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FDAFDA · Food and drugs·Recall number D-1061-2013

Hydrocodone Bitartrate and Acetaminophen Tablets, 7.5 mg/650 mg Tablets, 500 Count Bottle, Manufactured by: Watson Laboratories, Inc, Cocona, CA 92880, NDC 0591-2611-05.

Published September 25, 2013 · Recall initiated: August 30, 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

Defective Container: Defective bottles may not have tamper evident seals properly seated, and therefore it may be difficult to determine if the product had been opened or tampered with.

What to do

Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Recall details

Manufacturer
Watson Laboratories Inc
Distributor
Nationwide
Lot
Lot 706224A and 706225A, Exp. 04/15.
Risk classification
Class III
Area (FDA)
drug
Country
United States

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