Device recall
Z-2145-2024: VICRYL Plus Antibacterial (polyglactin 910) Suture - Indicated for use in…
FDA device recall · Class II · Ethicon, Inc.
Key facts
| Recall number (Z-number) | Z-2145-2024 |
|---|---|
| Recall event | 94643 |
| Product | VICRYL Plus Antibacterial (polyglactin 910) Suture - Indicated for use in general soft tissue approximation and/or ligation, except for ophthalmic, cardiovascular and neurological tissues. PRODUCT CODE: VCP196H VCP417H VCP602H VCP603H VCP662H VCPB259H VCPB946H |
| Product code | GAM |
| Recalling firm | Ethicon, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K181652 |
| FEI number | 3017102971 |
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