Kilitch Healthcare India Limited: Drug Recall
Recall #D-0311-2024 · 11/13/2023
Class I: Dangerous
Recall Details
- Recall Number
- D-0311-2024
- 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
- 137,544 bottles
Reason for Recall
Non-Sterility
Product Description
Up&Up brand dry eye relief (Carboxymethylcellulose 0.5%) packaged in 0.5 FL OZ (15 mL) each bottles (Twin Pack), Distributed by: Target Corporation Minneapolis, MN 55403, NDC 76168-800-30
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.