FDA Drug recall D-0982-2015
Epel 18 mg Estradiol Pellet, For In Office Use Only, For In Office Administration Only, Not for Resale or Dispensing to an Individual Patie…
- FDA Drug
- Class I
- terminated
- Published 2015-05-13
On 2015-05-13 the FDA classified a Class I recall of Epel 18 mg Estradiol Pellet, For In Office Use Only, For In Office Administration Only, Not for Resale or Dispensing to an Individual Patie… by Physician Preferred Medical, citing non-Sterility: The recalled lot failed sterility testing.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0982-2015 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2014-07-24 |
| Published | 2015-05-13 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Physician Preferred Medical |
| Distribution | AZ, KS |
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
Non-Sterility: The recalled lot failed sterility testing.
Identifiers
| code_info | Lot # 06241401-070714Q, Exp 12/14 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0982-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.