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FDA FOOD RECALLS

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Every FDA food recall since 2012, in one place. We check each recall's status with FDA every day.

Checked with FDA daily ยท Source: U.S. Food and Drug Administration

7,366 ended recalls ยท showing 2,761 to 2,780

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  1. ENDEDClass I ยท Most seriousRecalled Jan 11, 2019

    El Guapo Pasilla-Ancho Chile Pods 2oz, 7.5oz, 11oz

    Mojave Foods Corporation (subsidiary of McCormick) is initiating a voluntary recall of El Guapo Chile Habanero and Chile Pasilla-Ancho pouches due to ...

    McCormick & Company, Inc. - Flavor Manufacturing Center ยท Hunt Valley, MD

    Where it was sold: Product distributed to the following states: AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN, IA, KS, KY, MI, MN, MO, MT, NE, NV, NM, NC, OH, OK, OR, TN, TX, UT, WI

    UPC 044989010391UPC 044989211088UPC 044989211149
    Show details
    Product, as FDA describes it
    El Guapo Pasilla-Ancho Chile Pods 2oz, 7.5oz, 11oz
    Reason, in FDA's words
    Mojave Foods Corporation (subsidiary of McCormick) is initiating a voluntary recall of El Guapo Chile Habanero and Chile Pasilla-Ancho pouches due to unlabeled peanut allergen.
    Codes on the package
    2oz: UPC# 044989010391; Best By Jun/20/20 7.5oz: UPC# 044989211088; Best By Jun/13/20; Best By Jun/14/20 11oz: UPC# 044989211149; Best By Jun/12/20
    Where it was sold
    Product distributed to the following states: AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN, IA, KS, KY, MI, MN, MO, MT, NE, NV, NM, NC, OH, OK, OR, TN, TX, UT, WI
    Amount recalled
    2 oz, 22,848 pouches ; 7.5oz, 13,896 pouches ; 11oz, 2,064 pouches
    Status
    Ended Jun 27, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1346-2019
  2. ENDEDClass I ยท Most seriousRecalled Jan 3, 2019

    Clancy's Wavy Potato Chips, 10 oz., UPC 0 41498 16306 8

    Product may contain undeclared allergen milk.

    Olde York Potato Chips ยท Fort Wayne, IN

    Where it was sold: Domestic only: OH, NY, PA, WV

    UPC 041498163068
    Show details
    Product, as FDA describes it
    Clancy's Wavy Potato Chips, 10 oz., UPC 0 41498 16306 8
    Reason, in FDA's words
    Product may contain undeclared allergen milk.
    Codes on the package
    BEST If Used By FEB 22 19 1A6
    Where it was sold
    Domestic only: OH, NY, PA, WV
    Amount recalled
    96 cases (960 retail units)
    Status
    Ended May 13, 2019 (FDA lists it as terminated)
    FDA recall number
    F-0815-2019
  3. ENDEDClass II ยท ModerateRecalled Jan 3, 2019

    Snak Club Tajin Chili & Lime Peanuts Mild 5 oz. Produced By: Century Snacks Commerice, CA 90040 ...

    Undeclared allergen; tree nuts.

    Century Snacks LLC ยท Commerce, CA

    Where it was sold: U.S. distribution to the following: AZ, CA, GA, NC, OR, TX. No foreign distribution.

    UPC 087076216405
    Show details
    Product, as FDA describes it
    Snak Club Tajin Chili & Lime Peanuts Mild 5 oz. Produced By: Century Snacks Commerice, CA 90040 centurysnacks.com UPC 0 87076 21640 5
    Reason, in FDA's words
    Undeclared allergen; tree nuts.
    Codes on the package
    Best By AUG 06 2019 TPC2CT
    Where it was sold
    U.S. distribution to the following: AZ, CA, GA, NC, OR, TX. No foreign distribution.
    Amount recalled
    25 packages
    Status
    Ended Mar 13, 2019 (FDA lists it as terminated)
    FDA recall number
    F-0823-2019
  4. ENDEDClass I ยท Most seriousRecalled Dec 28, 2018

    The Forest Wild Collection Dark Chocolate bar, CB15052, net wt. 1.25 oz per bar. Product is packaged...

    The 1.25 oz Forest Wild Wolf Dark Chocolate bars are recalled due to undeclared milk

    Salmon River Foods Inc ยท Boise, ID

    Where it was sold: MA and WI

    Show details
    Product, as FDA describes it
    The Forest Wild Collection Dark Chocolate bar, CB15052, net wt. 1.25 oz per bar. Product is packaged in a card board box of 12 individually wrapped chocolate bars. Dream Chocolate brand, UPC on each bar is 6 76181 15088 1. Label has the wolf image. The label is read in parts: "***INGREDIENTS: Dark Chocolate (sugar, cocoa liquor, cocoa butter, lecithin - an emulsifier and pure vanilla). CONTAINS: Soy.***This product is manufactured at a plant that processes nut and peanuts***2127 Century Way, Boise, Idaho 83709***".
    Reason, in FDA's words
    The 1.25 oz Forest Wild Wolf Dark Chocolate bars are recalled due to undeclared milk
    Codes on the package
    Lot codes S138 and JY238. However these codes are not printed on labels so consumers would not see these codes.
    Where it was sold
    MA and WI
    Amount recalled
    3 boxes each containing 12/1.25 oz dark chocolate bars
    Status
    Ended Aug 12, 2019 (FDA lists it as terminated)
    FDA recall number
    F-0860-2019
  5. ENDEDClass I ยท Most seriousRecalled Dec 20, 2018

    Nutty Choco Pop, 10 oz. bag. Sold in the following configurations: Item #101, Gift Box (contains 1...

    Nutty Choco Pop has in incorrect label and does not declare that it contains cashews and almonds.

    Funky Chunky LLC ยท Eden Prairie, MN

    Where it was sold: Nationwide

    Show details
    Product, as FDA describes it
    Nutty Choco Pop, 10 oz. bag. Sold in the following configurations: Item #101, Gift Box (contains 1-10 oz. bag), Item #1728 Holiday Crowd Pleaser (contains 5-10 oz. bags), and #9676 Crowd Pleaser (contains 5-10 oz. bags).
    Reason, in FDA's words
    Nutty Choco Pop has in incorrect label and does not declare that it contains cashews and almonds.
    Codes on the package
    Item #101, Lot Code 8K30. Item #1728, Lot Code8K20. Item #9676, Lot Codes 8K13, 8K27, 8L04, 8L05, 8I07
    Where it was sold
    Nationwide
    Amount recalled
    2214 units
    Status
    Ended Apr 26, 2019 (FDA lists it as terminated)
    FDA recall number
    F-0801-2019
  6. ENDEDClass II ยท ModerateRecalled Dec 19, 2018

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

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

    CHICAGO BAR COMPANY LLC RXBAR ยท Chicago, IL

    Where it was sold: 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 ...

    UPC 057777004212UPC 057777004281UPC 058030008442UPC 057777004915
    Show details
    Product, as FDA describes it
    Coconut Chocolate RXBARs , 1.83 oz., single bar, , 12-count carton, 5-count carton, 4-count carton
    Reason, in FDA's words
    Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
    Codes on the package
    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
    Where it was sold
    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
    Amount recalled
    75,695,266 Individually wrapped bars
    Status
    Ended Sep 29, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0878-2019
  7. ENDEDClass II ยท ModerateRecalled Dec 19, 2018

    Chocolate Sea Salt RXBARs , 1.83 oz., single bar, , 12-count carton, 10-count carton, , 5-count cart...

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

    CHICAGO BAR COMPANY LLC RXBAR ยท Chicago, IL

    Where it was sold: 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 ...

    UPC 057777004236UPC 057777004304UPC 059162007204UPC 058030008411and 1 more in the details
    Show details
    Product, as FDA describes it
    Chocolate Sea Salt RXBARs , 1.83 oz., single bar, , 12-count carton, 10-count carton, , 5-count carton, 4-count carton
    Reason, in FDA's words
    Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
    Codes on the package
    single bar, UPC 57777 00423, 12-count carton, UPC 57777 00430, 10- count carton, UPC 59162 00720, 5-count carton, UPC 58030 00841, 4-count carton, UPC 57777 00448 Best By Dates between 3/4/2019 9/11/2019 and on 10/11/2019 only
    Where it was sold
    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
    All UPCs
    057777004236, 057777004304, 059162007204, 058030008411, 057777004489
    Amount recalled
    75,695,266 Individually wrapped bars
    Status
    Ended Sep 29, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0879-2019
  8. ENDEDClass II ยท ModerateRecalled Dec 19, 2018

    RXBAR: Apple Cinnamon,1.83oz bars, single bar, 12-count carton,

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

    CHICAGO BAR COMPANY LLC RXBAR ยท Chicago, IL

    Where it was sold: 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 ...

    UPC 057777004175UPC 057777004243
    Show details
    Product, as FDA describes it
    RXBAR: Apple Cinnamon,1.83oz bars, single bar, 12-count carton,
    Reason, in FDA's words
    Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
    Codes on the package
    Apple Cinnamon, single bar, UPC 57777 00417, 12-count carton, UPC 57777 00424, Best By Dates between 4/16/2019 - 5/12/2019 and 7/10/2019 - 7/11/2019
    Where it was sold
    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
    Amount recalled
    75,695,266 Individually wrapped bars
    Status
    Ended Sep 29, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0880-2019
  9. ENDEDClass II ยท ModerateRecalled Dec 19, 2018

    RXBAR:Blueberry, 1.83oz bars, single bar, 12-count carton, , 10-count carton, , 5-count carton, , 4...

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

    CHICAGO BAR COMPANY LLC RXBAR ยท Chicago, IL

    Where it was sold: 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 ...

    UPC 057777004199UPC 057777004267UPC 058030008404UPC 058030008435and 1 more in the details
    Show details
    Product, as FDA describes it
    RXBAR:Blueberry, 1.83oz bars, single bar, 12-count carton, , 10-count carton, , 5-count carton, , 4-count carton
    Reason, in FDA's words
    Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
    Codes on the package
    Blueberry, single bar, UPC 57777 00419, 12-count carton, UPC 57777 00426 , 10-count carton, UPC 58030 00840, 5-count carton, UPC 58030 00843, 4-count carton, UPC 5777700447, Best By Dates between 3/21/2019 5/21/2019 and 7/7/2019 9/29/2019
    Where it was sold
    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
    All UPCs
    057777004199, 057777004267, 058030008404, 058030008435, 057777004472
    Amount recalled
    75,695,266 Individually wrapped bars
    Status
    Ended Sep 29, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0881-2019
  10. ENDEDClass II ยท ModerateRecalled Dec 19, 2018

    RXBAR: Chocolate Chip, 1.83oz bars, single bar,, 12-count carton, , 5-count carton,, 4-count carton

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

    CHICAGO BAR COMPANY LLC RXBAR ยท Chicago, IL

    Where it was sold: 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 ...

    UPC 057777004694UPC 057777004724UPC 058030008459UPC 057777004922
    Show details
    Product, as FDA describes it
    RXBAR: Chocolate Chip, 1.83oz bars, single bar,, 12-count carton, , 5-count carton,, 4-count carton
    Reason, in FDA's words
    Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
    Codes on the package
    Chocolate Chip, 1.83oz bars, single bar, UPC 57777 00469, 12-count carton, UPC 57777 00472, 5-count carton, UPC 58030 00845, 4-count carton, UPC 57777 00492, Best by Dates between 3/24/2019 5/14/2019, 7/11/2019 9/8/2019 and 9/30/2019 10/1/2019
    Where it was sold
    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
    Amount recalled
    75,695,266 Individually wrapped bars
    Status
    Ended Sep 29, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0882-2019
  11. ENDEDClass II ยท ModerateRecalled Dec 19, 2018

    RXBAR: Chocolate Hazelnut, 1.83oz bars single bar, 12-count carton, 4-count carton

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

    CHICAGO BAR COMPANY LLC RXBAR ยท Chicago, IL

    Where it was sold: 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 ...

    UPC 059162007099UPC 059162007105UPC 059162007174
    Show details
    Product, as FDA describes it
    RXBAR: Chocolate Hazelnut, 1.83oz bars single bar, 12-count carton, 4-count carton
    Reason, in FDA's words
    Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
    Codes on the package
    Chocolate Hazelnut, single bar, UPC 59162 00709, 12-count carton, UPC 59162 00710, 4-count carton, UPC 59162 00717, Best By Dates between 2/17/2019 10/18/2019
    Where it was sold
    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
    Amount recalled
    75,695,266 Individually wrapped bars
    Status
    Ended Sep 29, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0883-2019
  12. ENDEDClass II ยท ModerateRecalled Dec 19, 2018

    RXBAR: Coffee Chocolate, 1.83oz bars, single bar, , 12-count carton

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

    CHICAGO BAR COMPANY LLC RXBAR ยท Chicago, IL

    Where it was sold: 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 ...

    UPC 057777004229UPC 057777004298
    Show details
    Product, as FDA describes it
    RXBAR: Coffee Chocolate, 1.83oz bars, single bar, , 12-count carton
    Reason, in FDA's words
    Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
    Codes on the package
    Coffee Chocolate, single bar, UPC 57777 00422, 12-count carton, UPC 57777 00429, Best By Dates between 4/13/2019 8/15/2019
    Where it was sold
    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
    Amount recalled
    75,695,266 Individually wrapped bars
    Status
    Ended Sep 29, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0884-2019
  13. ENDEDClass II ยท ModerateRecalled Dec 19, 2018

    RXBAR: Mango Pineapple,1.83oz bars, single bar, 12-count carton, 4- count carton

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

    CHICAGO BAR COMPANY LLC RXBAR ยท Chicago, IL

    Where it was sold: 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 ...

    UPC 057777004946UPC 057777004953UPC 059162007181
    Show details
    Product, as FDA describes it
    RXBAR: Mango Pineapple,1.83oz bars, single bar, 12-count carton, 4- count carton
    Reason, in FDA's words
    Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
    Codes on the package
    Mango Pineapple, single bar, UPC 57777 00494, 12-count carton, UPC 57777 00495, 4-count carton, UPC 59162 00718, Best By Dates between 2/16/2019 10/19/2019
    Where it was sold
    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
    Amount recalled
    75,695,266 Individually wrapped bars
    Status
    Ended Sep 29, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0885-2019
  14. ENDEDClass II ยท ModerateRecalled Dec 19, 2018

    RXBAR: Maple Sea Salt, 1.83 oz bars, single bar, 2-count carton, 4-count carton

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

    CHICAGO BAR COMPANY LLC RXBAR ยท Chicago, IL

    Where it was sold: 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 ...

    UPC 057777004410UPC 057777004403UPC 057777004540
    Show details
    Product, as FDA describes it
    RXBAR: Maple Sea Salt, 1.83 oz bars, single bar, 2-count carton, 4-count carton
    Reason, in FDA's words
    Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
    Codes on the package
    Maple Sea Salt, single bar, UPC 57777 00441, 12-count carton, UPC 57777 00440, 4-count carton, UPC 57777 00454 Best By Dates between 3/2/2019 5/23/2019, 7/18/2019 7/19/2019 and 9/9/2019 9/10/2019
    Where it was sold
    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
    Amount recalled
    75,695,266 Individually wrapped bars
    Status
    Ended Sep 29, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0886-2019
  15. ENDEDClass II ยท ModerateRecalled Dec 19, 2018

    RXBAR: Mint Chocolate, 1.83 oz. bars, single bar, 12-count carton, 4-count carton

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

    CHICAGO BAR COMPANY LLC RXBAR ยท Chicago, IL

    Where it was sold: 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 ...

    UPC 057777004335UPC 057777004342UPC 057777004496
    Show details
    Product, as FDA describes it
    RXBAR: Mint Chocolate, 1.83 oz. bars, single bar, 12-count carton, 4-count carton
    Reason, in FDA's words
    Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
    Codes on the package
    Mint Chocolate, single bar, UPC 57777 00433, 12-count carton, UPC 57777 00434, 4-count carton, UPC 57777 00449 Best By Dates between 3/2/2019 4/18/2019 and 7/26/2019 8/9/2019
    Where it was sold
    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
    Amount recalled
    75,695,266 Individually wrapped bars
    Status
    Ended Sep 29, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0887-2019
  16. ENDEDClass II ยท ModerateRecalled Dec 19, 2018

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

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

    CHICAGO BAR COMPANY LLC RXBAR ยท Chicago, IL

    Where it was sold: 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 ...

    UPC 057777004700UPC 057777004670UPC 059162007006
    Show details
    Product, as FDA describes it
    RXBAR: Mixed Berry, single bar, 12-count carton, UPC 57777 00470, 4-count carton
    Reason, in FDA's words
    Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
    Codes on the package
    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
    Where it was sold
    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
    Amount recalled
    75,695,266 Individually wrapped bars
    Status
    Ended Sep 29, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0888-2019
  17. ENDEDClass II ยท ModerateRecalled Dec 19, 2018

    RXBAR: KIDS Apple Cinnamon Raisin, 1.16oz bars, single bar, 16-count carton, 5-count carton

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

    CHICAGO BAR COMPANY LLC RXBAR ยท Chicago, IL

    Where it was sold: 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 ...

    UPC 057777004229UPC 057777004298
    Show details
    Product, as FDA describes it
    RXBAR: KIDS Apple Cinnamon Raisin, 1.16oz bars, single bar, 16-count carton, 5-count carton
    Reason, in FDA's words
    Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
    Codes on the package
    Coffee Chocolate, single bar, UPC 57777 00422, 12-count carton, UPC 57777 00429, Best By Dates between 4/13/2019 8/15/2019
    Where it was sold
    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
    Amount recalled
    75,695,266 Individually wrapped bars
    Status
    Ended Sep 29, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0889-2019
  18. ENDEDClass II ยท ModerateRecalled Dec 19, 2018

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

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

    CHICAGO BAR COMPANY LLC RXBAR ยท Chicago, IL

    Where it was sold: 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 ...

    UPC 057777004755UPC 057777004786UPC 057777004519
    Show details
    Product, as FDA describes it
    KIDS Berry Blast, 1.16 oz. bars, single bar, 16-count carton, 5-count carton
    Reason, in FDA's words
    Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
    Codes on the package
    KIDS Berry Blast, single bar, UPC 57777 00475, 16-count carton, UPC 57777 00478, 5-count carton, UPC 57777 00451 Best By Dates between 3/14/2019 4/26/2019 and 6/6/2019 8/5/2019
    Where it was sold
    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
    Amount recalled
    75,695,266 Individually wrapped bars
    Status
    Ended Sep 29, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0890-2019
  19. ENDEDClass II ยท ModerateRecalled Dec 19, 2018

    KIDS Chocolate Chip, 1.16 oz. bars, single bar, 16-count carton, 5-count carton

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

    CHICAGO BAR COMPANY LLC RXBAR ยท Chicago, IL

    Where it was sold: 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 ...

    UPC 057777004762UPC 057777004809UPC 057777004526
    Show details
    Product, as FDA describes it
    KIDS Chocolate Chip, 1.16 oz. bars, single bar, 16-count carton, 5-count carton
    Reason, in FDA's words
    Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
    Codes on the package
    KIDS Chocolate Chip, single bar, UPC 57777 00476, 16-count carton, UPC 57777 00480, 5- count carton, UPC 57777 00452, Best By Dates between 3/15/2019 4/14/2019 and 7/17/2019 9/21/2019
    Where it was sold
    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
    Amount recalled
    75,695,266 Individually wrapped bars
    Status
    Ended Sep 29, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0891-2019
  20. ENDEDClass II ยท ModerateRecalled Dec 19, 2018

    RXBAR: Pumpkin Spice, single bar, 12-count carton, 4-count carton, 1.83 oz bars

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

    CHICAGO BAR COMPANY LLC RXBAR ยท Chicago, IL

    Where it was sold: 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 ...

    UPC 057777004182UPC 057777004250UPC 059162007198
    Show details
    Product, as FDA describes it
    RXBAR: Pumpkin Spice, single bar, 12-count carton, 4-count carton, 1.83 oz bars
    Reason, in FDA's words
    Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
    Codes on the package
    Pumpkin Spice, single bar, UPC 57777 00418, 12-count carton, UPC 57777 00425, 4-count carton, UPC 59162 00719 Best By Dates between 5/9/2019 7/11/2019
    Where it was sold
    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
    Amount recalled
    75,695,266 Individually wrapped bars
    Status
    Ended Sep 29, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0892-2019

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What the classes mean

Class I ยท Most serious. FDA's highest level: products that could cause serious health problems or death.

Class II ยท Moderate. It may cause temporary health problems, or the risk of serious harm is remote.

Class III ยท Low risk. Not likely to cause health problems, but it breaks a labeling or manufacturing rule.

If you have a recalled product

  1. Match the codes on your package to the recall.
  2. If they match, don't eat it.
  3. Return it to the store or throw it away, as the company directs.
  4. If you feel sick, contact your doctor.

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Recall information comes from FDA's enforcement reports through openFDA. FDA publishes new reports weekly; we check every recall's status daily. This page is for information only and is not medical advice. Meat, poultry and egg products are recalled by USDA, not FDA, and are not listed here.