Data Foundry

Drug recalls 2023

TIROSINT — Class II drug recall D-0341-2023

Terminated recall by IBSA PHARMA INC, reported 2023-03-01, distributed nationwide. Subpotent Drug

Recall numberD-0341-2023
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmIBSA PHARMA INC, Parsippany, NJ, United States
Recall initiated2023-01-30
Classified2023-04-04
Reported by FDA2023-03-01
Terminated2023-10-31
DistributedNationwide (US)
Reason classespotency
NDC71858-0105, 71858-0105-01, 71858-0105-02, 71858-0105-04, 71858-0105-05, 71858-0105-06, 71858-0110, 71858-0110-01, 71858-0110-02, 71858-0110-04, 71858-0110-05, 71858-0110-06, 71858-0112, 71858-0112-01, 71858-0112-02, 71858-0112-04, 71858-0112-05, 71858-0112-06, 71858-0113, 71858-0113-01, 71858-0113-02, 71858-0113-04, 71858-0113-05, 71858-0113-06, 71858-0115 and 65 more
Lot numbers220411, 220854
Expiration dates2023-10, 2024-02

Product

TIROSINT - SOL (levothyroxine sodium) Oral Solution, 88 microgram/mL; 6 pouches x 5 ampules, Rx Only; Manufactured for IBSA Pharma Inc. by: IBSA Institut Biochimique SA, 6912 Pazzallo, Switzerland; Distributed by: IBSA Pharma Inc., Parsippany, NJ 07054; NDC 71858-0125-5

Reason for recall

Subpotent Drug

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-0341-2023. 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.