Cardinal Health Inc. recalls INTEGRA 325/40/3mg 90-count bottle, NDC: 52747-710-60
Recalled June 2, 2021 · FDA recall D-0588-2021 · Cardinal Health
Hazard
CGMP Deviations: Intermittent exposure to temperature excursion during storage. · FDA Class II
Units
32 bottles
Sold at
FL, GA, SC
Description
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Product
INTEGRA 325/40/3mg 90-count bottle, NDC: 52747-710-60
Manufacturer(s)
Cardinal Health Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →