Epel 18 mg Estradiol Pellet — Class I drug recall D-0982-2015
Terminated recall by Physician Preferred Medical, LLC, reported 2015-05-13, distributed in AZ, KS. Non-Sterility: The recalled lot failed sterility testing.
| Recall number | D-0982-2015 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Physician Preferred Medical, LLC, Oklahoma City, OK, United States |
| Recall initiated | 2014-07-24 |
| Classified | 2015-05-04 |
| Reported by FDA | 2015-05-13 |
| Terminated | 2017-01-17 |
| Distributed | AZ, KS |
| Quantity | 122 pellets |
| Reason classes | sterility |
| Lot numbers | 06241401-070714Q, 12/14 |
Product
Epel 18 mg Estradiol Pellet, For In Office Use Only, For In Office Administration Only, Not for Resale or Dispensing to an Individual Patient, Rx Only, Preferred Physician Medical LLC, 405-551-8216
Reason for recall
Non-Sterility: The recalled lot failed sterility testing.
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-0982-2015. 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.