Device recall
Z-1182-2026: Feminine hygiene products, labeled as: KOTEX FREEDOM MAXI NO WINGS 48CT, ALWAYS…
FDA device recall · Class II · GOLD STAR DISTRIBUTION INC
Key facts
| Recall number (Z-number) | Z-1182-2026 |
|---|---|
| Recall event | 98234 |
| Product | Feminine hygiene products, labeled as: KOTEX FREEDOM MAXI NO WINGS 48CT, ALWAYS THIN LINERS UNSCENTED 12 CT, ALWAYS THIN LINERS SCENTED 12CT, ALWAYS ULT.THIN WINGS REG.12/22CT, ALWAYS ULT.THIN OVER NIGHT WINGS 12/16CT, JULIE MAXI NIGHT W.WINGS 36/10CT, STAY FREE REG. 12/10CT, STAY FREE SUPER 24/6CT… |
| Product code | HEB |
| Recalling firm | GOLD STAR DISTRIBUTION INC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K081555 |
| FEI number | 3004388746 |
At a glance
- 1–9 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