Device recall
Z-0547-04: Hem-o-LokSMX Legating Clip, REF 544220, Lot 988384, Non-absorbable Polymer…
FDA device recall · Class II · Weck
Key facts
| Recall number (Z-number) | Z-0547-04 |
|---|---|
| Recall event | 28248 |
| Product | Hem-o-LokSMX Legating Clip, REF 544220, Lot 988384, Non-absorbable Polymer Ligation Clips, Sterile EO, Weck Closure Systems, Research Triangle Park, NC 27709, Sterile, Single use, Disposable. |
| Product code | FZP |
| Recalling firm | Weck |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 11, 2004 |
| 510(k) numbers | K982941 |
| FEI number | 3005747797 |
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