Gold Star Distribution recalls specific TYLENOL products due to rodent exposure in their distribution center. Consumers should check product labels for affected lots and contact the company for details.
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Gold Star Distribution is recalling several TYLENOL products because their distribution center had rodent exposure. This could lead to contamination of the products, though the risk is not described as causing serious injury.
The distribution center had rodent activity, which could have contaminated the products with bacteria or other harmful substances. This poses a risk of infection or illness if the contaminated products are taken internally.
People who purchased any of the listed TYLENOL products from Gold Star Distribution. Those with allergies to the ingredients or who use the products frequently may be at slightly higher risk.
Check the product label for the specific TYLENOL products listed: 500 MG, 2's display, 50ct; Cold & Flu, 25ct/2s; Cold & Flu Severe, 2pk, 50ct; PM, 50ct; or Sinus Severe, 2pk, 50ct. All lots distributed by Gold Star Distribution are affected.
Look for the specific TYLENOL products listed in the recall notice on the label.
Yes, all lots distributed by Gold Star Distribution are affected.
The recall notice does not specify a remedy, so contact Gold Star Distribution for further instructions.
The recall states rodent exposure, but does not mention serious injury risks. The danger level is low risk.
We’ve drafted a message you can send Gold Star Distribution to request your refund or repair — edit it as you like.
Subject: Recall D-0277-2026 — Gold Star Distribution Gold Star Distribution Hello, I own a Gold Star Distribution that is covered by recall D-0277-2026 from Gold Star Distribution. 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.
