Menu
FDA · Food recall

OPTIMUM E-1000 IU Gluten Free Dietary Supplement 100 SOFTGELS Product is packaged in a white HDPE bottle with…

April 23, 2014 Class II

Date
April 23, 2014
Risk class
Class II (FDA's definition, 21 CFR 7.3(m): a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote)
Status
Terminated
Filed by
Magno Humphries Laboratories, Inc
Product
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.
Reason
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.
Distribution pattern
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.
Quantity
2376 bottles
Codes and lots
343230, 343695, 343788, 344603, and 344936.
Recall started
March 25, 2014
Recall number
F-1821-2014

What should I do? Food recall: what to do with it

Source: FDA · Food enforcement report, recall number F-1821-2014. The agency record governs; check it and the company before acting.

Report a mistake on this page