Drug recall

Estradiol 1.25 mg, Progesterone 25 mg/mL injectable, 20 mL sterile vials, The Apothecary Shoppe, 6136 E. 51st…

FDA recall event 66241 · Class II · Apothecary Shoppe

Key facts

Event ID 66241
Recall numbers D-66241-001, D-66241-002
Recalling firm Apothecary Shoppe
Product type Drugs
Products Estradiol 1.25 mg, Progesterone 25 mg/mL injectable, 20 mL sterile vials, The Apothecary Shoppe, 6136 E. 51st St. Tulsa, OK 74135., SIH-Testosterone Cypionate 200 mg/mL Injectable, 10 mL sterile vial, The Apothecary Shoppe, 6136 E. 51st St. Tulsa, OK 74135.
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Lack of Assurance of Sterility: concerns of sterility assurance with the pharmacy's independent testing laboratory, Lack of Assurance of Sterility: concerns of sterility assurance with the pharmacy's independent testing laboratory.
Initiation date Sep 6, 2013
Report date Oct 9, 2013
Termination date Feb 8, 2016
City Tulsa
State OK
Country United States
FEI number 3001576820

At a glance

  • 1–9 Products in this recall
  • 1–9 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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