RecallRadar

FDA Drug recall D-0524-2024

Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Tube,…

On 2024-06-05 the FDA classified a Class II recall of Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Tube,… by Arg Laboratories, citing out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0524-2024
ClassificationClass II
Statusongoing
Initiated2024-04-17
Published2024-06-05
Last updated2026-09-13 11:52 UTC
CompanyArg Laboratories
DistributionUS

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

Reason

Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.

Identifiers

upc863865000116
code_infoLots 19823C4, EXP 07/31/2025; 01623C1, Exp 01/31/2025

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0524-2024%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.