Recalls / Class II
Class IID-1287-2019
Product
Losartan Potassium Tablets, USP 50 mg 1000 film coated tablets Rx Only Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 SIDCO Pharmaceutical Complex, Alathur, Kanchipuram - 603 110, Tamilnadu, India. Manufactured for: Heritage Pharmaceuticals Inc., East Brunswick, NJ 08816. 1-866-901-DRUG (3784) NDC 23155-645-10
- Affected lot / code info
- Lot CLO17007A Lot CLO17008A Lot CLO17009A ; Exp 11/2019
Why it was recalled
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level at the manufacturer
Recalling firm
- Firm
- Heritage Pharmaceuticals, Inc.
- Notification channel
- Press Release
- Type
- Voluntary: Firm initiated
- Address
- 1 Tower Center Blvd Ste 1700, N/A, East Brunswick, New Jersey 08816-1145
Distribution
- Quantity
- 3012 bottles
- Distribution pattern
- Nationwide
Timeline
- Recall initiated
- 2019-05-03
- FDA classified
- 2019-05-21
- Posted by FDA
- 2019-05-29
- Terminated
- 2020-11-16
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-1287-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.