Homeocare Laboratories, Inc.: Drug Recall

Recall #D-0881-2023 · 06/05/2023

Class II: Risk

Recall Details

Recall Number
D-0881-2023
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
2,376 bottles

Reason for Recall

cGMP deviations

Product Description

Arnica 7 Cream, net wt 2 oz (56.7g), Manufactured for: Brazmedics, LLC, New York, NY 10021 UPC 8 60208 00181 6

Distribution Pattern

Product was distributed USA nationwide.

Other Recalls by Homeocare Laboratories, Inc.

View all recalls by Homeocare Laboratories, Inc. →

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.