US Drug Recall Register
Class III · Low risk Terminated Initiated Feb 20, 2014 (13 years ago)

Nicorette Lozenge, Nicoderm CQ, and Nicorette Gum nicotine polacrilex combination…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.

What was recalled

Nicorette Lozenge, Nicoderm CQ, and Nicorette Gum nicotine polacrilex combination. Contains 30 Pieces/ Pallet. OTC only. GlaxoSmithKlein, 1000 GSK Drive, Moon Township, PA 15108. UPC: 0-03-0766-1442-81-2.

Recalling firm
GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline
Origin
SC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1244-2014

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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