Cardinal Health Inc. recalls BENICAR 40MG 30; NDC/UPC 65597010430; RX; TABLETS
Recalled June 2, 2021 · FDA recall D-0468-2021 · Cardinal Health
Hazard
CGMP Deviations: Intermittent exposure to temperature excursion during storage. · FDA Class II
Units
75 bottles
Sold at
FL, GA, SC
Description
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Product
BENICAR 40MG 30; NDC/UPC 65597010430; RX; TABLETS
Manufacturer(s)
Cardinal Health Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →