Class IITerminated in FDA datasetDec 19, 2018

RXBAR: Mixed Berry, single bar

Recalling firm: CHICAGO BAR COMPANY LLC RXBAR

Why it was recalled

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

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The exact product

RXBAR: Mixed Berry, single bar, 12-count carton, UPC 57777 00470, 4-count carton

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Original FDA code information

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

Recall details

Recall number
F-0888-2019
Event ID
81825
FDA status
Terminated
Initiated
Dec 19, 2018
Reported
Feb 20, 2019
Classified
Feb 12, 2019
Terminated
Sep 29, 2020
Quantity
75,695,266 Individually wrapped bars
Location
Chicago, IL, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

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

FDA source record · F-0888-2019

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.