Device recall
Z-2406-2024: SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM), Product Number: 1961
FDA device recall · Class II · Ethicon Sarl, a Johnson & Johnson Company
Key facts
| Recall number (Z-number) | Z-2406-2024 |
|---|---|
| Recall event | 94831 |
| Product | SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM), Product Number: 1961 |
| Product code | LMG |
| Recalling firm | Ethicon Sarl, a Johnson & Johnson Company |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3003702646 |
At a glance
- None 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