RECALL RECORD — CLASS IIRecall closedF-0888-2019/FDA enforcement

Rxbar: Mixed Berry, Single Bar, 12-count Carton

What you need to know

Class II
  • What happened

    Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. 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 FDAAL, AR, AZ, CA +39 moreMore food

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Product identification

Source: FDA FOOD

Brand nameChicago Bar Company LLC Rxbar
Recalling firmChicago Bar Company LLC RxbarChicago, IL, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Mixed Berry, single bar, UPC 57777 00467, 12-count carton, UPC 57777 00470, 4-count carton, UPC 59162 00700 Best By Dates between 3/14/2019 5/6/2019 and 7/10/2019 8/30/2019
Distribution area
ALARAZCACOCTDCDEFLGAIAIDILINKSKYLAMAMDMEMIMNMOMSNCNDNHNJNVNYOHOKORPARISCTNTXUTVAVTWAWI

Domestic:AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI Foreign: The firm did not report any foreign distribution DOD: NV, VA

United States

Quantity affected75, 695, 266 Individually wrapped bars
Recall initiationFDA report date: February 20, 2019
FDA recall numberF-0888-2019

Beyond the headline

The recall, in context

Chicago Bar Company LLC Rxbar initiated this food recall on December 19, 2018. The FDA enforcement report states: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut. The FDA report lists distribution as: Domestic:AL, AR, AZ,CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI Foreign: The firm did not report any foreign distribution DOD: NV, VA.

The FDA enforcement report describes the reason as: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.

Rxbar: Mixed Berry, Single Bar, 12-count Carton was made or distributed by Chicago Bar Company LLC Rxbar in Chicago, IL, United States. This page reflects FDA report F-0888-2019, dated February 20, 2019.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. 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 may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

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 peanut

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a peanut 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 peanut allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a peanut 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 Rxbar: Mixed Berry, Single Bar, 12-count Carton recall?

Chicago Bar Company LLC Rxbar recalled Rxbar: Mixed Berry, Single Bar, 12-count Carton in an FDA Class II enforcement action reported as F-0888-2019. Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.

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 peanut 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.

Is the Chicago Bar Company LLC Rxbar 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-0888-2019. 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 Chicago Bar Company LLC Rxbar

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