FDA recall record

CHICAGO BAR COMPANY LLC RXBAR KIDS Berry Blast, 1.16 oz recall — FDA F-0890-2019

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

Class IIclassification
F-0890-2019official record ID
Feb 20, 2019report date

Recall record at a glance

Official recordF-0890-2019
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCHICAGO BAR COMPANY LLC RXBAR
Report dateFeb 20, 2019
Recall initiation dateDec 19, 2018
Quantity75,695,266 Individually wrapped bars
LocationChicago, IL, United States

Official product description

KIDS Berry Blast, 1.16 oz. bars, single bar, 16-count carton, 5-count carton

Why the product was recalled

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

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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