Food Recall Check
Class I · High risk Terminated Initiated Feb 13, 2013 (14 years ago)

ebA*(TM) Multivitamin Supplement recall

Recalled by Saratoga Therapeutics, LLC · North Wales, PA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

The recall was initiated due to discovery of the presence of milk components (milk protein(s) and lactose) despite labeling that incorrectly states it is free of milk components.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

ebA*(TM) Multivitamin Supplement, 180 tablets in plastic bottles, Distributed by Saratoga Therapeutics, LLC, North Wales, PA.

Quantity: 890 bottles

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 number 0912164, exp 12/12 and 1110354, exp 10/14

Where it was sold

Nationwide.

FDA's distribution note: Product was sold through physicians offices and via internet sales to consumers located nationwide and in Canada.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
Saratoga Therapeutics, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 13, 2013
In FDA report of
Sep 11, 2013
Terminated
Sep 4, 2014
FDA recall number
F-1876-2013 · event 65032
Official record
FDA enforcement report search

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