FDA Drug Critical Class I Ongoing

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

Reported: February 14, 2024 Initiated: November 13, 2023 #D-0299-2024

Product Description

Reason for Recall

Non-Sterility

Details

Recalling Firm: Kilitch Healthcare India Limited
Units Affected: 23,208 bottles
Distribution: Nationwide within the United States
Location: Navi Mumbai

Frequently Asked Questions

What product was recalled? ▼

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. Recalled by Kilitch Healthcare India Limited. Units affected: 23,208 bottles.

Why was this product recalled? ▼

Non-Sterility

Which agency issued this recall? ▼

This recall was issued by the FDA Drug on February 14, 2024. Severity: Critical. Recall number: D-0299-2024.