Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, TROJAN SPERMICIDE CO
Summary
The FDA issued a Class II for Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDO by GOLD STAR DISTRIBUTION INC. Reason: Potential exposure of rodents and rodent activity in the distribution center..
Details
Source
Device Recall
External ID
Z-1181-2026
Action Date
2026-02-04
Status
Ongoing
Category
device
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 .
Lot/Code Info: TROJAN MAGNUM CONDOMS 6/DSP BLACK, UPC 022600642039; TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, UPC 022600930501; TROJAN SPERMICIDE CONDOMS 6/DSP DARK BLUE, UPC 022600931508; TROJAN ULTRA THIN CONDOMS 6/DSP GREY, UPC 022600926207; TROJAN RIBBED CONDOMS 6/DSP GOLD/BROWN, UPC 022600940500; TROJAN NONLUBRICATED CONDOMS 6/DSP RED, UPC 22600920502; TROJAN ULTRA HER PLEASURE CONDOMS 6/DSP, UPC 022600973201; TROJAN CONDOMS MAGNUM 48 CT DISP, UPC 815556020125; *BOX TROJAN CONDOMS MAGNUM 50Ct, UPC none All codes purchased from this firm
Quantity Affected: unknown
Reason for Recall
Potential exposure of rodents and rodent activity in the distribution center.
Distribution
US Nationwide distribution in the states of Minnesota.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-12-26
Company
Minneapolis, MN
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 175 device recalls issued in the same week, part of 403 device-related FDA actions this month.
GOLD STAR DISTRIBUTION INC has 33 FDA actions in our database, including 33 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (GOLD STAR DISTRIBUTION INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does GOLD STAR DISTRIBUTION INC have FDA actions?
GOLD STAR DISTRIBUTION INC has 33 FDA actions in our database, including 33 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1181-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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