Class I
Drug Recall: 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
Kilitch Healthcare India Limited · November 13, 2023
Reason for Recall
Non-Sterility
Distribution
Nationwide within the United States
States Affected
NATIONWIDE
Quantity Affected
137,544 bottles
Source: FDA (openFDA Drug Enforcement)
Recall number: D-0311-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.