Reported Jan 29, 2014 · Terminated
VALSARTAN, Tablet, 160 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00078035934.
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?
- VALSARTAN, Tablet, 160 mg, Rx only
- Distributed byAidaPak Service, LLC, NDC 00078035934
- Lot codes and dates
9 of 9 products
Products covered by this recall # Product as published 1 Pedigree: AD39858_1, EXP: 5/16/2014 2 Pedigree: AD46312_7, EXP: 5/16/2014 3 Pedigree: AD49414_7, EXP: 5/17/2014 4 Pedigree: W002767, EXP: 6/6/2014 5 Pedigree: W003534, EXP: 6/21/2014 6 Pedigree: W003639, EXP: 6/25/2014 7 Pedigree: W002851, EXP: 6/7/2014 8 Pedigree: AD62995_1, EXP: 5/28/2014 9 Pedigree: W002964, EXP: 6/11/2014. - Amount recalled
- 1260 Tablets
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: VALSARTAN, Tablet, 160 mg may have potentially been mislabeled as one of the following drugs: PROGESTERONE, Capsule, 100 mg, NDC 00032170801, Pedigree: AD46320_1, EXP: 5/15/2014; CapsuleTOPRIL, Tablet, 6.25 mg (1/2 of 12.5 mg), NDC 00143117101, Pedigree: AD46312_4, EXP: 5/16/2014; MYCOPHENOLATE MOFETIL, Tablet, 500 mg, NDC 00004026001, Pedigree: AD49414_4, EXP: 5/17/2014;
This product could cause temporary or reversible health problems — stop using it.
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