# FDA recall Z-1182-2026

> **GOLD STAR DISTRIBUTION INC** · Class II · device recall initiated 2025-12-26.

## 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 for recall

Potential exposure of rodents and rodent activity in the distribution center.

## Distribution

US Nationwide distribution in the states of Minnesota.

## Key facts

- **Recall number:** Z-1182-2026
- **Recalling firm:** GOLD STAR DISTRIBUTION INC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-12-26
- **Report date:** 2026-02-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Minneapolis, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1182-2026

## Citation

> AI Analytics. FDA recall Z-1182-2026. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-1182-2026. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*