Bausch & Lomb recalls Lotemax (loteprednol etabonate ophthalmic gel 0.5%), Sterile, Rx Only, 5 g box, Bausch & Lomb, a division of Valeant Pha
Recalled June 19, 2019 · FDA recall D-1396-2019 · Bausch & Lomb
Hazard
Failed Stability Specifications: Out of specification for viscosity. · FDA Class III
Units
170832 bottles
Sold at
Nationwide in the U.S.
Description
Failed Stability Specifications: Out of specification for viscosity.
Product
Lotemax (loteprednol etabonate ophthalmic gel 0.5%), Sterile, Rx Only, 5 g box, Bausch & Lomb, a division of Valeant Pharmaceuticals North America LLC Bridgewater, NJ 08807 USA, NDC 24208-503-07.
Manufacturer(s)
Bausch & Lomb
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →