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

🇺🇸 United States

1. December 19, 2018 - Recall initiated
2. February 20, 2019 - Reported by source
3. September 29, 2020 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0878-2019

Event ID

81825

Status

Terminated

Classification

Class II

Company

CHICAGO BAR COMPANY LLC RXBAR

Product description

Coconut Chocolate RXBARs , 1.83 oz., single bar, , 12-count carton, 5-count carton, 4-count carton

Quantity

75,695,266 Individually wrapped bars

Reason

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

Recall initiation date

December 19, 2018

Report date

February 20, 2019

Classification date

Not published in this source record

Termination date

September 29, 2020

Distribution pattern

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

UPC, lot, and code information

single bar, UPC 57777 00421, 12-count carton, UPC 57777 00428, 5-count carton, UPC 58030 00844, 4-count carton, UPC 57777 00491 Best By Dates between 3/1/2019 10/13/2019

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 81825 with 10 other product entries in Public Health Trace.

Responsible company: CHICAGO BAR COMPANY LLC RXBAR

Other recalls from CHICAGO BAR COMPANY LLC RXBAR

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Alabama	1
Arkansas	1
Arizona	1
California	1
Colorado	1
Connecticut	1
District of Columbia	1
Delaware	1
Florida	1
Georgia	1
Iowa	1
Idaho	1
Illinois	1
Indiana	1
Kansas	1
Kentucky	1
Louisiana	1
Massachusetts	1
Maryland	1
Maine	1
Michigan	1
Minnesota	1
Missouri	1
Mississippi	1
North Carolina	1
North Dakota	1
New Hampshire	1
New Jersey	1
Nevada	1
New York	1
Ohio	1
Oklahoma	1
Oregon	1
Pennsylvania	1
Rhode Island	1
South Carolina	1
Tennessee	1
Texas	1
Utah	1
Virginia	1
Vermont	1
Washington	1
Wisconsin	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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