Biomet, Inc. Recall: Compress Device Short Anchor Plug, 14 MM-For Correction of revision o
Biomet, Inc. Recall: Compress Device Short Anchor Plug, 14 MM-For Correction of revision o is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Biomet, Inc.; Product: Compress Device Short Anchor Plug, 14 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous join
| Recalling firm | Biomet, Inc. |
|---|---|
| Product | Compress Device Short Anchor Plug, 14 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178556 |
| Reason for recall | Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Ongoing |
| Distribution | Worldwide distribution - US Nationwide and the countries of ARGENTINA, AUSTRALIA, CANADA, CHILE, JAPAN, NETHERLANDS, NEW ZEALAND. |
| Recall initiated | 20231009 |
| Recall number | Z-0380-2024 |
| Category | device |
| State | IN |
| Country | United States |
$29/mo
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