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FDAFDA · Food and drugs·Recall number D-0489-2018

Estradiol Hemihydrate USP (Micronized) (Soy) for prescription compounding, packaged in a) 5g (NDC 58597-8001-3); b) 25g (NDC 58597-8001-5); c)100 g (NDC 58597-8001-6), RX only, packed by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI 48327

Published February 28, 2018 · Recall initiated: February 9, 2018

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
American Pharmaceutical Ingredients LLC
Distributor
Nationwide within USA.
Lot
Lot: #:a) 083017-1, Exp. 7/22/2022; b) 083017-1, Exp. 7/22/2022; c) 083017-1, Exp. 7/22/2022.
Risk classification
Class II
Area (FDA)
drug
Country
United States

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