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RECALL RECORD — CLASS IRecall closedF-1166-2022/FDA enforcement
Liberty Fruit Co INC Dba Carol's Cuts·Food·May 6, 2022

Potato 1/4" Dice 4/5# C/c (01)10886810715535(10)0016088723 71553 Best If Used by: 04/06/22…

What you need to know

Class I

  • What happened

    Sodium metabisulfite not declared on product label.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. 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 FDAINMore food

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Product identification

Source: FDA FOOD

Brand nameLiberty Fruit Co INC Dba Carol's Cuts
Recalling firmLiberty Fruit Co INC Dba Carol's CutsKansas City, KS, United States
UPC / barcodes
10 886810 71553 5
Lot / date codes
  • Best if used by: 04/06/22 Product #: 71553
Distribution area
IN

Distributed to food service locations in Kansas, Nebraska, Iowa, and Missouri.

United States

Quantity affected25, 433 lbs (total)
Recall initiationFDA report date: June 15, 2022
FDA recall numberF-1166-2022

Beyond the headline

The recall, in context

Liberty Fruit Co INC Dba Carol's Cuts initiated this food recall on May 6, 2022. The FDA enforcement report states: Sodium metabisulfite not declared on product label. The FDA report lists distribution as: Distributed to food service locations in Kansas, Nebraska, Iowa, and Missouri.

The FDA enforcement report describes the reason as: Sodium metabisulfite not declared on product label.

Potato 1/4" Dice 4/5# C/c (01)10886810715535(10)0016088723 71553 Best If Used by: 04/06/22… was made or distributed by Liberty Fruit Co INC Dba Carol's Cuts in Kansas City, KS, United States. This page reflects FDA report F-1166-2022, dated June 15, 2022.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. 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 has a reasonable probability of causing serious adverse health consequences or death.

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 UPC and lot code 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 allergen

Symptoms to watch for

Hives, swelling, wheezing, coughing, vomiting, abdominal pain or a drop in blood pressure. Anaphylaxis is a medical emergency.

When symptoms may appear

Allergic reactions often begin within minutes to a few hours of eating the allergen.

Higher-risk groups

Anyone with a diagnosed food allergy, especially children, and people with a history of anaphylaxis or asthma.

What to do now

  1. 1Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy.
  2. 2If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services.
  3. 3Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

For a severe allergic reaction, do not wait for a callback or refund process before seeking emergency care.

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 Potato 1/4" Dice 4/5# C/c (01)10886810715535(10)0016088723 71553 Best If Used by: 04/06/22… recall?

Liberty Fruit Co INC Dba Carol's Cuts recalled Potato 1/4" Dice 4/5# C/c (01)10886810715535(10)0016088723 71553 Best If Used by: 04/06/22… in an FDA Class I enforcement action reported as F-1166-2022. Sodium metabisulfite not declared on product label.

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 or serve the affected product if you or anyone in the household has a diagnosed allergy. If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services. Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

Is the Liberty Fruit Co INC Dba Carol's Cuts 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-1166-2022. 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

More recalls by Liberty Fruit Co INC Dba Carol's Cuts

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Class I·

Liberty Fruit Co INC Dba Carol's Cuts

Potato Yukon W/skin 1/16"4/5 a (01)10886810715412(10)0016088347 71541 Best If Used by: …

Sodium metabisulfite not declared on product label.

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Class I·

Liberty Fruit Co INC Dba Carol's Cuts

Potato a Reddice1/2"4/5#w/skin (01)10886810715269(10)0016088725 71526 Best If Used by: 04/26/22…

Sodium metabisulfite not declared on product label.

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