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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

550 recalls · showing 241 to 260

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  1. ENDEDClass II · ModerateRecalled May 8, 2017

    GnuPharma Fit 100% Herbal Supplement 60 Capsules

    1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)

    GnuPharma Corp. · Owasso, OK

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

    Where it was sold: US

    Show details
    Product, as FDA describes it
    GnuPharma Fit 100% Herbal Supplement 60 Capsules
    Reason, in FDA's words
    1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
    Codes on the package
    products manufactured prior to May 8th, 2017.
    Where it was sold
    US
    Amount recalled
    56 bottles
    Status
    Ended Nov 15, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0296-2017
    View in FDA's recall database
  2. ENDEDClass II · ModerateRecalled May 8, 2017

    GnuPharma Relief 100% Herbal Supplement 60 Capsules

    1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)

    GnuPharma Corp. · Owasso, OK

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

    Where it was sold: US

    Show details
    Product, as FDA describes it
    GnuPharma Relief 100% Herbal Supplement 60 Capsules
    Reason, in FDA's words
    1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
    Codes on the package
    products manufactured prior to May 8th, 2017.
    Where it was sold
    US
    Amount recalled
    244 bottles
    Status
    Ended Nov 15, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0297-2017
    View in FDA's recall database
  3. ENDEDClass II · ModerateRecalled May 8, 2017

    GnuPharma Sleep 100% Herbal Supplement 60 Capsules

    1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)

    GnuPharma Corp. · Owasso, OK

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

    Where it was sold: US

    Show details
    Product, as FDA describes it
    GnuPharma Sleep 100% Herbal Supplement 60 Capsules
    Reason, in FDA's words
    1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
    Codes on the package
    products manufactured prior to May 8th, 2017.
    Where it was sold
    US
    Amount recalled
    1 bottle
    Status
    Ended Nov 15, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0298-2017
    View in FDA's recall database
  4. ENDEDClass II · ModerateRecalled May 8, 2017

    GnuPharma Stress 100% Herbal Supplement 60 Capsules

    1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)

    GnuPharma Corp. · Owasso, OK

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

    Where it was sold: US

    Show details
    Product, as FDA describes it
    GnuPharma Stress 100% Herbal Supplement 60 Capsules
    Reason, in FDA's words
    1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
    Codes on the package
    products manufactured prior to May 8th, 2017.
    Where it was sold
    US
    Amount recalled
    131 bottles
    Status
    Ended Nov 15, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0299-2017
    View in FDA's recall database
  5. ENDEDClass II · ModerateRecalled May 8, 2017

    GnuPharma Foundation 100% Herbal Supplement 60 Capsules

    1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)

    GnuPharma Corp. · Owasso, OK

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

    Where it was sold: US

    Show details
    Product, as FDA describes it
    GnuPharma Foundation 100% Herbal Supplement 60 Capsules
    Reason, in FDA's words
    1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
    Codes on the package
    products manufactured prior to May 8th, 2017.
    Where it was sold
    US
    Amount recalled
    9 bottles
    Status
    Ended Nov 15, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0300-2017
    View in FDA's recall database
  6. ENDEDClass II · ModerateRecalled May 8, 2017

    GnuPharma ECS Herbal Tea Relief SAMPLE ONLY

    1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)

    GnuPharma Corp. · Owasso, OK

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

    Where it was sold: US

    Show details
    Product, as FDA describes it
    GnuPharma ECS Herbal Tea Relief SAMPLE ONLY
    Reason, in FDA's words
    1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
    Codes on the package
    products manufactured prior to May 8th, 2017.
    Where it was sold
    US
    Amount recalled
    1 unit (4 tablespoons)
    Status
    Ended Nov 15, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0301-2017
    View in FDA's recall database
  7. ENDEDClass I · Most seriousRecalled May 4, 2017

    Robin Hood ENRICHED & PRE-SIFTED ALL PURPOSE flour ORIGINAL, UPC 0 59000 01632 0, 1 kg

    Possible E. coli O121 contamination

    Bedessee Imports, Inc · Brooklyn, NY

    Where it was sold: FL through one store

    UPC 059000016320
    Show details
    Product, as FDA describes it
    Robin Hood ENRICHED & PRE-SIFTED ALL PURPOSE flour ORIGINAL, UPC 0 59000 01632 0, 1 kg
    Reason, in FDA's words
    Possible E. coli O121 contamination
    Codes on the package
    Lot codes containing BB/MA 6 288 548, 6 289 548, 6 290 548, 6 291 548 Best Before April 2018
    Where it was sold
    FL through one store
    Amount recalled
    4 bales x 12 units x 1 kg
    Status
    Ended Jun 27, 2019 (FDA lists it as terminated)
    FDA recall number
    F-2276-2017
    View in FDA's recall database
  8. ENDEDClass II · ModerateRecalled Apr 26, 2017

    ARTISAN-STYLE PIZZA DOUGH BALL distributed under the following sizes and Product Codes: (a) 12 OZ AR...

    The product was made with flour supplied by Ardent Mills who issued a recall on flour products due to possible E. coli 0121 contamination.

    Rich Products Corp · Buffalo, NY

    Where it was sold: AR, AZ, CA, CO, CT, FL, GA, IA, IA, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI

    UPC 049800112681UPC 049800112698UPC 049800112704
    Show details
    Product, as FDA describes it
    ARTISAN-STYLE PIZZA DOUGH BALL distributed under the following sizes and Product Codes: (a) 12 OZ ARTISAN-STYLE PIZZA DOUGH BALL, RICH'S label, Product Code 11268, UPC 0 00 49800 11268 1, NET CASE WT: 12.2 KG (27 LB), UNIT NET WT: 340 G (12G), COUNT: 36; (b) 18 OZ ARTISAN-STYLE PIZZA DOUGH BALL, Product Code 11269, UPC 0 00 49800 11269 8, NET CASE WT: 12.2 KG (27 LB), UNIT NET WT: 510 (G) (1 LB 2 OZ), COUNT: 24; and (c) 22 OZ ARTISAN-STYLE PIZZA DOUGH BALL, Product Code 11270, UPC 0 00 49800 11270 4 , NET CASE WT: 13 KG (28 LB 14 OZ), UNIT NET WT: 623 G (22 OZ) (1 LB 6 OZ), COUNT: 21 --- PROCESSED IN CANADA, DIST. BY RICH PRODUCTS CORPORATION, BUFFALO, N.Y. 14213 U.S.A.
    Reason, in FDA's words
    The product was made with flour supplied by Ardent Mills who issued a recall on flour products due to possible E. coli 0121 contamination.
    Codes on the package
    (a) Product Code 11268: Lot 77006354, Use By 18/Apr/17; Lot 77007003, Use by 03/May/17; Lot 77007004, Use by 04/May/17; Lot 77007009, Use by 09/May/17; Lot 77007016, Use by 16/May/17; Lot 77007023, Use by 23/May/17; Lot 77007030, Use by 30/May/17; Lot 77007031, Use by 30/May/17; Lot 77007044, Use by 13/Jun/17; Lot 77007058, Use by 27/Jun/17; - (b) Product Code 11269: Lot 77007023, Use by 22/Jul/17; Lot 77007044, Use by 12/Aug/17; Lot 77007058, Use by 26/Aug/17; Lot 77007072, Use by 09/Sep/17; Lot 77007079, Use by 16/Sep/17; - (c) Product Code 11270: Lot 77006354, Use by 17/Jun/17; Lot 77007009, Use by 08/Jul/17; Lot 77007023, Use by 22/Jul/17; Lot 77007058, Use by 26/Aug/17.
    Where it was sold
    AR, AZ, CA, CO, CT, FL, GA, IA, IA, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI
    Amount recalled
    13,043 cases US (total for all products)
    Status
    Ended Jan 14, 2021 (FDA lists it as terminated)
    FDA recall number
    F-2242-2017
    View in FDA's recall database
  9. ENDEDClass II · ModerateRecalled Apr 26, 2017

    7 OZ PIZZA DOUGH BALL, PRODUCT CODE 11267, UPC 0 00 49800 1267 4, NET CASE WT 12.9 KG (28 LB 7 OZ), ...

    The product was made with flour supplied by Ardent Mills who issued a recall on flour products due to possible E. coli 0121 contamination.

    Rich Products Corp · Buffalo, NY

    Where it was sold: AR, AZ, CA, CO, CT, FL, GA, IA, IA, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI

    Show details
    Product, as FDA describes it
    7 OZ PIZZA DOUGH BALL, PRODUCT CODE 11267, UPC 0 00 49800 1267 4, NET CASE WT 12.9 KG (28 LB 7 OZ), UNIT NET WT: 198 G (7 OZ), COUNT: 65 --- PROCESSED IN CANADA, DIST. BY RICH PRODUCTS CORPORATION, BUFFALO, N.Y. 14213 U.S.A.
    Reason, in FDA's words
    The product was made with flour supplied by Ardent Mills who issued a recall on flour products due to possible E. coli 0121 contamination.
    Codes on the package
    Lot 77006354, Use By 18/Apr/17; Lot 77006355, Use By 19/Apr/17; Lot 77007009, Use By 9/May/17; Lot 77007010, Use By 10/May/17; Lot 77007016, Use by 16/May/17; Lot 77007023, Use by 23/May/17; Lot 77007024, Use by 24/May/17; Lot 77007031, Use by 31/May/17; Lot 77007045, Use by 14/Jun/17; 77007058, Use by 27/Jun/17; Lot 77007059, Use by 28/Jun/17; Lot 77007072, Use by 11/Jun/17; Lot 77007073, Use by 12/Jun/17.
    Where it was sold
    AR, AZ, CA, CO, CT, FL, GA, IA, IA, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI
    Amount recalled
    13,043 cases US (total for all products)
    Status
    Ended Jan 14, 2021 (FDA lists it as terminated)
    FDA recall number
    F-2243-2017
    View in FDA's recall database
  10. ENDEDClass II · ModerateRecalled Apr 26, 2017

    ARTISAN CRUST PIZZA DOUGH 24/18, PRODUCT CODE 11413, UPC 1 00 49800 11413 2, NET CASE WT: 27 LB (12....

    The product was made with flour supplied by Ardent Mills who issued a recall on flour products due to possible E. coli 0121 contamination.

    Rich Products Corp · Buffalo, NY

    Where it was sold: AR, AZ, CA, CO, CT, FL, GA, IA, IA, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI

    UPC 10049800114132
    Show details
    Product, as FDA describes it
    ARTISAN CRUST PIZZA DOUGH 24/18, PRODUCT CODE 11413, UPC 1 00 49800 11413 2, NET CASE WT: 27 LB (12.2 KG), UNIT NET WT: 18 OZ (1 LB 2 OZ) (510G), COUNT: 24 --- PROCESSED IN CANADA DIST. BY RICH PRODUCTS CORPORATION, BUFFALO, N.Y. 14213 U.S.A.
    Reason, in FDA's words
    The product was made with flour supplied by Ardent Mills who issued a recall on flour products due to possible E. coli 0121 contamination.
    Codes on the package
    Julian Date 77007072, Use by 08/Nov/17
    Where it was sold
    AR, AZ, CA, CO, CT, FL, GA, IA, IA, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI
    Amount recalled
    13,043 cases US (total for all products)
    Status
    Ended Jan 14, 2021 (FDA lists it as terminated)
    FDA recall number
    F-2244-2017
    View in FDA's recall database
  11. ENDEDClass I · Most seriousRecalled Mar 20, 2017

    20/20 LifeStyles Yogurt Peanut Crunch Bar. Bar UPC 7 8571 00052. Each bar has net weight 2 oz....

    Product is recalled due to a potential contamination with E. coli O157:H7.

    Pro Sports Club · Bellevue, WA

    Where it was sold: Distributed in WA and sold to internet customers through www.2020lifestyles.com.

    UPC 078571000521UPC 078571000538UPC 078571000545
    Show details
    Product, as FDA describes it
    20/20 LifeStyles Yogurt Peanut Crunch Bar. Bar UPC 7 8571 00052. Each bar has net weight 2 oz. Box UPC 7 8571 00053. Each box has 12/2 oz. bars. Case UPC 78571 00054. Each case has 12 boxes and it is for shipment only and not for resale.
    Reason, in FDA's words
    Product is recalled due to a potential contamination with E. coli O157:H7.
    Codes on the package
    B.B. 22JUL17 2046 This lot means Best By July 22, 2017 and Julian date 2046 represents the production date.
    Where it was sold
    Distributed in WA and sold to internet customers through www.2020lifestyles.com.
    Amount recalled
    36,957 bars (2 oz. per bar).
    Status
    Ended Jul 11, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1913-2017
    View in FDA's recall database
  12. ACTIVEClass I · Most seriousRecalled Mar 9, 2017

    Pan Pita with soynut butter spread on top, 4" pita. Manufactured by Greater Miami Caterers 4001 NW 3...

    Possible contamination with E. coli O157

    Greater Miami Caterers, Inc. · Miami, FL

    Where it was sold: Product is distributed throughout Florida to child care programs and after school programs for children.

    Show details
    Product, as FDA describes it
    Pan Pita with soynut butter spread on top, 4" pita. Manufactured by Greater Miami Caterers 4001 NW 31 Ave.,
    Reason, in FDA's words
    Possible contamination with E. coli O157
    Codes on the package
    Product Code 8491. No expiration date
    Where it was sold
    Product is distributed throughout Florida to child care programs and after school programs for children.
    Amount recalled
    Approx. 43,776 portion cups, 16,000 sandwiches, 1,120 lb in various sized repackaged containers
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    F-1949-2017
    View in FDA's recall database
  13. ACTIVEClass I · Most seriousRecalled Mar 9, 2017

    Half Wheat sandwich with soynut butter spread and jelly, served on tray. Manufactured by Greater Mi...

    Possible contamination with E. coli O157

    Greater Miami Caterers, Inc. · Miami, FL

    Where it was sold: Product is distributed throughout Florida to child care programs and after school programs for children.

    Show details
    Product, as FDA describes it
    Half Wheat sandwich with soynut butter spread and jelly, served on tray. Manufactured by Greater Miami Caterers 4001 NW 31 Ave.,
    Reason, in FDA's words
    Possible contamination with E. coli O157
    Codes on the package
    Product Code 8464. No expiration date
    Where it was sold
    Product is distributed throughout Florida to child care programs and after school programs for children.
    Amount recalled
    Approx. 43,776 portion cups, 16,000 sandwiches, 1,120 lb in various sized repackaged containers
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    F-1950-2017
    View in FDA's recall database
  14. ACTIVEClass I · Most seriousRecalled Mar 9, 2017

    Whole Wheat sandwich with soynut butter spread and jelly, served on tray. Manufactured by Greater M...

    Possible contamination with E. coli O157

    Greater Miami Caterers, Inc. · Miami, FL

    Where it was sold: Product is distributed throughout Florida to child care programs and after school programs for children.

    Show details
    Product, as FDA describes it
    Whole Wheat sandwich with soynut butter spread and jelly, served on tray. Manufactured by Greater Miami Caterers 4001 NW 31 Ave.,
    Reason, in FDA's words
    Possible contamination with E. coli O157
    Codes on the package
    Product Code 8465. No expiration date
    Where it was sold
    Product is distributed throughout Florida to child care programs and after school programs for children.
    Amount recalled
    Approx. 43,776 portion cups, 16,000 sandwiches, 1,120 lb in various sized repackaged containers
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    F-1951-2017
    View in FDA's recall database
  15. ACTIVEClass I · Most seriousRecalled Mar 9, 2017

    Portion cup of soynut butter served with other food items such as milk, yogurt, raisins, and gold fi...

    Possible contamination with E. coli O157

    Greater Miami Caterers, Inc. · Miami, FL

    Where it was sold: Product is distributed throughout Florida to child care programs and after school programs for children.

    Show details
    Product, as FDA describes it
    Portion cup of soynut butter served with other food items such as milk, yogurt, raisins, and gold fish crackers, labeled and served on tray. Manufactured by Greater Miami Caterers 4001 NW 31 Ave.,
    Reason, in FDA's words
    Possible contamination with E. coli O157
    Codes on the package
    Product Code 8743. No expiration date
    Where it was sold
    Product is distributed throughout Florida to child care programs and after school programs for children.
    Amount recalled
    Approx. 43,776 portion cups, 16,000 sandwiches, 1,120 lb in various sized repackaged containers
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    F-1952-2017
    View in FDA's recall database
  16. ACTIVEClass I · Most seriousRecalled Mar 9, 2017

    Soynut Butter repackaged into smaller containers and labeled. Container amounts vary according to h...

    Possible contamination with E. coli O157

    Greater Miami Caterers, Inc. · Miami, FL

    Where it was sold: Product is distributed throughout Florida to child care programs and after school programs for children.

    Show details
    Product, as FDA describes it
    Soynut Butter repackaged into smaller containers and labeled. Container amounts vary according to how servings are needed per order. Each serving size is 0.56 oz.. Manufactured by Greater Miami Caterers 4001 NW 31 Ave.,
    Reason, in FDA's words
    Possible contamination with E. coli O157
    Codes on the package
    Product Code 8458. No expiration date
    Where it was sold
    Product is distributed throughout Florida to child care programs and after school programs for children.
    Amount recalled
    Approx. 43,776 portion cups, 16,000 sandwiches, 1,120 lb in various sized repackaged containers
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    F-1953-2017
    View in FDA's recall database
  17. ENDEDClass I · Most seriousRecalled Mar 3, 2017

    I.M. Healthy, Creamy SoyNut Butter; Peanut Free; The SoyNut butter Company, Glenview, IL 60025

    Potential contamination of product with E. coli O157.

    The SoyNut Butter Company · Glenview, IL

    Where it was sold: Nationwide

    Show details
    Product, as FDA describes it
    I.M. Healthy, Creamy SoyNut Butter; Peanut Free; The SoyNut butter Company, Glenview, IL 60025
    Reason, in FDA's words
    Potential contamination of product with E. coli O157.
    Codes on the package
    All lots
    Where it was sold
    Nationwide
    Amount recalled
    642,060 15OZ jars; 32,034 4LB tubs; 436,608 individual cups; 1,275 45LB pails
    Status
    Ended Dec 30, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1901-2017
    View in FDA's recall database
  18. ENDEDClass I · Most seriousRecalled Mar 3, 2017

    I.M. Healthy, Chunky SoyNut Butter; Peanut Free; The SoyNut butter Company, Glenview, IL 60025

    Potential contamination of product with E. coli O157.

    The SoyNut Butter Company · Glenview, IL

    Where it was sold: Nationwide

    Show details
    Product, as FDA describes it
    I.M. Healthy, Chunky SoyNut Butter; Peanut Free; The SoyNut butter Company, Glenview, IL 60025
    Reason, in FDA's words
    Potential contamination of product with E. coli O157.
    Codes on the package
    All lots
    Where it was sold
    Nationwide
    Amount recalled
    43,452 15OZ jars
    Status
    Ended Dec 30, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1902-2017
    View in FDA's recall database
  19. ENDEDClass I · Most seriousRecalled Mar 3, 2017

    I.M. Healthy, Unsweetened SoyNut Butter; Peanut Free; The SoyNut butter Company, Glenview, IL 60025

    Potential contamination of product with E. coli O157.

    The SoyNut Butter Company · Glenview, IL

    Where it was sold: Nationwide

    Show details
    Product, as FDA describes it
    I.M. Healthy, Unsweetened SoyNut Butter; Peanut Free; The SoyNut butter Company, Glenview, IL 60025
    Reason, in FDA's words
    Potential contamination of product with E. coli O157.
    Codes on the package
    All lots
    Where it was sold
    Nationwide
    Amount recalled
    163,260 15oz jars
    Status
    Ended Dec 30, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1903-2017
    View in FDA's recall database
  20. ENDEDClass I · Most seriousRecalled Mar 3, 2017

    I.M. Healthy, Honey Creamy SoyNut Butter; Peanut Free; The SoyNut butter Company, Glenview, IL 60025

    Potential contamination of product with E. coli O157.

    The SoyNut Butter Company · Glenview, IL

    Where it was sold: Nationwide

    Show details
    Product, as FDA describes it
    I.M. Healthy, Honey Creamy SoyNut Butter; Peanut Free; The SoyNut butter Company, Glenview, IL 60025
    Reason, in FDA's words
    Potential contamination of product with E. coli O157.
    Codes on the package
    All lots
    Where it was sold
    Nationwide
    Amount recalled
    88,596 15oz jars
    Status
    Ended Dec 30, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1904-2017
    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.