Reported Jan 22, 2014 · Terminated
QUEtiapine FUMARATE Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505313301
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?
- QUEtiapine FUMARATE Tablet, 100 mg, Rx only
- Distributed byAidaPak Service, LLC, NDC 60505313301
- Lot codes and dates
- QUEtiapine FUMARATE, Tablet, 100
- mg has the following codes PedigreeW002777
- EXP6/6/2014
- PedigreeW003825
- EXP6/27/2014
- PedigreeAD73623_13
- EXP5/30/2014
- Amount recalled
- 1,300 Tablets
This recall covers 273 products
The agency filed one notice per product. You are reading one of them; the other 272 are below.
260 more are in the archive.
Where it was sold
Why it was recalled
Labeling:Label Mixup; QUEtiapine FUMARATE Tablet, 100 mg may be potentially mislabeled as DOCUSATE CALCIUM, Capsule, 240 mg, NDC 00536375501, Pedigree: W002776, EXP: 6/6/2014; NICOTINE POLACRILEX, Lozenge, 2 mg, NDC 37205098769, Pedigree: W003823, EXP: 6/27/2014; DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375710, Pedigree: AD60578_5, EXP: 5/29/2014.
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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