FDA Device recall Z-1182-2026
Feminine hygiene products, labeled as: KOTEX FREEDOM MAXI NO WINGS 48CT, ALWAYS THIN LINERS UNSCENTED 12 CT, ALWAYS THIN LINERS SCENTED 12C…
- FDA Device
- Class II
- ongoing
- Published 2026-02-04
On 2026-02-04 the FDA classified a Class II recall of Feminine hygiene products, labeled as: KOTEX FREEDOM MAXI NO WINGS 48CT, ALWAYS THIN LINERS UNSCENTED 12 CT, ALWAYS THIN LINERS SCENTED 12C… by Gold Star Distribution, citing potential exposure of rodents and rodent activity in the distribution center.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1182-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-12-26 |
| Published | 2026-02-04 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Gold Star Distribution |
| Distribution | US |
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, TAMPAX REG. 10CT, TAMPAX SUPER 10CT.
Reason
Potential exposure of rodents and rodent activity in the distribution center.
Identifiers
| upc | 8935107214222 |
|---|---|
| upc | 037000426882 |
| upc | 037000426899 |
| upc | 710865100653 |
| upc | 078300070320 |
| upc | 078300070245 |
| upc | 073010214095 |
| upc | 073010314092 |
| code_info | KOTEX FREEDOM MAXI NO WINGS 48CT, UPC 8935107214222; ALWAYS THIN LINERS UNSCENTED 12 CT, UPC 037000426882; ALWAYS THI…KOTEX FREEDOM MAXI NO WINGS 48CT, UPC 8935107214222; ALWAYS THIN LINERS UNSCENTED 12 CT, UPC 037000426882; ALWAYS THIN LINERS SCENTED 12CT, UPC 037000426899; ALWAYS ULT.THIN WINGS REG.12/22CT, UPC none; ALWAYS ULT.THIN OVER NIGHT WINGS 12/16CT, UPC none; JULIE MAXI NIGHT W.WINGS 36/10CT, UPC 710865100653; STAY FREE REG. 12/10CT, UPC 078300070320; STAY FREE SUPER 24/6CT, UPC 078300070245; TAMPAX REG. 10CT, UPC 073010214095; TAMPAX SUPER 10CT, UPC 073010314092. All codes purchased from this firm |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1182-2026%22
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