Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 25, 2014 (13 years ago)

OPTIMUM E-1000 IU Gluten Free Dietary Supplement 100 SOFTGELS… recall

Recalled by Magno Humphries Laboratories, Inc · Tigard, OR, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Magno Humphries Laboratories is recalling Vitamin E softgels because the principle display panel states the product contains 1000 IU of Vitamin E however the Supplement Facts label indicated 200 IU of Vitamin E. The supplement actually contains 1000 IU of Vitamin E.

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

OPTIMUM E-1000 IU Gluten Free Dietary Supplement 100 SOFTGELS Product is packaged in a white HDPE bottle with foil cap under the white plastic cap. Bottle contains 100 softgel caps. UPC 0 43292 56291 7.

Quantity: 2376 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.

343230, 343695, 343788, 344603, and 344936.

Where it was sold

Nationwide.

Alabama California Colorado Florida Georgia Illinois Massachusetts Missouri North Carolina New York Ohio Texas Washington

FDA's distribution note: One consignee - Medline Industries, Inc. HQ located in IL One Medline Place, Mundelein, Illinois 60060 1-800-MEDLINE. Products distributed Nationwide (AL, CA, CO,FL, GA, IL, MA, MO, NC, NY, OH, TX, and WA) to Medline Industries distribution centers.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
Magno Humphries Laboratories, Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 25, 2014
In FDA report of
Apr 23, 2014
Terminated
Nov 7, 2014
FDA recall number
F-1821-2014 · event 67915
Official record
FDA enforcement report search

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