Recall Z-1181-2026— GOLD STAR DISTRIBUTION INC

Name: FDA recall Z-1181-2026
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: K874383. Product: Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, TROJAN SPERMICIDE CONDOMS 6/DSP DARK BLUE, TROJAN ULTRA THIN CONDOMS 6/DSP GREY, TROJAN RIBBED CONDOMS 6/DSP GOLD/BROWN, TROJAN NONLUBRICATED CONDOMS 6/DSP RED, TROJAN ULTRA HER PLEASURE CONDOMS 6/DSP, TROJAN CONDOMS MAGNUM 48 CT DISP, *BOX TROJAN CONDOMS MAGNUM 50CT .. 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

K874383 — MENTOR PLUS (CONDOM)Arcon Corp.·cleared 1988-03-07

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

Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, TROJAN SPERMICIDE CONDOMS 6/DSP DARK BLUE, TROJAN ULTRA THIN CONDOMS 6/DSP GREY, TROJAN RIBBED CONDOMS 6/DSP GOLD/BROWN, TROJAN NONLUBRICATED CONDOMS 6/DSP RED, TROJAN ULTRA HER PLEASURE CONDOMS 6/DSP, TROJAN CONDOMS MAGNUM 48 CT DISP, *BOX TROJAN CONDOMS MAGNUM 50CT .

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.