Akorn, Inc. recalls Desoximetasone Gel USP, 0.05%, packaged in 60 gram aluminum tubes, Rx only, Marketed by: VersaPharm Incorporated Mariet
Recalled August 31, 2016 · FDA recall D-1469-2016 · Akorn
Hazard
Failed impurities/degradation specifications: product was out of specification for unknown impurity at the 9 month stability time point · FDA Class III
Units
4,045 units
Sold at
Nationwide
Description
Failed impurities/degradation specifications: product was out of specification for unknown impurity at the 9 month stability time point
Product
Desoximetasone Gel USP, 0.05%, packaged in 60 gram aluminum tubes, Rx only, Marketed by: VersaPharm Incorporated Marietta, GA 30062, Manufactured by: Ei LLC Kannapolis, NC 28083, NDC 61748-205-60.
Manufacturer(s)
Akorn, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →