Reported Jan 29, 2014 · Terminated
DUTASTERIDE, Capsule, 0.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00173071215.
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?
- DUTASTERIDE, Capsule, 0.5 mg, Rx only
- Distributed byAidaPak Service, LLC, NDC 00173071215
- Lot codes and dates
- DUTASTERIDE, Capsule, 0.5
- mg has the following codesPedigree: AD49610_1
- EXP5/16/2014
- PedigreeAD70633_1
- EXP5/29/2014
- PedigreeAD52778_4
- EXP5/20/2014
- Amount recalled
- 90 Capsules
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: DUTASTERIDE, Capsule, 0.5 mg may have potentially been mislabeled as one of the following drugs: PHENOL, LOZENGE, 29 mg, NDC 00068021918, Pedigree: AD49582_13, EXP: 5/16/2014; REPAGLINIDE, Tablet, 2 mg, NDC 00169008481, Pedigree: AD70639_13, EXP: 5/29/2014; CHOLECALCIFEROL, Capsule, 5000 units, NDC 00904598660, Pedigree: AD52993_22, EXP: 5/20/2014.
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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