Kroger Specialty Pharmacy, Inc. recalls Pulmicort Respules 0.5 mg/2mL s, 30 days supply, NDC 00186-1989-04
Recalled May 16, 2018 · FDA recall D-0739-2018 · 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
Pulmicort Respules 0.5 mg/2mL s, 30 days supply, NDC 00186-1989-04
Manufacturer(s)
Kroger Specialty Pharmacy, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →