Reported Jan 22, 2014 · Terminated
FERROUS SULFATE, Tablet, 325 mg (65 mg Elem Fe), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904759160
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?
- FERROUS SULFATE, Tablet, 325 mg (65 mg Elem Fe), Over The Counter
- Distributed byAidaPak Service, LLC, NDC 00904759160
- Lot codes and dates
- FERROUS SULFATE, Tablet, 325 mg (65 mg Elem
- Fe) has the following codes PedigreeW002717
- EXP6/6/2014
- PedigreeW002826
- EXP6/7/2014
- PedigreeAD60268_1
- EXP5/22/2014
- Amount recalled
- 402 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; FERROUS SULFATE, Tablet, 325 mg (65 mg Elem Fe) may be potentially mislabeled as COENZYME Q-10, Capsule, 100 mg, NDC 37205055065, Pedigree: W002711, EXP: 6/6/2014; VENLAFAXINE HCL, Tablet, 25 mg, NDC 00093019901, Pedigree: W002825, EXP: 12/31/2013; DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375710, Pedigree: AD60236_1, EXP: 5/22/2014.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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