Recalls / Class II

Class IID-0520-2024

Product

Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Bottle with pump, NET WT 16 fluid oz / 473.17 ml, Made in USA, www.painwizard.com Pain Wizard LLC.PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00012 3

Affected lot / code info

Lot: 18723C3, Exp 06/30/2025

Why it was recalled

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

Recalling firm

Firm

ARG Laboratories, Inc.

Notification channel

Letter

Type

Voluntary: Firm initiated

Address

2639 Manana Dr, Dallas, Texas 75220-1301

Distribution

Quantity

3,440

Distribution pattern

Distributed Nationwide in the USA

Timeline

Recall initiated

2024-04-17

FDA classified

2024-05-30

Posted by FDA

2024-06-05

Status

Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-0520-2024. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.