Reported Jan 22, 2014 · Terminated
MIRTAZAPINE Tablet, 7.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762141503
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?
- MIRTAZAPINE Tablet, 7.5 mg, Rx only
- Distributed byAidaPak Service, LLC, NDC 59762141503
- Lot codes and dates
- MIRTAZAPINE, Tablet, 7.5
- mg has the following codes PedigreeAD73525_55
- EXP5/30/2014
- PedigreeW003012
- EXP6/11/2014
- PedigreeW003334
- EXP6/18/2014
- Amount recalled
- 91 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; MIRTAZAPINE Tablet, 7.5 mg may be potentially mislabeled as BROMOCRIPTINE MESYLATE, Tablet, 2.5 mg, NDC 00574010603, Pedigree: AD73525_40, EXP: 5/30/2014; DULoxetine HCl DR, Capsule, 20 mg, NDC 00002323560, Pedigree: W003005, EXP: 6/11/2014; carBAMazepine ER, Tablet, 100 mg, NDC 00078051005, Pedigree: W003330, EXP: 6/18/2014.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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