FDA recall record

Empower Pharmacy, Estradiol Cypionate Injection, 10mg/mL, 5mL Sterile Multiple Dose Vial recall — FDA D-0630-2024

Lack of Assurance of Sterility

Class IIclassification
D-0630-2024official record ID
Aug 14, 2024report date

Recall record at a glance

Official recordD-0630-2024
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmEMPOWER CLINIC SERVICES LLC
Report dateAug 14, 2024
Recall initiation dateAug 2, 2024
Quantity2,797
LocationHouston, TX, United States

Official product description

Empower Pharmacy, Estradiol Cypionate Injection, 10mg/mL, 5mL Sterile Multiple Dose Vial, For IM or SQ use only, RX only, Compounded by: Empower Pharmacy 7601 N Sam Houston Pkwy W Ste 100, Houston, TX 77064

Why the product was recalled

Lack of Assurance of Sterility

Distribution information

Nationwide within the United States

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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