Device recall
Z-1203-2018: Johnson & Johnson BAND-AID Brand First Aid Products SECURE-FLEX Wrap (size: 2in)
FDA device recall · Class II · Johnson & Johnson Consumer, Inc.
Key facts
| Recall number (Z-number) | Z-1203-2018 |
|---|---|
| Recall event | 79454 |
| Product | Johnson & Johnson BAND-AID Brand First Aid Products SECURE-FLEX Wrap (size: 2in) |
| Product code | FQM |
| Recalling firm | Johnson & Johnson Consumer, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 14, 2020 |
| FEI number | 2214133 |
At a glance
- None Linked 510(k)s
- 1–9 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