ARG Laboratories, Inc.: Drug Recall
Recall #D-0525-2024 · 04/17/2024
Class II: Risk
Recall Details
- Recall Number
- D-0525-2024
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- ARG Laboratories, Inc.
- Status
- Ongoing
- Date Initiated
- 04/17/2024
- Location
- Dallas, TX, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2,864
Reason for Recall
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Product Description
Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Tube, NET WT 4oz (113.39g), painwizard.com Made in the USA, PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00019 2
Distribution Pattern
Distributed Nationwide in the USA
Other Recalls by ARG Laboratories, Inc.
- Class II: Risk 04/17/2024
- Class II: Risk 04/17/2024
- Class II: Risk 04/17/2024
- Class II: Risk 04/17/2024
- Class II: Risk 04/17/2024
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.