Gold Star Distribution recalls Alka Seltzer Original and Plus Cold & Flu due to rodent exposure in distribution center. Products with specific UPCs and lot numbers are affected. Consumers should check labels and contact for details.
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Gold Star Distribution is recalling Alka Seltzer Original and Plus Cold & Flu products because their distribution center had rodent exposure. This contamination risk means the products could be unsafe for consumption.
The distribution center had rodent exposure, which could lead to contamination of the products. This contamination might pose a risk of illness if consumed, though the severity is not specified in the recall.
Anyone who owns or uses the recalled Alka Seltzer products with the listed UPCs and lot numbers. People with sensitive health conditions may be at slightly higher risk due to potential contamination.
Check for the product names 'Alka Seltzer Original' or 'Plus Cold & Flu' with 58-count boxes (UPC 815556020033 or 016500514473) or 36-count boxes (UPC 016500594932).
Look for the product names and UPC codes listed in the recall notice to confirm if your product is affected.
The recall mentions rodent exposure in the distribution center, which could lead to contamination. However, the severity is not specified as causing serious injury or illness.
Check the product label for the specific UPC codes: 815556020033 (58-count box), 016500514473, or 016500594932 (36-count box).
The recall does not specify a remedy, so you should check with Gold Star Distribution for further instructions.
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-0263-2026 — Gold Star Distribution Gold Star Distribution Hello, I own a Gold Star Distribution that is covered by recall D-0263-2026 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.
