Reported Jan 29, 2014 · Terminated
DOCUSATE SODIUM, Capsule, 250 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536375701.
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?
- DOCUSATE SODIUM, Capsule, 250 mg, Over The Counter
- Distributed byAidaPak Service, LLC, NDC 00536375701
- Lot codes and dates
9 of 9 products
Products covered by this recall # Product as published 1 Pedigree: AD25452_13, EXP: 5/3/2014 2 Pedigree: AD54498_4, EXP: 5/20/2014 3 Pedigree: AD65457_19, EXP: 5/24/2014 4 Pedigree: W003358, EXP: 6/19/2014 5 Pedigree: W003558, EXP: 6/24/2014 6 Pedigree: AD60211_11, EXP: 5/22/2014 7 Pedigree: W003114, EXP: 6/13/2014 8 Pedigree: AD37063_4, EXP: 5/13/2014 9 Pedigree: AD73652_1, EXP: 5/29/2014. - Amount recalled
- 1204 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: DOCUSATE SODIUM, Capsule, 250 mg may have potentially been mislabeled as one of the following drugs: PIOGLITAZONE, Tablet, 15 mg, NDC 00591320530, Pedigree: AD25452_10, EXP: 4/30/2014; PHOSPHORUS, Tablet, 250 mg, NDC 64980010401, Pedigree: AD54498_1, EXP: 5/20/2014; LACTOBACILLUS GG, Capsule, 0, NDC 49100036374, Pedigree: AD65457_16, EXP: 5/24/2014; guaiFENesin ER, Table
This product could cause temporary or reversible health problems — stop using it.
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