Akorn, Inc. recalls Atropine Sulfate Ophthalmic 1% Solution, USP, 5mL per bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake Fores
Recalled March 14, 2018 · FDA recall D-0577-2018 · Akorn
Hazard
Failed Stability Specification: OOS low viscosity results discovered during retain testing. · FDA Class III
Units
31,812 bottles
Sold at
Nationwide in the USA
Description
Failed Stability Specification: OOS low viscosity results discovered during retain testing.
Product
Atropine Sulfate Ophthalmic 1% Solution, USP, 5mL per bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-215-05
Manufacturer(s)
Akorn, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →