Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enri… recall
FDA recall D-0524-2024 · initiated Apr 17, 2024
ARG Laboratories, Inc. recalled Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol… in Apr 2024 — an FDA Class II recall (D-0524-2024) because Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
May cause temporary or medically reversible harm; low probability of serious harm.
Why it was recalled
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Wrong strength, or it did not keep
The product did not contain what the label promised, or stopped meeting specification before its expiry date. Under-strength medicine can mean an untreated condition.
This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.
Is your product affected? Check the lot number
A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.
Quantity recalled: 7,410
Details
- Product
- Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Tube, NET WT 8 oz (226.79g), Made in the USA, painwizard.com PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00011 6
- Recalling company
- ARG Laboratories, Inc.
- Classification
- Class II
- Status
- Ongoing
- Type
- Voluntary: Firm initiated
- Distribution
- Distributed Nationwide in the USA
- Initiated
- Apr 17, 2024
- FDA report date
- Jun 5, 2024
Frequently asked
- Was Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol… recalled?
- ARG Laboratories, Inc. recalled Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol… in Apr 2024 — an FDA Class II recall (D-0524-2024) because Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process. May cause temporary or medically reversible harm; low probability of serious harm.
- Why was Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol… recalled?
- Per the FDA enforcement record, the reason for recall D-0524-2024 was: Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
- Is a recalled Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol… dangerous to take?
- An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
- Which lots of Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol… are affected?
- Distributed: Distributed Nationwide in the USA. The recall covers these lots — Lots 19823C4, EXP 07/31/2025; 01623C1, Exp 01/31/2025. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0524-2024.