Device recall
Z-2622-2017: Covidien Endo Peanut 5mm Auto Suture Blunt Dissector Item Code: 173019 The…
FDA device recall · Class II · Covidien LLC
Key facts
| Recall number (Z-number) | Z-2622-2017 |
|---|---|
| Recall event | 77300 |
| Product | Covidien Endo Peanut 5mm Auto Suture Blunt Dissector Item Code: 173019 The instrument has indications in endoscopic surgery for swabbing small amounts of fluid or for blunt dissection of soft tissue(s) and structures, or as an aid in controlling minor intraoperative bleeding |
| Product code | GCJ |
| Recalling firm | Covidien LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 13, 2019 |
| 510(k) numbers | K931962 |
| FEI number | 1219930 |
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