Kroger Specialty Pharmacy, Inc. recalls Orkambi 100 mg/125 mg Tablets #112 NDC 51167-0700-02 28 days supply.
Recalled May 16, 2018 · FDA recall D-0751-2018 · 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
Orkambi 100 mg/125 mg Tablets #112 NDC 51167-0700-02 28 days supply.
Manufacturer(s)
Kroger Specialty Pharmacy, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →