Gold Star Distribution recalls Carmex 12-count jars and tubes with UPCs 083078123154, 083078113155, 083078123147, 083078113148 due to rodent exposure in their facility. Products may contain rodent contamination.
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Gold Star Distribution is recalling Carmex 12-count jars and tubes with specific UPC codes because their distribution center had rodent exposure. This could mean the products contain rodent contamination, which poses a health risk.
The distribution center had rodent exposure, which could lead to contamination of the products. This means the Carmex products might contain rodent material, posing a health risk if ingested.
People who own or use Carmex 12-count jars or tubes with the listed UPC codes. Those most at risk are individuals who have used the products recently.
Check for Carmex 12-count jars with UPCs 083078123154 or 083078113155, or 12-count tubes with UPCs 083078123147 or 083078113148. All products distributed by Gold Star Distribution within their expiry dates are affected.
Look for the specific UPC codes listed: 083078123154, 083078113155 for jars, and 083078123147, 083078113148 for tubes.
The distribution center had rodent exposure, which could lead to contamination of the products.
Check for Carmex 12-count jars with UPCs 083078123154 or 083078113155, or 12-count tubes with UPCs 083078123147 or 083078113148.
The recall does not specify a remedy, so contact Gold Star Distribution for guidance.
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-0282-2026 — Gold Star Distribution Gold Star Distribution Hello, I own a Gold Star Distribution that is covered by recall D-0282-2026 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.
