FDAFDA · Food and drugs·Recall number D-1279-2014
Fluoxetine Capsules, USP, 20 mg, 30-count bottles, Rx only, Distributed by: Wal-Mart, Bentonville, AR 72716; Manufactured by: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960; Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045, NDC 68645-130-54, UPC 3 68645 13054 5.
Published May 7, 2014 · Recall initiated: February 14, 2014
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: The recalling firm received notice that their supplier is recalling capsules due to complaints of capsules having an unusual odor.
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Brand
- FLUOXETINE
- Manufacturer
- Legacy Pharmaceutical Packaging
- Distributor
- Nationwide
- UPC
- 0368645130545
- Lot
- Lot numbers: 131328, Exp 08/15; 131634, Exp 09/15; and 131833, Exp 11/15
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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