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FDAFDA · Food and drugs·Recall number D-305-2013

Femhrt (norethindrone acetate and ethinyl estradiol) tablets, 1.0 mg/5.0 mcg, 90 count bottle ( NDC#: 0430-0544-23), Rx only, Manufactured by Warner Chilcott Company, LLC, Fajardo, PR 00738, Marketed by Warner Cholcott (US), LLC, Rockaway, NJ 07866

Published May 8, 2013 · Recall initiated: February 15, 2013

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

Chemical contamination: Firm's inspection discovered the presence of 2-phenylphenol in the product due to migration from the cardboard cartons in which the product is packaged.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Warner Chilcott Company LLC
Distributor
US Nationwide and Puerto Rico
Lot
Lot# 507694B; exp 02/13
Risk classification
Class III
Area (FDA)
drug
Country
United States

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