Device recall
Z-0886-2016: Auto Endo5 Hem-o-lok Automatic Clip Applier, Medium Large Polymer Clips, Rx…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0886-2016 |
|---|---|
| Recall event | 73181 |
| Product | Auto Endo5 Hem-o-lok Automatic Clip Applier, Medium Large Polymer Clips, Rx Only, Sterile, REF 543965 Product Usage: The Weck Auto Endo5 hem-o-lok ML automatic endoscopic ligating clip appliers are indicated for use as delivery devices for Hem-o-lok ML non-absorbable polymer ligating clips. These… |
| Product code | FZP |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 11, 2017 |
| 510(k) numbers | K142777 |
| 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