Food Recall Check
Class III · Low risk Terminated Initiated Jan 12, 2015 (12 years ago)

Melatonin Control- Released Tablets recall

Recalled by Hvl, LLC · Pittsburgh, PA, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Bottles contained a vegetarian digestive enzyme dietary supplement instead of melatonin.

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

Melatonin Control- Released Tablets, 60 tablets, in plastic bottles, Manufactured by Douglas Laboratories, Pittsburgh, PA.

Quantity: 278

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot # 50032151, exp. 12/20/2015

Where it was sold

Nationwide.

FDA's distribution note: Nationwide

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Hvl, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 12, 2015
In FDA report of
Feb 18, 2015
Terminated
Jul 28, 2015
FDA recall number
F-1202-2015 · event 70272
Official record
FDA enforcement report search

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