Device recall
Z-1011-2019: US Endoscopy Padlock Clip defect closure system Ref: C910001 The Padlock Clip is…
FDA device recall · Class II · US Endoscopy Group Inc
Key facts
| Recall number (Z-number) | Z-1011-2019 |
|---|---|
| Recall event | 82142 |
| Product | US Endoscopy Padlock Clip defect closure system Ref: C910001 The Padlock Clip is indicated for use in flexible endoscopy and for the compression of tissue in the gastrointestinal tract, for hemostasis or for treating lesions of the wall of the gastrointestinal organs. |
| Product code | PKL |
| Recalling firm | US Endoscopy Group Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 3, 2020 |
| 510(k) numbers | K120814 |
| FEI number | 1000122656 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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