Reported Jan 29, 2014 · Terminated
DULoxetine HCl DR, Capsule, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00002323560.
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?
- DULoxetine HCl DR, Capsule, 20 mg, Rx only
- Distributed byAidaPak Service, LLC, NDC 00002323560
- Lot codes and dates
8 of 8 products
Products covered by this recall # Product as published 1 Pedigree: AD30140_31, EXP: 5/7/2014 2 Pedigree: AD54587_4, EXP: 5/21/2014 3 Pedigree: AD70585_16, EXP: 5/29/2014 4 Pedigree: W003506, EXP: 6/21/2014 5 Pedigree: AD60272_61, EXP: 5/22/2014 6 Pedigree: AD21790_49, EXP: 5/1/2014 7 Pedigree: W003005, EXP: 6/11/2014 8 Pedigree: W003486, EXP: 6/20/2014. - Amount recalled
- 600 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: DULoxetine HCl DR, Capsule, 20 mg, may be potentially mis-labeled with one of the following drugs: ENTECAVIR, Tablet, 0.5 mg, NDC 00003161112, Pedigree: AD30140_28, EXP: 5/7/2014; CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: AD54587_1, EXP: 5/21/2014; FLUoxetine HCl, Capsule, 10 mg , NDC 16714035103, Pedigree: AD70585_13, EXP: 5/29/2014; CHOLECALCIFEROL
This product could cause temporary or reversible health problems — stop using it.
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