RecallRadar

FDA Drug recall D-0484-2021

EZETIMIBE AND SIMVASTATIN TABLETS 10-10MG 30

On 2021-06-02 the FDA classified a Class II recall of EZETIMIBE AND SIMVASTATIN TABLETS 10-10MG 30 by Cardinal Health, citing CGMP Deviations: Intermittent exposure to temperature excursion during storage.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0484-2021
ClassificationClass II
Statusterminated
Initiated2021-03-15
Published2021-06-02
Last updated2026-09-13 11:52 UTC
CompanyCardinal Health
DistributionFL, GA, SC

Product

EZETIMIBE AND SIMVASTATIN TABLETS 10-10MG 30; NDC/UPC 68462-321-30; RX; TABLETS

Reason

CGMP Deviations: Intermittent exposure to temperature excursion during storage.

Identifiers

ndc68462-321-90
ndc68462-321-10
ndc68462-321-30
ndc68462-322-30
ndc68462-322-90
ndc68462-322-10
ndc68462-323-30
ndc68462-323-90
ndc68462-323-05
ndc68462-324-30
ndc68462-324-90
ndc68462-324-05
code_info17201603

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0484-2021%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.