Device recall
Z-0774-2023: 9 Gauge Disposable Trocars with Blunt Pushers for Use with Subcutaneous Implants…
FDA device recall · Class II · ENDO Pharmaceuticals Solutions, Inc.
Key facts
| Recall number (Z-number) | Z-0774-2023 |
|---|---|
| Recall event | 91236 |
| Product | 9 Gauge Disposable Trocars with Blunt Pushers for Use with Subcutaneous Implants Part Number: 50134-01 |
| Product code | MDM |
| Recalling firm | ENDO Pharmaceuticals Solutions, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 2243842 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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