Epel Estradiol Pellet (Physician Preferred) – non-sterile (2014)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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
Brand
Physician Preferred Medical, LLC
Lot Codes / Batch Numbers
Lot # 06241401-070714Q, Exp 12/14
Products Sold
Lot # 06241401-070714Q, Exp 12/14
Physician Preferred Medical, LLC is recalling Epel 18 mg Estradiol Pellet, For In Office Use Only, For In Office Administration Only, Not for Resa due to Non-Sterility: The recalled lot failed sterility testing.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA drug enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Non-Sterility: The recalled lot failed sterility testing.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm, their healthcare provider, or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, KS
Page updated: Jan 13, 2026