Drug recall D-0463-2021
Product
Meloxicam Tablets, USP 7.5 mg 100 Tablets Rx Only NDC 69097-158-07 Manufactured for: Cipla USA, Inc. 9100 S. Dadeland Blvd., Suite 1500 Miami, FL 33156
Reason for recall
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots and codes
KA03034
Recall details
- Recalling firm
- Cardinal Health Inc., Dublin, OH
- Quantity
- 576 bottles
- Distribution
- FL, GA, SC
- Type
- Voluntary: Firm initiated
- Recall initiated
- March 15, 2021
- Terminated
- June 17, 2024
Related products
- Meloxicam – drug information
- NDC 69097-158 Meloxicam · Meloxicam 7.5 mg/1 · Cipla USA Inc.
- NDC 69097-159 Meloxicam · Meloxicam 15 mg/1 · Cipla USA Inc.