Device recall
Z-1099-06: Weck Hem-o-lok Endo 5 Automatic Clip Applier with Medium Polymer Ligating Clips…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-1099-06 |
|---|---|
| Recall event | 35316 |
| Product | Weck Hem-o-lok Endo 5 Automatic Clip Applier with Medium Polymer Ligating Clips; Rx, sterile, single use, disposable clip applier with medium size, non-absorbable polymer ligation clips; 15 clips per applier, 3 appliers per sales unit, 6 sales units per case; Mfg. by Weck Closure Systems, 2917 Weck… |
| Product code | FZP |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 14, 2007 |
| 510(k) numbers | K021808 |
| FEI number | 3004959265 |
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