# FDA recall D-0520-2024

> **ARG Laboratories, Inc.** · Class II · drug recall initiated 2024-04-17.

## 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

## Reason for recall

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

## Distribution

Distributed Nationwide in the USA

## Key facts

- **Recall number:** D-0520-2024
- **Recalling firm:** ARG Laboratories, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2024-04-17
- **Report date:** 2024-06-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Dallas, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0520-2024

## Citation

> AI Analytics. FDA recall D-0520-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/D-0520-2024. Source: US FDA. Licensed CC0.

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