Data Foundry

Drug recalls 2021

TIROSINT — Class II drug recall D-0495-2021

Terminated recall by Cardinal Health Inc., reported 2021-06-02, distributed in FL, GA, SC. CGMP Deviations: Intermittent exposure to temperature excursion during storage.

Recall numberD-0495-2021
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmCardinal Health Inc., Dublin, OH, United States
Recall initiated2021-03-15
Classified2021-05-24
Reported by FDA2021-06-02
Terminated2024-06-17
DistributedFL, GA, SC
Quantity25 boxes
Reason classescgmp, temperature control
NDC71858-0005, 71858-0005-01, 71858-0005-02, 71858-0005-04, 71858-0010, 71858-0010-01, 71858-0010-02, 71858-0010-04, 71858-0012, 71858-0012-01, 71858-0012-02, 71858-0012-04, 71858-0013, 71858-0013-01, 71858-0013-02, 71858-0013-04, 71858-0015, 71858-0015-01, 71858-0015-02, 71858-0015-04, 71858-0017, 71858-0017-01, 71858-0017-02, 71858-0017-04, 71858-0020 and 35 more

Product

TIROSINT(levothyroxine sodium) capsules 175MCG 3 blisters X10 capsules; NDC/UPC 71858-0055-4; RX; CAPSULES

Reason for recall

CGMP Deviations: Intermittent exposure to temperature excursion during storage.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0495-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.