Reported Jan 29, 2014 · Terminated
NICOTINE POLACRILEX, GUM, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00536302923.
Aidapak Services, LLC
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: Aidapak Services, LLC · 14301 Se 1st St · Vancouver, WA · 98684-3501
Is this the product you have?
- NICOTINE POLACRILEX, GUM, 2 mg, Rx only
- Distributed byAidaPak Service, LLC, NDC 00536302923
- Lot codes and dates
- NICOTINE POLACRILEX, GUM, 2
- mg has the following codesPedigree: AD33897_28
- EXP2/28/2014
- PedigreeW003100
- EXP6/13/2014
- Amount recalled
- 1210 Pieces
This recall covers 265 products
The agency filed one notice per product. You are reading one of them; the other 264 are below.
252 more are in the archive.
Where it was sold
Why it was recalled
Labeling: Label Mixup:NICOTINE POLACRILEX, GUM, 2 mg may have potentially been mislabeled as one of the following drugs: FOLIC ACID, Tablet, 1 mg, NDC 65162036110, Pedigree: AD33897_22, EXP: 5/9/2014; QUEtiapine FUMARATE, Tablet, 25 mg, NDC 60505313001, Pedigree: W003099, EXP: 6/13/2014.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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