Biomet, Inc.
Frequent Recalls5
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-08-12 to 2026-08-12
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-08-12 | FDA Device | FDA Recall: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475630 Product Description: Intramedu | Biomet, Inc. | Class II | N/A |
| 2026-08-12 | FDA Device | FDA Recall: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475625 Product Description: Intramedu | Biomet, Inc. | Class II | N/A |
| 2026-08-12 | FDA Device | FDA Recall: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475620 Product Description: Intramedu | Biomet, Inc. | Class II | N/A |
| 2026-08-12 | FDA Device | FDA Recall: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475640 Product Description: Intramedu | Biomet, Inc. | Class II | N/A |
| 2026-08-12 | FDA Device | FDA Recall: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475635 Product Description: Intramedu | Biomet, Inc. | Class II | N/A |