthes (USA) Products LLC Recall: Synthes Application Instrument for Sternal ZIPFIX; indi
Synthes (USA) Products LLC Recall: Synthes Application Instrument for Sternal ZIPFIX; indi is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Synthes (USA) Products LLC; Product: Synthes Application Instrument for Sternal ZIPFIX; indications for use include primary or secondary closure/re
| Recalling firm | Synthes (USA) Products LLC |
|---|---|
| Product | Synthes Application Instrument for Sternal ZIPFIX; indications for use include primary or secondary closure/repair of the sternum following sternotomy or fracture of the sternum to stabilize the sternum and promote fusion |
| Reason for recall | The end cap may loosen and detach making the instrument non-functional. No injuries reported. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Nationwide and internationally to Canada. |
| Recall initiated | 20150722 |
| Recall number | Z-2475-2015 |
| Category | device |
| State | PA |
| Country | United States |
$29/mo
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