Device recall
Z-1179-2023: Surgipro Monofilament Polypropylene Sutures Product Description CP-535 SURGIPRO*…
FDA device recall · Class II · Covidien, LP
Key facts
| Recall number (Z-number) | Z-1179-2023 |
|---|---|
| Recall event | 91324 |
| Product | Surgipro Monofilament Polypropylene Sutures Product Description CP-535 SURGIPRO* 1 BLU 100CM GS24 X36 CP-824 SURGIPRO* 1 BLU 150CM GS26 X24 CP-825 SURGIPRO* 2 BLU 150CM GS26 X24 VP-543 SURGIPRO* 2-0 BLU 120CM V20 DA |
| Product code | GAW |
| Recalling firm | Covidien, LP |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K954808 |
| FEI number | 1219930 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 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