Biomet, Inc. Recall: PerFuse Decompression Instrument PN: 800-0541, Lot:100650. Designed t
Biomet, Inc. Recall: PerFuse Decompression Instrument PN: 800-0541, Lot:100650. Designed t is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Biomet, Inc.; Product: PerFuse Decompression Instrument PN: 800-0541, Lot:100650. Designed to access the femoral head for decompression.; Reason fo
| Recalling firm | Biomet, Inc. |
|---|---|
| Product | PerFuse Decompression Instrument PN: 800-0541, Lot:100650. Designed to access the femoral head for decompression. |
| Reason for recall | The Trocar and Plunger Assemblies are missing from the instrument, which could result in a delay in surgery greater than 30 minutes. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Distributed in the US states of CA, GA, MN, and OH, and in the Netherlands. |
| Recall initiated | 20160411 |
| Recall number | Z-1814-2016 |
| Category | device |
| State | IN |
| Country | United States |
$29/mo
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