Device recall
Z-0151-2026: BioPro Femoral Head (Ceramic heads 28-30) Product ID/Description 19023 HEAD…
FDA device recall · Class II · BioPro, Inc.
Key facts
| Recall number (Z-number) | Z-0151-2026 |
|---|---|
| Recall event | 97605 |
| Product | BioPro Femoral Head (Ceramic heads 28-30) Product ID/Description 19023 HEAD FEMORAL CERAMIC 28MM -3 19024 HEAD FEMORAL CERAMIC 28MM +0 19025 HEAD FEMORAL CERAMIC 32MM -3 19026 HEAD FEMORAL CERAMIC 32MM +0 19027 HEAD FEMORAL CERAMIC 32MM +3 |
| Product code | LZO |
| Recalling firm | BioPro, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K912641 |
| FEI number | 1832656 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database