Device recall
Z-1138-04: Staple Removal Set/Kit; a sterile Rx convenience kit containing a staple remover…
FDA device recall · Class II · Medikmark, Incorporated
Key facts
| Recall number (Z-number) | Z-1138-04 |
|---|---|
| Recall event | 29579 |
| Product | Staple Removal Set/Kit; a sterile Rx convenience kit containing a staple remover and a gauze sponge. Theses kits were marketed under the following labels, 50 kits per case: a) Medikmark inc. Staple Removal Set, reorder no. SR-2005, 3600 Bur Wood Drive, Waukegan, IL 60085; b) Maxxim Medical Staple… |
| Product code | KKX |
| Recalling firm | Medikmark, Incorporated |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 27, 2006 |
| 510(k) numbers | K920340 |
| FEI number | 1450943 |
At a glance
- 1–9 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