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Mckesson Medical-Surgical Inc. Corporate Office recalls MethyLPREDNISolone Acetate Injectable Suspension USP, 80 mg/mL, packaged in a) 1 mL single dose vial (NDC 0703-0051-01)

Recalled June 15, 2022 · FDA recall D-1073-2022 · Mckesson Medical-Surgical Inc. Corporate Office

Hazard
cGMP deviations: Temperature abuse · FDA Class II
Units
1088 cartons/1 vial each and 63 cartons/25 vials each
Sold at
USA nationwide.

Description

cGMP deviations: Temperature abuse

Product
MethyLPREDNISolone Acetate Injectable Suspension USP, 80 mg/mL, packaged in a) 1 mL single dose vial (NDC 0703-0051-01) b) 25-count box (NDC 0703-0051-04), Rx only, MFG: Teva Pharma USA
Manufacturer(s)
Mckesson Medical-Surgical Inc. Corporate Office

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Mckesson Medical-Surgical Inc. Corporate Office recalls MethyLPREDNISolone Acetate Injectable Suspension USP, 80 mg/mL, packaged in a) 1 mL single dose vial (NDC 0703-0051-01) | RecallWatchUSA