Device recall
Z-1098-06: Weck Hem-o-lok XL Polymer Ligating Clips; Rx, sterile, extra large size…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-1098-06 |
|---|---|
| Recall event | 35316 |
| Product | Weck Hem-o-lok XL Polymer Ligating Clips; Rx, sterile, extra large size, non-absorbable polymer ligation clips; 6 clips per cartridge, 14 cartridges per sales unit, 12 sales units per case; Mfg. by Weck Closure Systems, Research Triangle Park, NC 27709; REF 544250 |
| Product code | FZP |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 14, 2007 |
| 510(k) numbers | K030311 |
| 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