D-0299-2024 Class I Ongoing
FDA drug recall D-0299-2024 was initiated by Kilitch Healthcare India Limited on November 13, 2023 and is designated Class I. Reason for recall: Non-Sterility The recall status is ongoing. Affected quantity: 23,208 bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- February 14, 2024
- Initiation Date
- November 13, 2023
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 23,208 bottles
Product Description
Leader brand Dry Eye Relief (Carboxymethylcellulose Sodium 1%), packaged in 0.5 FL OZ (15 mL) bottles, Cardinal Health Dublin, Ohio 43017, NDC 70000-0089-1
Reason for Recall
Non-Sterility
Distribution Pattern
Nationwide within the United States
Code Information
All lots