Estriol USP Micronized a) 100 gm NDC 62991-2159-04 — Class II drug recall D-0780-2020
Terminated recall by Letco Medical LLC, reported 2020-01-22. Subpotent
| Recall number | D-0780-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Letco Medical LLC, Decatur, AL, United States |
| Recall initiated | 2020-01-10 |
| Classified | 2020-01-15 |
| Reported by FDA | 2020-01-22 |
| Terminated | 2021-04-07 |
| Countries outside the US | AU, CA, IL, PH, TW |
| Reason classes | potency |
| NDC | 62991-2159-01, 62991-2159-02, 62991-2159-03, 62991-2159-04, 62991-2159-05, 62991-2159-06 |
| Expiration dates | 2020-06-06, 2020-08-06, 2021-04-16, 2021-08-13, 2021-09-14 |
Product
Estriol USP Micronized a) 100 gm NDC 62991-2159-04; b) 1 gm NDC 62991-2159-01; c) 1 kg NDC 62991-2159-06; d) 25 gm NDC 62991-2159-03; e) 500 gm NDC 62991-2159-05; f) 5 gm NDC 62991-2159-02, Rx Only Repackaged by: Letco Medical, LLC. Decatur, AL 35601
Reason for recall
Subpotent
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-0780-2020. 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.