Kilitch Healthcare India Limited: Drug Recall
Recall #D-0299-2024 · 11/13/2023
Class I: Dangerous
Recall Details
- Recall Number
- D-0299-2024
- Classification
- Class I
- Product Type
- Drug
- Recalling Firm
- Kilitch Healthcare India Limited
- Status
- Ongoing
- Date Initiated
- 11/13/2023
- Location
- Navi Mumbai, India
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 23,208 bottles
Reason for Recall
Non-Sterility
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
Distribution Pattern
Nationwide within the United States
Other Recalls by Kilitch Healthcare India Limited
- Class I: Dangerous 11/13/2023
- Class I: Dangerous 11/13/2023
- Class I: Dangerous 11/13/2023
- Class I: Dangerous 11/13/2023
- Class I: Dangerous 11/13/2023
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.