Reported Feb 5, 2014 · Terminated

Hydrocodone Bitartrate and Acetaminophen Tablets USP, CIII, 10 mg/ 660 mg, 100 count bottles, Rx only. Manufactured by…

Watson Laboratories Inc.

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: Watson Laboratories Inc · 132 Business Center Dr · Corona, CA · 92880-1724

Is this the product you have?

  • Hydrocodone Bitartrate and Acetaminophen Tablets USP, CIII, 10 mg/ 660 mg, 100 count bottles, Rx only. Manufactured by Watson Laboratories, Inc., Corona, CA 92880
  • Distributed byWatson Pharma, Inc
  • NDC00591-0517-01
Lot codes and dates
  • Lot #: 697316A
  • ExpiryMar 2015
Amount recalled
717 bottles

Where it was sold

Why it was recalled

Failed Tablet/Capsule Specifications; Product contains broken tablets.

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 Jul 25, 2014 · Data as of Sep 19, 7:50 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.