Device recall
Z-1212-2019: Covidien Endo Grasp Auto Suture Grasper 5mm REF: 173030 The Covidien Endo Grasp"…
FDA device recall · Class II · COVIDIEN LLC
Key facts
| Recall number (Z-number) | Z-1212-2019 |
|---|---|
| Recall event | 82426 |
| Product | Covidien Endo Grasp Auto Suture Grasper 5mm REF: 173030 The Covidien Endo Grasp" Auto Suture" grasper 5 mm instrument has applications in a variety of gynecologic, general, urologic, thoracic and endoscopic procedures for temporary grasping/clamping of tissue and small tubular structures. |
| Product code | HDA |
| Recalling firm | COVIDIEN LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 23, 2020 |
| 510(k) numbers | K903205 |
| FEI number | 1282497 |
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