Kroger Specialty Pharmacy, Inc. recalls Bethkis 300 mg/4 mL Ampule #56 NDC 10122-0820-56 56 days supply
Recalled May 16, 2018 · FDA recall D-0752-2018 · 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
Bethkis 300 mg/4 mL Ampule #56 NDC 10122-0820-56 56 days supply
Manufacturer(s)
Kroger Specialty Pharmacy, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →