Recalls / Class III
Class IIID-305-2013
Product
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
- Affected lot / code info
- Lot# 507694B; exp 02/13
Why it was recalled
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.
Recalling firm
- Firm
- Warner Chilcott Company LLC
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- Road 195, Km 1.1, Union Street, Fajardo, Puerto Rico 00738
Distribution
- Quantity
- 6,408 bottles
- Distribution pattern
- US Nationwide and Puerto Rico
Timeline
- Recall initiated
- 2013-02-15
- FDA classified
- 2013-04-30
- Posted by FDA
- 2013-05-08
- Terminated
- 2014-06-09
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-305-2013. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.