# FDA recall D-0880-2023

> **Homeocare Laboratories, Inc.** · Class II · drug recall initiated 2023-06-05.

## Product

Kanjo Homeopathic Pain Relief Cream With Arnica, NET WT 2 oz (56.70G), Manufactured  For: Acutens, Inc., Sheridan, WY NDC 80551-201-02

## Reason for recall

cGMP deviations

## Distribution

Product was distributed USA nationwide.

## Key facts

- **Recall number:** D-0880-2023
- **Recalling firm:** Homeocare Laboratories, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2023-06-05
- **Report date:** 2023-07-05
- **Termination date:** 2024-09-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Yonkers, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0880-2023

## Citation

> AI Analytics. FDA recall D-0880-2023. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/D-0880-2023. Source: US FDA. Licensed CC0.

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