Levothroid — Class II drug recall D-432-2013
Terminated recall by Lloyd Inc. of Iowa, reported 2013-05-29, distributed nationwide. cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to de
| Recall number | D-432-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Lloyd Inc. of Iowa, Shenandoah, IA, United States |
| Recall initiated | 2013-04-01 |
| Classified | 2013-05-21 |
| Reported by FDA | 2013-05-29 |
| Terminated | 2014-05-08 |
| Distributed | Nationwide (US) |
| Quantity | 4,440 bottles |
| Reason classes | cgmp, specification failure |
| NDC | 00456-1321-01 |
| Lot numbers | 1098751, MAR-13 |
Product
Levothroid (levothyroxine sodium tablets, USP) , 50 mcg, RX only, 100 tablets per bottle, Manufactured for Forest Pharmaceuticals, Inc, St. Louis, MO by Lloyd Pharmaceutical, Shenandoah, IA, NDC 0456-1321-01
Reason for recall
cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.
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-432-2013. 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.