Device recall
Z-1530-2022: SKYN ORIGINAL NON LATEX CONDOM 12CT, SKU 903409 LS SKYN NON LATEX LUBRICATED…
FDA device recall · Class II · Family Dollar Stores, Llc.
Key facts
| Recall number (Z-number) | Z-1530-2022 |
|---|---|
| Recall event | 90650 |
| Product | SKYN ORIGINAL NON LATEX CONDOM 12CT, SKU 903409 LS SKYN NON LATEX LUBRICATED CONDOM 3CT, SKU 900794 SKYN ELITE NON LATEX CONDOM 12CT, SKU 903415 |
| Product code | MOL |
| Recalling firm | Family Dollar Stores, Llc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K160399 |
| FEI number | 1036966 |
At a glance
- 1–9 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