Device recall
Z-1541-2022: NEW SKIN LIQUID BANDAGE CLEAR.3FL OZ, SKU 999417
FDA device recall · Class II · Family Dollar Stores, Llc.
Key facts
| Recall number (Z-number) | Z-1541-2022 |
|---|---|
| Recall event | 90650 |
| Product | NEW SKIN LIQUID BANDAGE CLEAR .3FL OZ, SKU 999417 |
| Product code | KMF |
| Recalling firm | Family Dollar Stores, Llc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1036966 |
At a glance
- None Linked 510(k)s
- 10–99 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