RecallRadar

FDA Drug recall D-0528-2024

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

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, Roll-… 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-0528-2024
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, Roll-On 3 fl oz (88.7ml), painwizard.com Made in the USA, PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00010 9

Reason

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

Identifiers

upc863865000109
code_infoLot 17323C3, Exp 06/30/2025

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-0528-2024%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.