Device recall
Z-0992-2018: DELTA CER FEM HD 32/0MM T1 Product Usage: For use in hip arthroplasty
FDA device recall · Class II · Zimmer Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-0992-2018 |
|---|---|
| Recall event | 79242 |
| Product | DELTA CER FEM HD 32/0MM T1 Product Usage: For use in hip arthroplasty |
| Product code | LZO |
| Recalling firm | Zimmer Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 13, 2018 |
| 510(k) numbers | K131684 |
| FEI number | 1825034 |
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