D-0880-2023 Class II Terminated
FDA drug recall D-0880-2023 was initiated by Homeocare Laboratories, Inc. on June 5, 2023 and is designated Class II. Reason for recall: cGMP deviations The recall status is terminated (terminated September 16, 2024). Affected quantity: 921 bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- July 5, 2023
- Initiation Date
- June 5, 2023
- Termination Date
- September 16, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 921 bottles
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
Reason for Recall
cGMP deviations
Distribution Pattern
Product was distributed USA nationwide.
Code Information
Lot # 2446, exp. date Mar-24