RECALL RECORD — CLASS IIIRecall closedF-1862-2017/FDA enforcement
Mcshare's INC·Food·Mar 11, 2017

Ixl Advanced Performance Matrix, Nutritional Premix, NET WT

What you need to know

Class III
  • What happened

    Product manufactured with an ingredient that contains low levels of soy; soy is not declared on product label.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall closed · classified by the FDAIN, MO, TXMore food

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Product identification

Source: FDA FOOD

Brand nameMcshare's INC
Recalling firmMcshare's INCSalina, KS, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot numbers and Expiration dates: IXL-180516-20, 5/18/2017 IXL-180516-21, 5/18/2017 IXL-210117-50, 1/21/2018
Distribution area
INMOTX

Product was distributed for further manufacturing to customers in MO and TX.

United States

Quantity affected3600 lbs.
Recall initiationFDA report date: April 12, 2017
FDA recall numberF-1862-2017

Beyond the headline

The recall, in context

Mcshare's INC initiated this food recall on March 11, 2017. The FDA enforcement report states: Product manufactured with an ingredient that contains low levels of soy; soy is not declared on product label. The FDA report lists distribution as: Product was distributed for further manufacturing to customers in MO and TX.

The FDA enforcement report describes the reason as: Product manufactured with an ingredient that contains low levels of soy; soy is not declared on product label.

Ixl Advanced Performance Matrix, Nutritional Premix, NET WT was made or distributed by Mcshare's INC in Salina, KS, United States. This page reflects FDA report F-1862-2017, dated April 12, 2017.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared soy

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a soy allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed soy allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a soy allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Ixl Advanced Performance Matrix, Nutritional Premix, NET WT recall?

Mcshare's INC recalled Ixl Advanced Performance Matrix, Nutritional Premix, NET WT in an FDA Class III enforcement action reported as F-1862-2017. Product manufactured with an ingredient that contains low levels of soy; soy is not declared on product label.

What are the symptoms of Undeclared soy exposure?

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a soy allergy.

How quickly can Undeclared soy symptoms appear?

Reactions can begin within minutes to a few hours after eating the product.

Who is most at risk from Undeclared soy?

People with a diagnosed soy allergy, especially children and anyone with a history of anaphylaxis.

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have a soy allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

How do I get a refund from Mcshare's INC?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-1862-2017 and keep the packaging, lot code and proof of purchase if you have them.

Is the Mcshare's INC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1862-2017. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.