Nicorette recalls
Nicorette products have been recalled 4 times, most recently on 30 Apr 2014. The recalling company is usually GlaxoSmithKline Consumer Healthcare;. The most common reason is potency & assay.
Total recalls4since 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 30 Apr 2014
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 0 0%Class III 4 100%
Why nicorette is recalled
Companies
Product types
By year
All nicorette recalls, newest first
4 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Nicorette (nicotine polacrilex) Lozenges Mini, 2 mg recalledNicorette | GlaxoSmithKline Consumer Healthcare; | Potency & Assay | Nationwide |
| Drug | CLASS III | Nicotine polacrilex lozenge, 4 mg, Original Flavor cartons recalledNicorette | GlaxoSmithKline Consumer Healthcare; | Potency & Assay | Nationwide |
| Drug | CLASS III | Nicorette (nicotine polacrilex) Lozenges Mini, 4 mg recalledNicorette | GlaxoSmithKline Consumer Healthcare; | Potency & Assay | Nationwide |
| Drug | CLASS III | Nicotine polacrilex lozenge, 2 mg, Original Flavor cartons recalledNicorette | GlaxoSmithKline Consumer Healthcare; | Potency & Assay | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.