Device recall
Z-0152-2026: BioPro Endo Head (Ceramic) Product ID/Description 13006 ENDO MODULAR CERAMIC SH…
FDA device recall · Class II · BioPro, Inc.
Key facts
| Recall number (Z-number) | Z-0152-2026 |
|---|---|
| Recall event | 97605 |
| Product | BioPro Endo Head (Ceramic) Product ID/Description 13006 ENDO MODULAR CERAMIC SH 38 13012 ENDO MODULAR CERAMIC SH 51 13013 ENDO MODULAR CERAMIC MD 38 13019 ENDO MODULAR CERAMIC MD 51 13007 ENDO MODULAR CERAMIC SH 41 13008 ENDO MODULAR CERAMIC SH 43 13009 ENDO MODULAR CERAMIC SH 45 13010 ENDO MODULAR… |
| Product code | LZY |
| Recalling firm | BioPro, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K954768 |
| FEI number | 1832656 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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