FDA recall record

Mallinckrodt Hydrocodone Bitartrate and Acetaminophen Oral Solution, 7.5 mg/500 mg per 15 recall — FDA D-1431-2012

CGMP Deviations: This product is being recalled because expired flavoring was used in the manufacturing of these lots.

Class IIclassification
D-1431-2012official record ID
Aug 8, 2012report date

Recall record at a glance

Official recordD-1431-2012
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMallinckrodt Inc.
Report dateAug 8, 2012
Recall initiation dateMay 25, 2012
Quantity44,330 bottles
LocationHobart, NY, United States

Official product description

Hydrocodone Bitartrate and Acetaminophen Oral Solution, 7.5 mg/500 mg per 15 mL, 16 fl oz (473 mL) bottle, Rx only, Mallinckrodt Inc., Hazelwood, MO 63042 USA, NDC 0406-0375-16, UPC 3 0406-0375-16 1.

Why the product was recalled

CGMP Deviations: This product is being recalled because expired flavoring was used in the manufacturing of these lots.

Distribution information

Nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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