Reported Jan 22, 2014 · Terminated
DOCUSATE SODIUM, Capsule, 250 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904789159
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 00904789159
- Lot codes and dates
7 of 7 products
Products covered by this recall # Product as published 1 AD68028_1, EXP: 5/28/2014 2 Pedigree: AD68022_1, EXP: 5/28/2014 3 Pedigree: AD37072_1, EXP: 5/13/2014 4 Pedigree: AD37072_4, EXP: 5/13/2014 5 Pedigree: AD56924_1, EXP: 5/21/2014 6 Pedigree: W003671, EXP: 6/25/2014 7 Pedigree: W002920, EXP: 6/10/2014. - Amount recalled
- 4,318 Capsules
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; DOCUSATE SODIUM, Capsule, 250 mg may be potentially mislabeled as ATROPINE SULFATE/DIPHENOXYLATE HCL, Tablet, 0.025 mg/2.5 mg, NDC 00378041501, Pedigree: AD65475_13, EXP: 5/28/2014; VALSARTAN, Tablet, 80 mg, NDC 00078035834, Pedigree: AD68025_1, EXP: 5/28/2014; PANTOPRAZOLE SODIUM DR, Tablet, 40 mg, NDC 64679043402, Pedigree: AD37063_10, EXP: 5/13/2014; DOCUSATE SODIUM
This product could cause temporary or reversible health problems — stop using it.
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