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Class II: temporary or reversible health riskTerminated

Magno Humphries Laboratories OPTIMUM E-1000 IU Gluten Free Dietary Recall

OPTIMUM E-1000 IU Gluten Free Dietary Supplement 100 SOFTGELS Product is packaged in…

Magno Humphries Laboratories, Inc · Tigard, OR

Risk level
Class II
Reported by FDA
Apr 23, 2014
Recall ID
F-1821-2014
Check your lot numberHow we source this data

Summary

Magno Humphries Laboratories recalled OPTIMUM E-1000 IU Gluten Free Dietary starting Mar 25, 2014. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1821-2014 on Apr 23, 2014. 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. Status: Terminated.

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.

Product description

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.

Lot numbers, UPCs & expiration codes

343230, 343695, 343788, 344603, and 344936.

Where it was sold

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.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1821-2014
Classification
Class II
Status
Terminated
Recall initiated
Mar 25, 2014
FDA report date
Apr 23, 2014
Quantity
2376 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Magno Humphries Laboratories, Inc

Original FDA data

Every field from FDA enforcement report F-1821-2014, exactly as published.

Show all FDA fields
City
Tigard
State
OR
Status
Terminated
Country
United States
Event ID
67915
Address
8800 Sw Commercial St
Code information
343230, 343695, 343788, 344603, and 344936.
Postal code
97223-6252
Report date
Apr 23, 2014
Product type
Food
Recall number
F-1821-2014
Classification
Class II
Recalling firm
Magno Humphries Laboratories, Inc
Product quantity
2376 bottles
Termination date
Nov 7, 2014
Reason for recall
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.
Voluntary / mandated
Voluntary: Firm initiated
Product description
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.
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.
Recall initiation date
Mar 25, 2014
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Apr 11, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1821-2014, published Apr 23, 2014. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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