FDA Drug Recalls

Recalls / Class II

Class IID-0880-2023

Product

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

Affected lot / code info
Lot # 2446, exp. date Mar-24

Why it was recalled

cGMP deviations

Recalling firm

Firm
Homeocare Laboratories, Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
7 Odell Plz Ste 142-146, N/A, Yonkers, New York 10701-1407

Distribution

Quantity
921 bottles
Distribution pattern
Product was distributed USA nationwide.

Timeline

Recall initiated
2023-06-05
FDA classified
2023-06-26
Posted by FDA
2023-07-05
Terminated
2024-09-16
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0880-2023. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.