Recall Z-1182-2026— GOLD STAR DISTRIBUTION INC

Name: FDA recall Z-1182-2026
Creator: U.S. Food and Drug Administration
Published: 2025-12-26

Class II · Ongoing

Class II FDA medical device recall by GOLD STAR DISTRIBUTION INC, initiated 2025-12-26. It names one FDA 510(k) clearance: K081555. 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..

Recalling firm: GOLD STAR DISTRIBUTION INC
Classification: Class II
Status: Ongoing
Initiated: 2025-12-26
Firm location: Minneapolis, MN, United States

510(k) clearances named in this recall

1 on FDA's record

K081555 — TAMPAX PEARL PLASTIC APPLICATOR TAMPONS, SCENTED AND UNSCENTEDProcter & Gamble Co.·cleared 2008-06-27

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.