Device recall
Z-1294-2023: CoCr Femoral Head, XS, 38/-8, Taper 12/14-Intended to be used as a modular head…
FDA device recall · Class II · Zimmer, Inc.
Key facts
| Recall number (Z-number) | Z-1294-2023 |
|---|---|
| Recall event | 91842 |
| Product | CoCr Femoral Head, XS, 38/-8, Taper 12/14-Intended to be used as a modular head component for articulation in total hip arthroplasty. Item Number: 01.01012.384 |
| Product code | LPH |
| Recalling firm | Zimmer, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K993259 |
| FEI number | 1000220733 |
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