Reported Jan 22, 2014 · Terminated
FAMOTIDINE Tablet, 20 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 16714036104
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?
- FAMOTIDINE Tablet, 20 mg, Over The Counter
- Distributed byAidaPak Service, LLC, NDC 16714036104
- Lot codes and dates
5 of 5 products
Products covered by this recall # Product as published 1 W003226, EXP: 6/17/2014 2 Pedigree: W003507, EXP: 6/21/2014 3 Pedigree: W003508, EXP: 6/21/2014 4 Pedigree: W003764, EXP: 6/26/2014 5 Pedigree: W003406, EXP: 6/19/2014. - Amount recalled
- 700 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; FAMOTIDINE Tablet, 20 mg may be potentially mislabeled as CARVEDILOL PHOSPHATE ER, Capsule, 20 mg, NDC 00007337113, Pedigree: W003225, EXP: 6/17/2014; DULoxetine HCl DR, Capsule, 20 mg, NDC 00002323560, Pedigree: W003506, EXP: 6/21/2014; FAMOTIDINE, Tablet, 20 mg, NDC 16714036104, Pedigree: W003507, EXP: 6/21/2014; MYCOPHENOLATE MOFETIL, Capsule, 250 mg, NDC 0037822500
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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