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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

1,966 recalls · showing 841 to 860

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  1. ENDEDClass II · ModerateRecalled Jun 23, 2020

    Blanxart 85% Nicaragua Organic Dark Chocolate Bar, packaged in paper packaging with internal foil wr...

    A foreign object found by a consumer in dark chocolate bar.

    Power Selles Imports dba Culinary Collective · Lynnwood, WA

    Where it was sold: Distributed in ID, CA, OR, WA, UT and in CANADA.

    UPC 832924000589
    Show details
    Product, as FDA describes it
    Blanxart 85% Nicaragua Organic Dark Chocolate Bar, packaged in paper packaging with internal foil wrapper. Net weight 4.4 oz (125 g). UPC 8 32924 00058 9. Product's label is read in parts: "***BLANXART 85% NICARAGUA ORGANIC DARK CHOCOLATE***Organic dark chocolate, Cocoa 85% minimum. Ingredients: cocoa, cane sugar, cocoa butter *** BB Chocolate Group, SA c/Tambor del Bruc 13 -17 08970 Sant Joan Desp¿, Spain *** Made in Spain ***Imported by: Culinary Collective Lynnwood, WA ***".
    Reason, in FDA's words
    A foreign object found by a consumer in dark chocolate bar.
    Codes on the package
    Product BX 418, Lot 19112031, date code stamp 3-10 with best by date of 3/27/2021. The code breaks down as follows: Product BX418 (importer code). 49085 (manufacturer code). Lot 19112031 with date code stamp 3-10.
    Where it was sold
    Distributed in ID, CA, OR, WA, UT and in CANADA.
    Amount recalled
    72 cases (16 bars per case)
    Status
    Ended Jul 27, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1016-2020
    View in FDA's recall database
  2. ENDEDClass II · ModerateRecalled Jun 18, 2020

    Coke Zero Sugar 20 oz UPC 049000040869

    Potential that some bottles could contain glass fragments

    Coca Cola · Dallas, TX

    Where it was sold: Corpus Christi and San Antonio, TX Metropolitan areas

    UPC 049000040869
    Show details
    Product, as FDA describes it
    Coke Zero Sugar 20 oz UPC 049000040869
    Reason, in FDA's words
    Potential that some bottles could contain glass fragments
    Codes on the package
    SEP0720LWA
    Where it was sold
    Corpus Christi and San Antonio, TX Metropolitan areas
    Amount recalled
    394 cases
    Status
    Ended Jul 22, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1003-2020
    View in FDA's recall database
  3. ENDEDClass II · ModerateRecalled Jun 18, 2020

    Cherry Coke 20 oz UPC 049000018011

    Potential that some bottles could contain glass fragments

    Coca Cola · Dallas, TX

    Where it was sold: Corpus Christi and San Antonio, TX Metropolitan areas

    UPC 049000018011
    Show details
    Product, as FDA describes it
    Cherry Coke 20 oz UPC 049000018011
    Reason, in FDA's words
    Potential that some bottles could contain glass fragments
    Codes on the package
    SEP0820LWB
    Where it was sold
    Corpus Christi and San Antonio, TX Metropolitan areas
    Amount recalled
    42 cases
    Status
    Ended Jul 22, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1004-2020
    View in FDA's recall database
  4. ENDEDClass II · ModerateRecalled Jun 18, 2020

    Dr Pepper 20 oz UPC 078000082401

    Potential that some bottles could contain glass fragments

    Coca Cola · Dallas, TX

    Where it was sold: Corpus Christi and San Antonio, TX Metropolitan areas

    UPC 078000082401
    Show details
    Product, as FDA describes it
    Dr Pepper 20 oz UPC 078000082401
    Reason, in FDA's words
    Potential that some bottles could contain glass fragments
    Codes on the package
    SEP2920LWB
    Where it was sold
    Corpus Christi and San Antonio, TX Metropolitan areas
    Amount recalled
    24 cases
    Status
    Ended Jul 22, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1005-2020
    View in FDA's recall database
  5. ENDEDClass II · ModerateRecalled Jun 18, 2020

    Dr Pepper Cherry 20 oz UPC 078000098402

    Potential that some bottles could contain glass fragments

    Coca Cola · Dallas, TX

    Where it was sold: Corpus Christi and San Antonio, TX Metropolitan areas

    UPC 078000098402
    Show details
    Product, as FDA describes it
    Dr Pepper Cherry 20 oz UPC 078000098402
    Reason, in FDA's words
    Potential that some bottles could contain glass fragments
    Codes on the package
    SEP2920LWB
    Where it was sold
    Corpus Christi and San Antonio, TX Metropolitan areas
    Amount recalled
    3 cases
    Status
    Ended Jul 22, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1006-2020
    View in FDA's recall database
  6. ENDEDClass II · ModerateRecalled Jun 18, 2020

    Simply Nature Sweet Potato Bites, 12oz retail boxes variety pack, Expiration date 4/9/2022. Lot code...

    Product may contain foreign object.

    Dr. Praeger's Sensible Foods Inc. · Elmwood Park, NJ

    Where it was sold: Product was distributed to ALDI warehouses in multiple states with further distribution to: Alabama, Arkansas, Connecticut, Delaware, Florida, Georgia, Illinois, Indiana, Iowa, Kan...

    Show details
    Product, as FDA describes it
    Simply Nature Sweet Potato Bites, 12oz retail boxes variety pack, Expiration date 4/9/2022. Lot code R20AJ-01A.
    Reason, in FDA's words
    Product may contain foreign object.
    Codes on the package
    Lot code R20AJ-01A
    Where it was sold
    Product was distributed to ALDI warehouses in multiple states with further distribution to: Alabama, Arkansas, Connecticut, Delaware, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Massachusetts, Michigan, Missouri, Mississippi, North Carolina, Nebraska, New Hampshire, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, Tennessee, Virginia, Vermont, Wisconsin, and West Virginia.
    Amount recalled
    51,296 boxes
    Status
    Ended Jun 23, 2022 (FDA lists it as terminated)
    FDA recall number
    F-1011-2020
    View in FDA's recall database
  7. ENDEDClass II · ModerateRecalled May 15, 2020

    Siete Grain Free Cashew Flour Tortillas NET WT 7 OZ (200g) 8 Count UPC 865336000045 packaged in flex...

    Potential to contain foreign material.

    GARZA FOOD VENTURES · Austin, TX

    Where it was sold: Nationwide via distribution centers

    UPC 865336000045
    Show details
    Product, as FDA describes it
    Siete Grain Free Cashew Flour Tortillas NET WT 7 OZ (200g) 8 Count UPC 865336000045 packaged in flexible plastic
    Reason, in FDA's words
    Potential to contain foreign material.
    Codes on the package
    C0220CW, C0320CW, C0420CW, C2120CW, D0620CW, D0720CW
    Where it was sold
    Nationwide via distribution centers
    Amount recalled
    7,260 cases / 38,115 lbs
    Status
    Ended Jun 23, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0959-2020
    View in FDA's recall database
  8. ENDEDClass II · ModerateRecalled May 15, 2020

    Wegmans Tuna Salad, 16 OZ (1 LB) 454 g; UPC: 77890-48147; SELL BY 5/21/20

    Product may contain pieces of metal.

    Wegmans Food Markets, Inc. · Rochester, NY

    Where it was sold: NY, MD, NJ, VA, MA, PA, NC

    UPC 077890481479
    Show details
    Product, as FDA describes it
    Wegmans Tuna Salad, 16 OZ (1 LB) 454 g; UPC: 77890-48147; SELL BY 5/21/20
    Reason, in FDA's words
    Product may contain pieces of metal.
    Codes on the package
    UPC: 77890-48147; SELL BY 5/21/20
    Where it was sold
    NY, MD, NJ, VA, MA, PA, NC
    Amount recalled
    958 units total
    Status
    Ended May 28, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0965-2020
    View in FDA's recall database
  9. ENDEDClass II · ModerateRecalled May 15, 2020

    Wegmans Tuna Salad on Roasted Tomato Pita, 9 oz.; UPC: 2-27390-00000; SELL BY 5/14-5/16

    Product may contain pieces of metal.

    Wegmans Food Markets, Inc. · Rochester, NY

    Where it was sold: NY, MD, NJ, VA, MA, PA, NC

    Show details
    Product, as FDA describes it
    Wegmans Tuna Salad on Roasted Tomato Pita, 9 oz.; UPC: 2-27390-00000; SELL BY 5/14-5/16
    Reason, in FDA's words
    Product may contain pieces of metal.
    Codes on the package
    UPC: 2-27390-00000; SELL BY 5/14-5/16
    Where it was sold
    NY, MD, NJ, VA, MA, PA, NC
    Amount recalled
    958 units total
    Status
    Ended May 28, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0966-2020
    View in FDA's recall database
  10. ENDEDClass II · ModerateRecalled May 15, 2020

    Wegmans Tuna & Provolone Packaged Sub, Medium, 11 oz; UPC: 2-27031-00000; SELL BY 5/14-5/16

    Product may contain pieces of metal.

    Wegmans Food Markets, Inc. · Rochester, NY

    Where it was sold: NY, MD, NJ, VA, MA, PA, NC

    Show details
    Product, as FDA describes it
    Wegmans Tuna & Provolone Packaged Sub, Medium, 11 oz; UPC: 2-27031-00000; SELL BY 5/14-5/16
    Reason, in FDA's words
    Product may contain pieces of metal.
    Codes on the package
    UPC: 2-27031-00000; SELL BY 5/14-5/16
    Where it was sold
    NY, MD, NJ, VA, MA, PA, NC
    Amount recalled
    958 units total
    Status
    Ended May 28, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0967-2020
    View in FDA's recall database
  11. ENDEDClass II · ModerateRecalled May 15, 2020

    Wegmans Packaged Tuna & Provolone Wheat Wrap, 9 oz; UPC: 2-27303-00000; SELL BY 5/14-5/16

    Product may contain pieces of metal.

    Wegmans Food Markets, Inc. · Rochester, NY

    Where it was sold: NY, MD, NJ, VA, MA, PA, NC

    Show details
    Product, as FDA describes it
    Wegmans Packaged Tuna & Provolone Wheat Wrap, 9 oz; UPC: 2-27303-00000; SELL BY 5/14-5/16
    Reason, in FDA's words
    Product may contain pieces of metal.
    Codes on the package
    UPC: 2-27303-00000; SELL BY 5/14-5/16
    Where it was sold
    NY, MD, NJ, VA, MA, PA, NC
    Amount recalled
    958 units total
    Status
    Ended May 28, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0968-2020
    View in FDA's recall database
  12. ENDEDClass II · ModerateRecalled May 14, 2020

    Aminature L-Cysteine HCl Anhydrous 100 mesh 25KG DRUM

    complaint of metal fragments

    Cj Haide (Ningbo) Biotech Co., Ltd · Ningbo, N/A

    Where it was sold: Single distributor in CA

    Show details
    Product, as FDA describes it
    Aminature L-Cysteine HCl Anhydrous 100 mesh 25KG DRUM
    Reason, in FDA's words
    complaint of metal fragments
    Codes on the package
    Lot Numbers: IABF200303
    Where it was sold
    Single distributor in CA
    Amount recalled
    40-25KG DRUMS
    Status
    Ended Sep 3, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1030-2020
    View in FDA's recall database
  13. ENDEDClass II · ModerateRecalled Apr 28, 2020

    Benefiber Healthy Shape Prebiotic Fiber Supplement, 500G UPC 886790018872

    Fiber prebiotic product potentially contaminated with small plastic pieces

    Glaxosmithkline Consumer Healthcare Holdings · Warren, NJ

    Where it was sold: Distributed to the following US states: AR, CA, FL, HI, ID, IL, LA, MA, ME, MI, MN, MO, NC, NE, NJ, NY, OH, OR, PA, RI, SC, TX, VA, WA, and WI

    UPC 886790018872
    Show details
    Product, as FDA describes it
    Benefiber Healthy Shape Prebiotic Fiber Supplement, 500G UPC 886790018872
    Reason, in FDA's words
    Fiber prebiotic product potentially contaminated with small plastic pieces
    Codes on the package
    Lot: MP8B (EXP Sep2021)
    Where it was sold
    Distributed to the following US states: AR, CA, FL, HI, ID, IL, LA, MA, ME, MI, MN, MO, NC, NE, NJ, NY, OH, OR, PA, RI, SC, TX, VA, WA, and WI
    Amount recalled
    29,844 bottles
    Status
    Ended Jun 1, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0950-2020
    View in FDA's recall database
  14. ENDEDClass II · ModerateRecalled Apr 28, 2020

    Benefiber Prebiotic Fiber Supplement, packaged in the following ways 1) Net Wt. 500 g (17.6 oz) bott...

    Fiber prebiotic product potentially contaminated with small plastic pieces

    Glaxosmithkline Consumer Healthcare Holdings · Warren, NJ

    Where it was sold: Distributed to the following US states: AR, CA, FL, HI, ID, IL, LA, MA, ME, MI, MN, MO, NC, NE, NJ, NY, OH, OR, PA, RI, SC, TX, VA, WA, and WI

    UPC 886790218302
    Show details
    Product, as FDA describes it
    Benefiber Prebiotic Fiber Supplement, packaged in the following ways 1) Net Wt. 500 g (17.6 oz) bottle. UPC 886790218302 and 2) Net Wt. 760 g bottle UPC 8886790211907
    Reason, in FDA's words
    Fiber prebiotic product potentially contaminated with small plastic pieces
    Codes on the package
    Lots: YT2Y (EXP Oct 2021), 7D6E (EXP Nov 2021), UV5C (EXP Oct 2021), 648H (EXP Nov 2021)
    Where it was sold
    Distributed to the following US states: AR, CA, FL, HI, ID, IL, LA, MA, ME, MI, MN, MO, NC, NE, NJ, NY, OH, OR, PA, RI, SC, TX, VA, WA, and WI
    Amount recalled
    170,340 bottles
    Status
    Ended Jun 1, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0951-2020
    View in FDA's recall database
  15. ENDEDClass II · ModerateRecalled Feb 28, 2020

    GREAT VALUE¿ Pure Granulated Sugar, 10 lbs. Sold as individual bags on a unitized 1/2 pallet 78 b...

    Possible foreign material: metal pieces

    Domino Foods Inc · West Palm Beach, FL

    Where it was sold: The product was only shipped to one US consignee in PA.

    Show details
    Product, as FDA describes it
    GREAT VALUE¿ Pure Granulated Sugar, 10 lbs. Sold as individual bags on a unitized 1/2 pallet 78 bags to a 1/2 pallet.
    Reason, in FDA's words
    Possible foreign material: metal pieces
    Codes on the package
    Lot Code M0071B7 Best by Date 02/10/2023
    Where it was sold
    The product was only shipped to one US consignee in PA.
    Amount recalled
    4056 bags
    Status
    Ended Jun 12, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0827-2020
    View in FDA's recall database
  16. ENDEDClass II · ModerateRecalled Feb 27, 2020

    Pure Cane Granulated Sugar, Single 10 lb. package, 156 paper bags on 2 1/2 CHEP pallets

    Possible foreign object: metal wire

    Maryland Packaging, LTD. · Elkridge, MD

    Where it was sold: The product was distributed to PA and MD

    Show details
    Product, as FDA describes it
    Pure Cane Granulated Sugar, Single 10 lb. package, 156 paper bags on 2 1/2 CHEP pallets
    Reason, in FDA's words
    Possible foreign object: metal wire
    Codes on the package
    M0071A7 and M0071B7
    Where it was sold
    The product was distributed to PA and MD
    Amount recalled
    4056 bags
    Status
    Ended Jun 11, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0831-2020
    View in FDA's recall database
  17. ENDEDClass II · ModerateRecalled Feb 25, 2020

    Profile Food Ingredients, 10# Choc Dairy Pwd PFI-1010, packaged in 50 lb bags.

    The firm received an ingredient that may have been contaminated with metal fragments and further manufactured and distributed products made with that ...

    International Food Products Corporation · Hazelwood, MO

    Where it was sold: Distributed to customers in CA, IL, and TX

    Show details
    Product, as FDA describes it
    Profile Food Ingredients, 10# Choc Dairy Pwd PFI-1010, packaged in 50 lb bags.
    Reason, in FDA's words
    The firm received an ingredient that may have been contaminated with metal fragments and further manufactured and distributed products made with that ingredient.
    Codes on the package
    T02792-1
    Where it was sold
    Distributed to customers in CA, IL, and TX
    Amount recalled
    21 bags
    Status
    Ended May 4, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0832-2020
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled Feb 25, 2020

    Dairy House Ingredients Systems, Anti-Sticking Starch Blend #9400-50 (501876) packaged in 50 lb bags

    The firm received an ingredient that may have been contaminated with metal fragments and further manufactured and distributed products made with that ...

    International Food Products Corporation · Hazelwood, MO

    Where it was sold: Distributed to customers in CA, IL, and TX

    Show details
    Product, as FDA describes it
    Dairy House Ingredients Systems, Anti-Sticking Starch Blend #9400-50 (501876) packaged in 50 lb bags
    Reason, in FDA's words
    The firm received an ingredient that may have been contaminated with metal fragments and further manufactured and distributed products made with that ingredient.
    Codes on the package
    20028AW2A
    Where it was sold
    Distributed to customers in CA, IL, and TX
    Amount recalled
    95 bags
    Status
    Ended May 4, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0833-2020
    View in FDA's recall database
  19. ENDEDClass II · ModerateRecalled Feb 25, 2020

    Dairy House Ingredients Systems, Chocolate Dairy Powder, 13# 50-91-0089, (501761) 39 packaged in 39 ...

    The firm received an ingredient that may have been contaminated with metal fragments and further manufactured and distributed products made with that ...

    International Food Products Corporation · Hazelwood, MO

    Where it was sold: Distributed to customers in CA, IL, and TX

    Show details
    Product, as FDA describes it
    Dairy House Ingredients Systems, Chocolate Dairy Powder, 13# 50-91-0089, (501761) 39 packaged in 39 lb bags
    Reason, in FDA's words
    The firm received an ingredient that may have been contaminated with metal fragments and further manufactured and distributed products made with that ingredient.
    Codes on the package
    20023AC3G, 20023AC3L, 20023AC3F, 20023AC3I, 20023AC3H
    Where it was sold
    Distributed to customers in CA, IL, and TX
    Amount recalled
    271 bags
    Status
    Ended May 4, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0834-2020
    View in FDA's recall database
  20. ENDEDClass II · ModerateRecalled Feb 24, 2020

    American Bounty brand Icing Mix Vanilla, Item #32595, in 5 lb. metallic pouches, 6 pouches per case.

    Downstream recall from supplier. Possible metal shavings in ingredient.

    Tova Industries Inc · Louisville, KY

    Where it was sold: Products were distributed to the following states: AR, CA, IL, LA, MI, NE, NM, NY, VA, WI, and WY. Product was also distributed to the United Arab Emirates.

    Show details
    Product, as FDA describes it
    American Bounty brand Icing Mix Vanilla, Item #32595, in 5 lb. metallic pouches, 6 pouches per case.
    Reason, in FDA's words
    Downstream recall from supplier. Possible metal shavings in ingredient.
    Codes on the package
    Lot: 20200341B
    Where it was sold
    Products were distributed to the following states: AR, CA, IL, LA, MI, NE, NM, NY, VA, WI, and WY. Product was also distributed to the United Arab Emirates.
    Amount recalled
    104 cases.
    Status
    Ended Apr 12, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0801-2020
    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.