Device recall
Z-1136-04: Staple Removal Tray/Set/Kit; a sterile Rx convenience kit containing a staple…
FDA device recall · Class II · Medikmark, Incorporated
Key facts
| Recall number (Z-number) | Z-1136-04 |
|---|---|
| Recall event | 29579 |
| Product | Staple Removal Tray/Set/Kit; a sterile Rx convenience kit containing a staple remover instrument, an alcohol prep pad, a PVP prep pad and a gauze sponge. Theses kits were marketed under the following labels, 50 kits per case: a) Medikmark inc. Staple Removal Tray, reorder no. RS-2000, 3600 Bur Wood… |
| 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