Class II · Moderate risk Terminated
REMfresh Advanced Ion-Powered Melatonin
Reason cGMP deviations
Melatonin
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Labeling:Label Mixup; MELATONIN, Tablet, 1 mg may be potentially mislabeled as OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 40985022921, Pedigree: W003711, EXP: 6/26/2014.
What was recalled
MELATONIN, Tablet, 1 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 74312002832
- Recalling firm
- Aidapak Services, LLC
- Origin
- WA, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-734-2014
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Melatonin recalls
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Class II · Moderate risk Terminated
REMfresh Advanced Ion-Powered Melatonin
Reason cGMP deviations
Class II · Moderate risk Terminated
MidNite Natural sleep aid Chewable Tablets Cherry Flavor
Reason cGMP deviations
Class II · Moderate risk Terminated
CVS Health Natural Sleep Aid Chewable Tablets Cherry Flavor
Reason cGMP deviations
Class II · Moderate risk Terminated
Lite Remfresh Advanced Ion-Powered Melatonin
Reason cGMP deviations
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