Homeocare Laboratories, Inc.: Drug Recall
Recall #D-0880-2023 · 06/05/2023
Class II: Risk
Recall Details
- Recall Number
- D-0880-2023
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Homeocare Laboratories, Inc.
- Status
- Terminated
- Date Initiated
- 06/05/2023
- Location
- Yonkers, NY, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 921 bottles
Reason for Recall
cGMP deviations
Product Description
Kanjo Homeopathic Pain Relief Cream With Arnica, NET WT 2 oz (56.70G), Manufactured For: Acutens, Inc., Sheridan, WY NDC 80551-201-02
Distribution Pattern
Product was distributed USA nationwide.
Other Recalls by Homeocare Laboratories, Inc.
- Class II: Risk 06/05/2024
- Class I: Dangerous 06/05/2024
- Class II: Risk 06/05/2023
- Class II: Risk 06/05/2023
- Class II: Risk 06/05/2023
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.