12-Bar Variety Pack (RXBAR) – Undeclared Peanut (2018)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
RXBAR: 12-Bar Variety Pack (Blueberry, Chocolate Sea Salt, Mixed Berry, Peanut Butter, Peanut Butter Chocolate), See Best By Date on individual bars as noted in other 12-bar pack, 1.83 oz. per bar
Brand
CHICAGO BAR COMPANY LLC RXBAR
Lot Codes / Batch Numbers
12-Bar Variety Pack (Blueberry, Chocolate Sea Salt, Mixed Berry, Peanut Butter, Peanut Butter Chocolate), UPC 57777 00435, See Best By Date on individual bars as noted in other 12-bar pack
Products Sold
12-Bar Variety Pack (Blueberry, Chocolate Sea Salt, Mixed Berry, Peanut Butter, Peanut Butter Chocolate), UPC 57777 00435, See Best By Date on individual bars as noted in other 12-bar pack
CHICAGO BAR COMPANY LLC RXBAR is recalling RXBAR: 12-Bar Variety Pack (Blueberry, Chocolate Sea Salt, Mixed Berry, Peanut Butter, Peanut Butte due to Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AZ, AR, CA, CO, CT, DE, FL, GA, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, NV, NH, NJ, NY, NC, ND, OH, OK, OR, PA, RI, SC, TN, TX, UT, VT, VA, WA, WI, DC
Page updated: Jan 6, 2026