Recalls / Class II
Class IID-0881-2023
Product
Arnica 7 Cream, net wt 2 oz (56.7g), Manufactured for: Brazmedics, LLC, New York, NY 10021 UPC 8 60208 00181 6
- Affected lot / code info
- Lot # 2446, exp. 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
- 2,376 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-0881-2023. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.