Kilitch Healthcare India Limited recalls Leader brand Dry Eye Relief (Polyethylene glycol 400 0.4% and Propylene glycol 0.3%) packaged in 0.33 FL OZ (10 mL) bott
Recalled February 14, 2024 · FDA recall D-0295-2024 · Kilitch Healthcare India
Hazard
Non-Sterility · FDA Class I
Units
12,960 bottles
Sold at
Nationwide within the United States
Description
Non-Sterility
Product
Leader brand Dry Eye Relief (Polyethylene glycol 400 0.4% and Propylene glycol 0.3%) packaged in 0.33 FL OZ (10 mL) bottles, Distributed by Cardinal Health Dublin, Ohio 43017, NDC 70000-0088-1
Manufacturer(s)
Kilitch Healthcare India Limited
Made in
India
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →