Kroger Specialty Pharmacy, Inc. recalls Copaxone 20 mg Injection PFS (30) NDC 68546-0317-30 30 days supply.
Recalled May 16, 2018 · FDA recall D-0766-2018 · Kroger Specialty Pharmacy
Hazard
Lack of Processing Controls. · FDA Class II
Units
Unknown
Sold at
MS, LA, AR, IL, FL
Description
Lack of Processing Controls.
Product
Copaxone 20 mg Injection PFS (30) NDC 68546-0317-30 30 days supply.
Manufacturer(s)
Kroger Specialty Pharmacy, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →