Device recall
Z-0496-2020: WECK AutoEndo5, Automatic Hem-O-Lok Clip Applier, REF AE05ML Automatic…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0496-2020 |
|---|---|
| Recall event | 84032 |
| Product | WECK AutoEndo5, Automatic Hem-O-Lok Clip Applier, REF AE05ML Automatic Endoscopic Surgical Ligating Clip Appliers are delivery devices for Hem-o-lok ML non-absorbable polymer ligating clips |
| Product code | FZP |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K152084 |
| 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