TROJAN condoms with specific UPC codes were recalled due to potential rodent exposure in distribution centers. Consumers should check product labels for affected models and contact the manufacturer for details.
Potential exposure of rodents and rodent activity in the distribution center.
TROJAN condoms with certain labels and UPC codes were recalled because rodents may have been present during distribution. This could lead to contamination with rodent pathogens. Consumers should check their product labels to see if they are affected.
Rodents may have been present in the distribution center where the condoms were stored, potentially contaminating them with rodent pathogens. This could lead to exposure to harmful bacteria or viruses if the condoms are used.
Anyone who owns or uses TROJAN condoms with the specific labels and UPC codes listed in the recall. People most at risk are those who have used the affected condoms recently.
Check the condom label for the specific product names and UPC codes listed in the recall. Affected items include TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, and other models with the listed UPC numbers.
Look for the specific product names and UPC codes listed in the recall to determine if your condoms are affected.
The recall was issued because rodents may have been present in the distribution center, potentially contaminating the condoms with rodent pathogens.
Check the label for the specific product names and UPC codes listed in the recall, such as TROJAN MAGNUM CONDOMS 6/DSP BLACK or UPC 022600642039.
The recall does not specify a remedy, so you should check the product labels and contact the manufacturer for further instructions.
We’ve drafted a message you can send TROJAN to request your refund or repair — edit it as you like.
Subject: Recall Z-1181-2026 — TROJAN TROJAN Hello, I own a TROJAN that is covered by recall Z-1181-2026 from TROJAN. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
