Bayer 25-count tablets distributed by Gold Star Distribution are recalled due to rodent exposure risks in their facilities. Consumers should check their lot numbers and contact the manufacturer for details.
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Bayer 25-count tablets distributed by Gold Star Distribution are being recalled because of unsanitary conditions in their distribution center that may have exposed the product to rodents. This could pose a risk of contamination from rodent activity.
The distribution center had unsanitary conditions including rodent exposure or activity, which could lead to contamination of the tablets. This contamination might introduce harmful substances from rodents into the product.
Owners of Bayer 25-count tablets distributed by Gold Star Distribution are affected. People with compromised immune systems may be at higher risk due to potential contamination.
Check the product label for the Bayer 25-count tablets distributed by Gold Star Distribution. The recall includes all lots within the expiration date that were distributed by this company.
Look for the Bayer 25-count tablets distributed by Gold Star Distribution on the label.
The recall does not specify if the tablets are safe to use; they are being recalled due to potential rodent contamination risks.
Check the product label for Bayer 25-count tablets distributed by Gold Star Distribution; all lots within the expiration date are included in this recall.
The recall does not specify a remedy, so contact the manufacturer for further instructions.
We’ve drafted a message you can send Bayer to request your refund or repair — edit it as you like.
Subject: Recall D-0265-2026 — Bayer Bayer Hello, I own a Bayer that is covered by recall D-0265-2026 from Bayer. 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.
