Reported May 7, 2014 · Terminated

Fluoxetine Capsules, USP, 20 mg, 30-count bottles, Rx only, Distributed by

Legacy Pharmaceutical Packaging

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Legacy Pharmaceutical Packaging · 13333 Lakefront Dr · Earth City, MO · 63045-1514

Is this the product you have?

Fluoxetine Capsules, USP, 20 mg, 30-count bottles, Rx only, Distributed by

3 of 3 products

Products covered by this recall
#Product as published
1Wal-Mart, Bentonville, AR 72716
2Manufactured by: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960
3Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045, NDC 68645-130-54, UPC 3 68645 13054 5.
Lot codes and dates
  • Lot numbers
    • 131328
    • Exp 08/15
    • 131634
    • Exp 09/15
    • and 131833
    • Exp 11/15
Amount recalled
667,068 bottles

Where it was sold

  • Nationwide

Why it was recalled

Chemical Contamination: The recalling firm received notice that their supplier is recalling capsules due to complaints of capsules having an unusual odor.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Nov 27, 2017 · Data as of Sep 19, 7:54 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.