ESTRADIOL 20mg PELLET — Class III drug recall D-0892-2018
Terminated recall by Qualgen, LLC, reported 2018-07-11, distributed nationwide. Labeling: Incorrect or Missing Lot and/or Exp Date.
| Recall number | D-0892-2018 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Qualgen, LLC, Edmond, OK, United States |
| Recall initiated | 2018-06-08 |
| Classified | 2018-06-29 |
| Reported by FDA | 2018-07-11 |
| Terminated | 2020-11-25 |
| Distributed | Nationwide (US) |
| Quantity | 2,940 pellets |
| Reason classes | labeling |
| NDC | 69761-0020-01 |
| Lot numbers | C211, C257, D001 |
| Expiration dates | 2018-10-03, 2018-12-14, 2019-01-02 |
Product
ESTRADIOL 20mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844 Bristol Park Blvd, Edmond OK 73013. NDC 69761-020-01
Reason for recall
Labeling: Incorrect or Missing Lot and/or Exp Date.
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-0892-2018. 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.