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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 70703

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
July 24, 2014
Product types
Drug
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Physician Preferred Medical, LLC

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 1

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

D-0982-2015
Recall number
D-0982-2015
Initiated
July 24, 2014
Classification
Class I
Status
Terminated
Quantity
122 Pellets

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Non-Sterility: The recalled lot failed sterility testing.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Non-Sterility: The recalled lot failed sterility testing.

Code information

Lot # 06241401-070714Q, Exp 12/14

Distribution pattern

AZ and KS