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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 · Source: U.S. Food and Drug Administration

1,888 ended recalls · showing 1,441 to 1,460

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  1. ENDEDClass II · ModerateRecalled Jan 13, 2016

    Filled Long Johns 9999954006, 540062, 28 per bulk tote.

    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as...

    Kwik Trip Bakery · La Crosse, WI

    Where it was sold: WI, MN, IA

    Show details
    Product, as FDA describes it
    Filled Long Johns 9999954006, 540062, 28 per bulk tote.
    Reason, in FDA's words
    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as an ingredient.
    Codes on the package
    All lots manufactured prior to but not including 01/13/2016.
    Where it was sold
    WI, MN, IA
    Amount recalled
    approx. 288755.44 product counts for all products
    Status
    Ended Jul 18, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0587-2016
    View in FDA's recall database
  2. ENDEDClass II · ModerateRecalled Jan 13, 2016

    Jelly Bismark 9999954008, 540088, 24 per bulk tote.

    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as...

    Kwik Trip Bakery · La Crosse, WI

    Where it was sold: WI, MN, IA

    Show details
    Product, as FDA describes it
    Jelly Bismark 9999954008, 540088, 24 per bulk tote.
    Reason, in FDA's words
    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as an ingredient.
    Codes on the package
    All lots manufactured prior to but not including 01/13/2016.
    Where it was sold
    WI, MN, IA
    Amount recalled
    approx. 288755.44 product counts for all products
    Status
    Ended Jul 18, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0588-2016
    View in FDA's recall database
  3. ENDEDClass II · ModerateRecalled Jan 13, 2016

    Custard Bismark 9999954007, 540070, 24 per bulk tote.

    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as...

    Kwik Trip Bakery · La Crosse, WI

    Where it was sold: WI, MN, IA

    Show details
    Product, as FDA describes it
    Custard Bismark 9999954007, 540070, 24 per bulk tote.
    Reason, in FDA's words
    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as an ingredient.
    Codes on the package
    All lots manufactured prior to but not including 01/13/2016.
    Where it was sold
    WI, MN, IA
    Amount recalled
    approx. 288755.44 product counts for all products
    Status
    Ended Jul 18, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0589-2016
    View in FDA's recall database
  4. ENDEDClass II · ModerateRecalled Jan 13, 2016

    Triple Choc Bismark 9999954048, 540484, 24 per bulk tote.

    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as...

    Kwik Trip Bakery · La Crosse, WI

    Where it was sold: WI, MN, IA

    Show details
    Product, as FDA describes it
    Triple Choc Bismark 9999954048, 540484, 24 per bulk tote.
    Reason, in FDA's words
    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as an ingredient.
    Codes on the package
    All lots manufactured prior to but not including 01/13/2016.
    Where it was sold
    WI, MN, IA
    Amount recalled
    approx. 288755.44 product counts for all products
    Status
    Ended Jul 18, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0590-2016
    View in FDA's recall database
  5. ENDEDClass II · ModerateRecalled Jan 13, 2016

    Cinnamon Cinnsations, 4 count Net WT 19 oz (540g), 3977953052, 530530.

    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as...

    Kwik Trip Bakery · La Crosse, WI

    Where it was sold: WI, MN, IA

    Show details
    Product, as FDA describes it
    Cinnamon Cinnsations, 4 count Net WT 19 oz (540g), 3977953052, 530530.
    Reason, in FDA's words
    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as an ingredient.
    Codes on the package
    All lots manufactured prior to but not including 01/13/2016.
    Where it was sold
    WI, MN, IA
    Amount recalled
    approx. 288755.44 product counts for all products
    Status
    Ended Jul 18, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0591-2016
    View in FDA's recall database
  6. ENDEDClass II · ModerateRecalled Jan 13, 2016

    Persian, 9999954011 540112, 24 per bulk tote, frozen.

    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as...

    Kwik Trip Bakery · La Crosse, WI

    Where it was sold: WI, MN, IA

    Show details
    Product, as FDA describes it
    Persian, 9999954011 540112, 24 per bulk tote, frozen.
    Reason, in FDA's words
    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as an ingredient.
    Codes on the package
    All lots manufactured prior to but not including 01/13/2016.
    Where it was sold
    WI, MN, IA
    Amount recalled
    approx. 288755.44 product counts for all products
    Status
    Ended Jul 18, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0592-2016
    View in FDA's recall database
  7. ENDEDClass II · ModerateRecalled Jan 13, 2016

    KBS Bagel Cinnamon Crunch Bagel, 9999953939, 539160, 24 per bulk tote.

    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as...

    Kwik Trip Bakery · La Crosse, WI

    Where it was sold: WI, MN, IA

    Show details
    Product, as FDA describes it
    KBS Bagel Cinnamon Crunch Bagel, 9999953939, 539160, 24 per bulk tote.
    Reason, in FDA's words
    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as an ingredient.
    Codes on the package
    All lots manufactured prior to but not including 01/13/2016.
    Where it was sold
    WI, MN, IA
    Amount recalled
    approx. 288755.44 product counts for all products
    Status
    Ended Jul 18, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0593-2016
    View in FDA's recall database
  8. ENDEDClass II · ModerateRecalled Jan 13, 2016

    KBS Cinn Raisin Bagel, 9999953937, 539158, 24 per bulk tote.

    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as...

    Kwik Trip Bakery · La Crosse, WI

    Where it was sold: WI, MN, IA

    Show details
    Product, as FDA describes it
    KBS Cinn Raisin Bagel, 9999953937, 539158, 24 per bulk tote.
    Reason, in FDA's words
    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as an ingredient.
    Codes on the package
    All lots manufactured prior to but not including 01/13/2016.
    Where it was sold
    WI, MN, IA
    Amount recalled
    approx. 288755.44 product counts for all products
    Status
    Ended Jul 18, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0594-2016
    View in FDA's recall database
  9. ENDEDClass II · ModerateRecalled Jan 13, 2016

    KBS Plain Bagel, 9999953936, 539157, 24 per bulk tote.

    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as...

    Kwik Trip Bakery · La Crosse, WI

    Where it was sold: WI, MN, IA

    Show details
    Product, as FDA describes it
    KBS Plain Bagel, 9999953936, 539157, 24 per bulk tote.
    Reason, in FDA's words
    Kwik Trip, Inc. is recalling various bakery goods which might be contaminated with pieces of plastic due to using plastic contaminated ice nuggets as an ingredient.
    Codes on the package
    All lots manufactured prior to but not including 01/13/2016.
    Where it was sold
    WI, MN, IA
    Amount recalled
    approx. 288755.44 product counts for all products
    Status
    Ended Jul 18, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0595-2016
    View in FDA's recall database
  10. ENDEDClass II · ModerateRecalled Jan 12, 2016

    Ice Nuggets, 10 lb plastic bag, UPC 3977919140.

    Kwik Trip Inc reported a plastic fan broke which lead to pieces of plastic contaminating the ice.

    Kwik Trip, Inc. · La Crosse, WI

    Where it was sold: WI, IA, MN.

    UPC 039779191404
    Show details
    Product, as FDA describes it
    Ice Nuggets, 10 lb plastic bag, UPC 3977919140.
    Reason, in FDA's words
    Kwik Trip Inc reported a plastic fan broke which lead to pieces of plastic contaminating the ice.
    Codes on the package
    All lots with dates prior to 01/11/16.
    Where it was sold
    WI, IA, MN.
    Amount recalled
    approx. 115339.3 10 lb/bag
    Status
    Ended Aug 25, 2016 (FDA lists it as terminated)
    FDA recall number
    F-1835-2016
    View in FDA's recall database
  11. ENDEDClass II · ModerateRecalled Dec 29, 2015

    CapriSun fruit punch roarin'waters packaged in a blue and white box with pictures of fruit and white...

    Possible presence of glass fragments in CapriSun and Kool-Aid Jammers.

    Kraft Heinz Foods · Northfield, IL

    Sold in the U.S. (states not listed)

    Where it was sold: The firm distributed the product to 132 domestic firms. Please see the attached spreadsheet for a list of all consignees.

    Show details
    Product, as FDA describes it
    CapriSun fruit punch roarin'waters packaged in a blue and white box with pictures of fruit and white lettering.
    Reason, in FDA's words
    Possible presence of glass fragments in CapriSun and Kool-Aid Jammers.
    Codes on the package
    best when used by code date: 08 DEC 2016 GR02CT762 and 09 DEC 2016 GR02CT762
    Where it was sold
    The firm distributed the product to 132 domestic firms. Please see the attached spreadsheet for a list of all consignees.
    Amount recalled
    20, 298 cases, 4 boxes/case, 10 drinks/box
    Status
    Ended Feb 21, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1391-2016
    View in FDA's recall database
  12. ENDEDClass II · ModerateRecalled Dec 29, 2015

    CapriSun tropical punch packaged in a blue and white box with pictures of fruit and white and black ...

    Possible presence of glass fragments in CapriSun and Kool-Aid Jammers.

    Kraft Heinz Foods · Northfield, IL

    Sold in the U.S. (states not listed)

    Where it was sold: The firm distributed the product to 132 domestic firms. Please see the attached spreadsheet for a list of all consignees.

    Show details
    Product, as FDA describes it
    CapriSun tropical punch packaged in a blue and white box with pictures of fruit and white and black lettering.
    Reason, in FDA's words
    Possible presence of glass fragments in CapriSun and Kool-Aid Jammers.
    Codes on the package
    best when used by code date: 09 DEC 2016 GR02CT762
    Where it was sold
    The firm distributed the product to 132 domestic firms. Please see the attached spreadsheet for a list of all consignees.
    Amount recalled
    20, 298 cases, 4 boxes/case, 10 drinks/box.
    Status
    Ended Feb 21, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1392-2016
    View in FDA's recall database
  13. ENDEDClass II · ModerateRecalled Dec 29, 2015

    Kool-Aid Jammers Strawberry Kiwi packaged in a green and red box with white lettering.

    Possible presence of glass fragments in CapriSun and Kool-Aid Jammers.

    Kraft Heinz Foods · Northfield, IL

    Sold in the U.S. (states not listed)

    Where it was sold: The firm distributed the product to 132 domestic firms. Please see the attached spreadsheet for a list of all consignees.

    Show details
    Product, as FDA describes it
    Kool-Aid Jammers Strawberry Kiwi packaged in a green and red box with white lettering.
    Reason, in FDA's words
    Possible presence of glass fragments in CapriSun and Kool-Aid Jammers.
    Codes on the package
    best when used by code date: 09 DEC 2016 GR02CT762
    Where it was sold
    The firm distributed the product to 132 domestic firms. Please see the attached spreadsheet for a list of all consignees.
    Amount recalled
    20, 298 cases, 4 boxes/case, 10 drinks/box.
    Status
    Ended Feb 21, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1393-2016
    View in FDA's recall database
  14. ENDEDClass II · ModerateRecalled Dec 29, 2015

    Kool-Aid Jammers Grape packaged in a purple and red box with white lettering.

    Possible presence of glass fragments in CapriSun and Kool-Aid Jammers.

    Kraft Heinz Foods · Northfield, IL

    Sold in the U.S. (states not listed)

    Where it was sold: The firm distributed the product to 132 domestic firms. Please see the attached spreadsheet for a list of all consignees.

    Show details
    Product, as FDA describes it
    Kool-Aid Jammers Grape packaged in a purple and red box with white lettering.
    Reason, in FDA's words
    Possible presence of glass fragments in CapriSun and Kool-Aid Jammers.
    Codes on the package
    best when used by code date: 10 DEC 2016 GR02CT762
    Where it was sold
    The firm distributed the product to 132 domestic firms. Please see the attached spreadsheet for a list of all consignees.
    Amount recalled
    20, 298 cases, 4 boxes/case, 10 drinks/box.
    Status
    Ended Feb 21, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1394-2016
    View in FDA's recall database
  15. ENDEDClass II · ModerateRecalled Dec 29, 2015

    Kool-Aid Jammers Cherry packaged in a red box with white lettering.

    Possible presence of glass fragments in CapriSun and Kool-Aid Jammers.

    Kraft Heinz Foods · Northfield, IL

    Sold in the U.S. (states not listed)

    Where it was sold: The firm distributed the product to 132 domestic firms. Please see the attached spreadsheet for a list of all consignees.

    Show details
    Product, as FDA describes it
    Kool-Aid Jammers Cherry packaged in a red box with white lettering.
    Reason, in FDA's words
    Possible presence of glass fragments in CapriSun and Kool-Aid Jammers.
    Codes on the package
    best when used by code date: 10 DEC 2016 GR02CT762 and 11 DEC 2016 Gr02CT762
    Where it was sold
    The firm distributed the product to 132 domestic firms. Please see the attached spreadsheet for a list of all consignees.
    Amount recalled
    20, 298 cases, 4 boxes/case, 10 drinks/box.
    Status
    Ended Feb 21, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1395-2016
    View in FDA's recall database
  16. ENDEDClass II · ModerateRecalled Dec 29, 2015

    Kool-Aid Jammers Tropical Punch packaged in a red blue and purple box with white lettering.

    Possible presence of glass fragments in CapriSun and Kool-Aid Jammers.

    Kraft Heinz Foods · Northfield, IL

    Sold in the U.S. (states not listed)

    Where it was sold: The firm distributed the product to 132 domestic firms. Please see the attached spreadsheet for a list of all consignees.

    Show details
    Product, as FDA describes it
    Kool-Aid Jammers Tropical Punch packaged in a red blue and purple box with white lettering.
    Reason, in FDA's words
    Possible presence of glass fragments in CapriSun and Kool-Aid Jammers.
    Codes on the package
    best when used by code date: 11 DEC 2016 Gr02CT762 and 12 DEC 2016 GR02CT762.
    Where it was sold
    The firm distributed the product to 132 domestic firms. Please see the attached spreadsheet for a list of all consignees.
    Amount recalled
    20, 298 cases, 4 boxes/case, 10 drinks/box.
    Status
    Ended Feb 21, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1396-2016
    View in FDA's recall database
  17. ENDEDClass II · ModerateRecalled Dec 23, 2015

    Mandarin Oranges (In Light Syrup), Net Wt. 8oz (227g), Case UPC#: 100-49022-80895-6, Product UPC#: 0...

    MW Polar Foods is recalling Mandarin Oranges due to possible glass in product.

    Milky Way Intl Trading Corp · Norwalk, CA

    Where it was sold: US distribution to Walgreens stores nationwide.

    UPC 10049022808956UPC 049022808959
    Show details
    Product, as FDA describes it
    Mandarin Oranges (In Light Syrup), Net Wt. 8oz (227g), Case UPC#: 100-49022-80895-6, Product UPC#: 0-49022-80895-9
    Reason, in FDA's words
    MW Polar Foods is recalling Mandarin Oranges due to possible glass in product.
    Codes on the package
    Lot numbers: H894K09A 01/11/2017 4200/01039 01/16/2018 4200/01039 02/01/2018
    Where it was sold
    US distribution to Walgreens stores nationwide.
    Amount recalled
    8309 cases
    Status
    Ended Apr 20, 2016 (FDA lists it as terminated)
    FDA recall number
    F-0515-2016
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled Dec 20, 2015

    Signature Breads Frozen Parbaked French Dinner Roll 22245; 120 units - 1.25 OZ NET WT. 9.37 LB (4.25...

    Product may contain metal fragments.

    Signature Breads, Inc. · Chelsea, MA

    Where it was sold: NH, PA, FL

    Show details
    Product, as FDA describes it
    Signature Breads Frozen Parbaked French Dinner Roll 22245; 120 units - 1.25 OZ NET WT. 9.37 LB (4.25 KG), in a cardboard box
    Reason, in FDA's words
    Product may contain metal fragments.
    Codes on the package
    Use by Date: 9/15/2016
    Where it was sold
    NH, PA, FL
    Amount recalled
    1,893 cases Total
    Status
    Ended May 17, 2024 (FDA lists it as terminated)
    FDA recall number
    F-0516-2016
    View in FDA's recall database
  19. ENDEDClass II · ModerateRecalled Dec 20, 2015

    Signature Breads Frozen Parbaked Baguette 22202, 25 UNITS - 8.75 OZ, NET WT. 13.67 LB (6.2 kg), in a...

    Product may contain metal fragments.

    Signature Breads, Inc. · Chelsea, MA

    Where it was sold: NH, PA, FL

    Show details
    Product, as FDA describes it
    Signature Breads Frozen Parbaked Baguette 22202, 25 UNITS - 8.75 OZ, NET WT. 13.67 LB (6.2 kg), in a cardboard box
    Reason, in FDA's words
    Product may contain metal fragments.
    Codes on the package
    Use by Date: 9/14/2016
    Where it was sold
    NH, PA, FL
    Amount recalled
    1,893 cases Total
    Status
    Ended May 17, 2024 (FDA lists it as terminated)
    FDA recall number
    F-0517-2016
    View in FDA's recall database
  20. ENDEDClass II · ModerateRecalled Dec 20, 2015

    Signature Breads Frozen Parbaked French Petit Pain 22203, 144 UNITS - 1.75 OZ, NET WT. 15.75 LB (7.1...

    Product may contain metal fragments.

    Signature Breads, Inc. · Chelsea, MA

    Where it was sold: NH, PA, FL

    Show details
    Product, as FDA describes it
    Signature Breads Frozen Parbaked French Petit Pain 22203, 144 UNITS - 1.75 OZ, NET WT. 15.75 LB (7.14 kg), in a cardboard box
    Reason, in FDA's words
    Product may contain metal fragments.
    Codes on the package
    Use by Date: 9/14/2016
    Where it was sold
    NH, PA, FL
    Amount recalled
    1,893 cases Total
    Status
    Ended May 17, 2024 (FDA lists it as terminated)
    FDA recall number
    F-0518-2016
    View in FDA's recall database

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What the classes mean

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

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

Class III · 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.