Reported Jan 22, 2014 · Terminated
guaiFENesin ER Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63824000834
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?
- guaiFENesin ER Tablet, 600 mg, Rx only
- Distributed byAidaPak Service, LLC, NDC 63824000834
- Lot codes and dates
8 of 8 products
Products covered by this recall # Product as published 1 AD62834_4, EXP: 5/24/2014 2 Pedigree: AD62834_7, EXP: 5/24/2014 3 Pedigree: W003514, EXP: 6/21/2014 4 Pedigree: W003574, EXP: 6/24/2014 5 Pedigree: W003850, EXP: 6/27/2014 6 Pedigree: W003931, EXP: 6/28/2014 7 Pedigree: AD46429_1, EXP: 5/15/2014 8 Pedigree: AD73592_1, EXP: 5/31/2014. - Amount recalled
- 480 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; guaiFENesin ER, Tablet, 600 mg may be potentially mislabeled as PRENATAL MULTIVITAMIN/ MULTIMINERAL, Tablet, NDC 51991056601, Pedigree: AD62829_18, EXP: 5/24/2014; guaiFENesin ER, Tablet, 600 mg, NDC 63824000834, Pedigree: AD62834_4, EXP: 5/24/2014; diphenhydrAMINE HCl, Tablet, 25 mg, NDC 00904555159, Pedigree: W003513, EXP: 6/21/2014; DOCUSATE SODIUM, Capsule, 250 mg,
This product could cause temporary or reversible health problems — stop using it.
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