ARG Laboratories recalls Pain Wizard products due to improper propylene glycol manufacturing. This affects certain 4oz tubes sold in the US. Consumers should check labels for lot number 06023C1.
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
ARG Laboratories is recalling Pain Wizard pain relief products because they used a violative grade of propylene glycol during manufacturing. This could lead to unsafe levels of the active ingredient in the product.
The product was made using a grade of propylene glycol that doesn't meet quality standards. This could result in unsafe levels of the active ingredient in the product, potentially causing health risks.
Pain Wizard users who purchased the product between 2023 and 2025 are affected. People using the product for pain relief are most at risk due to potential unsafe ingredient levels.
Check the product label for the lot number 06023C1. The product is a 4oz tube sold online at painwizard.com with a US manufacturing location.
Look for the lot number 06023C1 on the tube label.
The official recall notice states the product was made with a violative grade of propylene glycol, which could lead to unsafe levels of active ingredients. The product is not safe to use as recalled.
Check the product label for the lot number 06023C1. The product is a 4oz tube sold online at painwizard.com with a US manufacturing location.
The recall notice does not specify a remedy, so the official notice does not provide instructions for what to do with the product.
We’ve drafted a message you can send ARG Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0525-2024 — ARG Laboratories ARG Laboratories Hello, I own a ARG Laboratories that is covered by recall D-0525-2024 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.
