Class I

Drug Recall: 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

Kilitch Healthcare India Limited · November 13, 2023

Reason for Recall

Non-Sterility

Distribution

Nationwide within the United States

States Affected

NATIONWIDE

Quantity Affected

23,208 bottles

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0299-2024

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.