Reported Jan 22, 2014 · Terminated

MELATONIN Tablet, 3 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 51991001406

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?

  • MELATONIN Tablet, 3 mg, Over The Counter
  • Distributed byAidaPak Service, LLC, NDC 51991001406
Lot codes and dates

6 of 6 products

Products covered by this recall
#Product as published
1AD25452_16, EXP: 5/3/2014
2Pedigree: AD28322_7, EXP: 5/6/2014
3Pedigree: AD70655_14, EXP: 5/28/2014
4Pedigree: W003999, EXP: 7/1/2014
5Pedigree: AD32325_7, EXP: 5/9/2014
6Pedigree: AD68019_7, EXP: 5/28/2014.
Amount recalled
718 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; MELATONIN Tablet, 3 mg may be potentially mislabeled as DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375701, Pedigree: AD25452_13, EXP: 5/3/2014; PIOGLITAZONE, Tablet, 15 mg, NDC 00591320530, Pedigree: AD28322_4, EXP: 4/30/2014; COENZYME Q-10, Capsule, 100 mg, NDC 37205055065, Pedigree: AD70655_11, EXP: 5/28/2014; COENZYME Q-10, Capsule, 100 mg, NDC 37205055065, 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, 6:32 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.