Reported Jan 22, 2014 · Terminated
guaiFENesin ER, Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63824000815
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 63824000815
- Lot codes and dates
6 of 6 products
Products covered by this recall # Product as published 1 AD21965_22, EXP: 5/1/2014 2 Pedigree: AD56917_13, EXP: 5/21/2014 3 Pedigree: AD73627_23, EXP: 5/30/2014 4 Pedigree: W003218, EXP: 6/17/2014 5 Pedigree: W003360, EXP: 6/19/2014 6 Pedigree: W002660, EXP: 6/5/2014. - Amount recalled
- 600 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 MISOPROSTOL, Tablet, 200 mcg, NDC 59762500801, Pedigree: AD21965_13, EXP: 5/1/2014; TACROLIMUS, Capsule, 1 mg, NDC 00781210301, Pedigree: AD56917_7, EXP: 5/21/2014; LACTOBACILLUS GG, Capsule, NDC 49100036374, Pedigree: AD73627_17, EXP: 5/30/2014; LACTOBACILLUS GG, Capsule, NDC 49100036374, Pedigree: W003216
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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