D-0525-2024 Class II Ongoing
FDA drug recall D-0525-2024 was initiated by ARG Laboratories, Inc. on April 17, 2024 and is designated Class II. Reason for recall: Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process. The recall status is ongoing. Affected quantity: 2,864.
Recall Details
- Product Type
- Drugs
- Report Date
- June 5, 2024
- Initiation Date
- April 17, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2,864
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
Reason for Recall
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Distribution Pattern
Distributed Nationwide in the USA
Code Information
Lot , 06023C1, Exp 01/31/2025,