Device recall
Z-2545-2019: LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical…
FDA device recall · Class III · CooperSurgical, Inc.
Key facts
| Recall number (Z-number) | Z-2545-2019 |
|---|---|
| Recall event | 83704 |
| Product | LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures. |
| Product code | GEI |
| Recalling firm | CooperSurgical, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 14, 2020 |
| 510(k) numbers | K120476 |
| FEI number | 1216677 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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