ARG Laboratories recalls Golden Tiger Pain Cream (4 oz tube) for using violative grade of propylene glycol during manufacturing. Consumers should check product details and contact the company for remedy.
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
ARG Laboratories is recalling their Golden Tiger Pain Cream because it was made with a grade of propylene glycol that doesn't meet safety standards. This could pose a health risk if the cream is used as intended.
The cream was manufactured using a grade of propylene glycol that does not meet the required specifications. This could lead to health issues if the product is used as intended, though the exact risk level is not specified in the recall.
People who own or use the Golden Tiger Pain Cream (4 oz tube) with the specific lot number and expiration date mentioned in the recall. Those with sensitive skin or allergies to ingredients in the cream may be at higher risk.
Check for the 4 oz tube labeled 'Golden Tiger Pain Cream' with the lot number 01623C1 and expiration date 01/31/2025. The product was manufactured in Albuquerque, NM.
Look for the lot number 01623C1 and expiration date 01/31/2025 on the tube.
The recall states the cream was made with a violative grade of propylene glycol, which may pose a health risk. However, the exact risk level is not specified in the recall.
The recall does not provide a specific remedy, so contact ARG Laboratories directly for further instructions.
Check for the 4 oz tube labeled 'Golden Tiger Pain Cream' with lot number 01623C1 and expiration date 01/31/2025.
We’ve drafted a message you can send ARG Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0527-2024 — ARG Laboratories ARG Laboratories Hello, I own a ARG Laboratories that is covered by recall D-0527-2024 from ARG Laboratories. 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.
