Biomet, Inc. Recall: Biomet Integral Centralizer Hip System, Lateralized Femoral Stem (Co-
Biomet, Inc. Recall: Biomet Integral Centralizer Hip System, Lateralized Femoral Stem (Co- is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Biomet, Inc.; Product: Biomet Integral Centralizer Hip System, Lateralized Femoral Stem (Co-Cr-Mo), 9mm, 11mm, 13mm, 15mm, and 17mm; Reason for rec
| Recalling firm | Biomet, Inc. |
|---|---|
| Product | Biomet Integral Centralizer Hip System, Lateralized Femoral Stem (Co-Cr-Mo), 9mm, 11mm, 13mm, 15mm, and 17mm |
| Reason for recall | PMMA is listed as a material on the label but the product does not contain PMMA. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Worldwide distribution. US nationwide including IA, UT, MN, PA, MO, OK, IL, OH, and WA; CANADA, and NETHERLANDS |
| Recall initiated | 20151117 |
| Recall number | Z-0650-2016 |
| Category | device |
| State | IN |
| Country | United States |
$29/mo
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