Reported Jan 22, 2014 · Terminated

RANOLAZINE ER Tablet, 500 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 61958100301

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?

  • RANOLAZINE ER Tablet, 500 mg, Rx only
  • Distributed byAidaPak Service, LLC, NDC 61958100301
Lot codes and dates

8 of 8 products

Products covered by this recall
#Product as published
1AD23087_1, EXP: 5/2/2014
2Pedigree: AD62995_7, EXP: 5/29/2014
3Pedigree: W002857, EXP: 6/7/2014
4Pedigree: W003538, EXP: 6/21/2014
5Pedigree: W003741, EXP: 6/26/2014
6Pedigree: AD32757_47, EXP: 5/13/2014
7Pedigree: W003648, EXP: 6/25/2014
8Pedigree: AD60272_40, EXP: 5/22/2014.
Amount recalled
840 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; RANOLAZINE ER Tablet, 500 mg may be potentially mislabeled as MELATONIN, Tablet, 3 mg, NDC 51991001406, Pedigree: AD25452_16, EXP: 5/3/2014; DULoxetine HCl DR, Capsule, 20 mg, NDC 00002323560, Pedigree: AD70585_16, EXP: 5/29/2014; OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 00904404360, Pedigree: W002852, EXP: 6/7/2014; VALSARTAN, Tablet, 80 mg, NDC 00078035834, Pedigree:

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Feb 7, 2014 · Data as of Sep 19, 6:29 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.