Device recall
Z-0747-2021: Covidien TA Auto Suture Vascular Stapler with DST Series Technology 30mm-V 3…
FDA device recall · Class II · Covidien Llc
Key facts
| Recall number (Z-number) | Z-0747-2021 |
|---|---|
| Recall event | 86886 |
| Product | Covidien TA Auto Suture Vascular Stapler with DST Series Technology 30mm-V 3. Intended for abdominal, gynecological, pediatric and thoracic surgical procedures for resection or transection of tissue. Item Number: TA30V3S |
| Product code | GDW |
| Recalling firm | Covidien Llc |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K111825 |
| FEI number | 1282497 |
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