Reported Jan 22, 2014 · Terminated
SEVELAMER CARBONATE Tablet, 800 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 58468013001
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?
- SEVELAMER CARBONATE Tablet, 800 mg, Rx only
- Distributed byAidaPak Service, LLC, NDC 58468013001
- Lot codes and dates
10 of 10 products
Products covered by this recall # Product as published 1 AD39858_4, EXP: 5/15/2014 2 Pedigree: AD70629_16, EXP: 5/29/2014 3 Pedigree: W002778, EXP: 6/6/2014 4 Pedigree: W002859, EXP: 6/7/2014 5 Pedigree: W003029, EXP: 6/11/2014 6 Pedigree: AD56917_4, EXP: 5/21/2014 7 Pedigree: AD73627_11, EXP: 5/30/2014 8 Pedigree: W002710, EXP: 6/6/2014 9 Pedigree: W002623, EXP: 6/4/2014 10 Pedigree: W003491, EXP: 6/20/2014. - Amount recalled
- 3,238 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; SEVELAMER CARBONATE Tablet, 800 mg may be potentially mislabeled as tiZANidine HCl, Tablet, 2 mg, NDC 55111017915, Pedigree: AD46265_16, EXP: 5/15/2014; LEVOTHYROXINE SODIUM, Tablet, 88 mcg, NDC 00781518392, Pedigree: AD70629_13, EXP: 5/29/2014; QUEtiapine FUMARATE, Tablet, 100 mg, NDC 60505313301, Pedigree: W002777, EXP: 6/6/2014; VALSARTAN, Tablet, 160 mg, NDC 0007803
This product could cause temporary or reversible health problems — stop using it.
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