Gold Star Distribution recalls Claritin 20-count (UPC 655708016305) due to rodent exposure in distribution center. Consumers should check if their product was distributed by Gold Star.
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Gold Star Distribution is recalling Claritin 20-count allergy medication because their distribution center had rodent exposure. This could mean the product is contaminated with rodents, which might pose a health risk if ingested.
Rodents in the distribution center could contaminate the product with bacteria or other harmful substances. If someone ingests the contaminated medication, it might cause illness or allergic reactions.
People who bought Claritin 20-count (UPC 655708016305) from Gold Star Distribution. Those with allergies or sensitive immune systems may be at slightly higher risk if contaminated.
Check for the UPC 655708016305 on the Claritin 20-count bottle. The product was distributed by Gold Star Distribution and may have been sold between the date of the recall announcement and the expiration date.
Look for the UPC 655708016305 on the Claritin 20-count bottle to confirm if it's affected.
The recall is due to rodent exposure in the distribution center, which could mean contamination. If you have the UPC 655708016305, you should check the product details before using.
The recall record does not mention a replacement or remedy for this product.
The recall record does not specify a remedy, so you should check the product details to see if it's affected.
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-0266-2026 — Gold Star Distribution Gold Star Distribution Hello, I own a Gold Star Distribution that is covered by recall D-0266-2026 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.
