FDA recall record
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 softg...
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of November 7, 2014. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
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.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
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.
Code information listed by FDA
343230, 343695, 343788, 344603, and 344936.
Distribution and firm information
Recalling firm listed by FDA: Magno Humphries Laboratories, Inc
Firm location listed by FDA: Tigard, OR, United States
Distribution reported by FDA: 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.
Product quantity listed by FDA: 2376 bottles
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.