Akorn Inc recalls Desoximetasone Ointment USP, 0.25%, a) 15 g tubes (NDC 61748-206-15 and b) 60 g tubes (NDC 61748-206-60, Marketed by Ver
Recalled November 30, 2016 · FDA recall D-0152-2017 · Akorn
Hazard
Failed Stability Specifications; out-of specification value for homogeneity / phase separation. · FDA Class II
Units
a) 62 tubes and b) 91 tubes
Sold at
Nationwide
Description
Failed Stability Specifications; out-of specification value for homogeneity / phase separation.
Product
Desoximetasone Ointment USP, 0.25%, a) 15 g tubes (NDC 61748-206-15 and b) 60 g tubes (NDC 61748-206-60, Marketed by Versapharm Inc., An Akorn Company, Lake Forest, IL, Manufactured by Hi-Tech, Pharmacal Co, Inc., Amityville, NY
Manufacturer(s)
Akorn Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →