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.