Device recall
Z-0246-04: Product is a surgical device packaged in a box which is labeled as Sterile with…
FDA device recall · Class II · Q-Med Corporation
Key facts
| Recall number (Z-number) | Z-0246-04 |
|---|---|
| Recall event | 27613 |
| Product | Product is a surgical device packaged in a box which is labeled as Sterile with the following identification: ''PMII PROLENE Mesh Polypropylene Nonabsorbable Synthetic surgical Mesh ETHICON'' Additional infomation including comparisons between authentic Ethicon product and counterfeit are available… |
| Product code | FTL |
| Recalling firm | Q-Med Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 11, 2012 |
| FEI number | 3003157840 |
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