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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

535 ended recalls ยท showing 221 to 240

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  1. ENDEDClass II ยท ModerateRecalled Jul 21, 2017

    The Comfy Cow Double Fold Vanilla Ice Cream 1 pint

    The firm is recalling various brands of ice cream due to E. coli & high Coliform Bacteria counts in various products.

    Koogee-Queen Anne, LLC ยท Louisville, KY

    Where it was sold: Product was shipped to the following states: IN, KY, MO & TN.

    Show details
    Product, as FDA describes it
    The Comfy Cow Double Fold Vanilla Ice Cream 1 pint
    Reason, in FDA's words
    The firm is recalling various brands of ice cream due to E. coli & high Coliform Bacteria counts in various products.
    Codes on the package
    Lot: VAN1CR06292017A1, Best By: 03/31/2018
    Where it was sold
    Product was shipped to the following states: IN, KY, MO & TN.
    Amount recalled
    399 pints
    Status
    Ended Feb 15, 2018 (FDA lists it as terminated)
    FDA recall number
    F-3447-2017
  2. ENDEDClass II ยท ModerateRecalled Jul 21, 2017

    The Comfy Cow Georgia Butter Pecan Ice Cream 1 pint

    The firm is recalling various brands of ice cream due to E. coli & high Coliform Bacteria counts in various products.

    Koogee-Queen Anne, LLC ยท Louisville, KY

    Where it was sold: Product was shipped to the following states: IN, KY, MO & TN.

    Show details
    Product, as FDA describes it
    The Comfy Cow Georgia Butter Pecan Ice Cream 1 pint
    Reason, in FDA's words
    The firm is recalling various brands of ice cream due to E. coli & high Coliform Bacteria counts in various products.
    Codes on the package
    Lot: GBP1CR06122017A1, Best By: 03/14/2018 & Lot: GBP1CR06122017A13-A333, Best By: 03/14/2018
    Where it was sold
    Product was shipped to the following states: IN, KY, MO & TN.
    Amount recalled
    168 pints & 31/3 gallon containers
    Status
    Ended Feb 15, 2018 (FDA lists it as terminated)
    FDA recall number
    F-3448-2017
  3. ENDEDClass II ยท ModerateRecalled Jul 21, 2017

    The Comfy Cow Intense Dark Chocolate Ice Cream 1 pint

    The firm is recalling various brands of ice cream due to E. coli & high Coliform Bacteria counts in various products.

    Koogee-Queen Anne, LLC ยท Louisville, KY

    Where it was sold: Product was shipped to the following states: IN, KY, MO & TN.

    Show details
    Product, as FDA describes it
    The Comfy Cow Intense Dark Chocolate Ice Cream 1 pint
    Reason, in FDA's words
    The firm is recalling various brands of ice cream due to E. coli & high Coliform Bacteria counts in various products.
    Codes on the package
    Lot: IDC1B06212017A1, Best By: 03/23/2018
    Where it was sold
    Product was shipped to the following states: IN, KY, MO & TN.
    Amount recalled
    12 pints
    Status
    Ended Feb 15, 2018 (FDA lists it as terminated)
    FDA recall number
    F-3449-2017
  4. ENDEDClass II ยท ModerateRecalled Jul 21, 2017

    The Comfy Cow Salted Caramel Ice Cream 1 pint

    The firm is recalling various brands of ice cream due to E. coli & high Coliform Bacteria counts in various products.

    Koogee-Queen Anne, LLC ยท Louisville, KY

    Where it was sold: Product was shipped to the following states: IN, KY, MO & TN.

    Show details
    Product, as FDA describes it
    The Comfy Cow Salted Caramel Ice Cream 1 pint
    Reason, in FDA's words
    The firm is recalling various brands of ice cream due to E. coli & high Coliform Bacteria counts in various products.
    Codes on the package
    Lot: SCR1CR07122017A1, Best By: 04/13/2018
    Where it was sold
    Product was shipped to the following states: IN, KY, MO & TN.
    Amount recalled
    45 pints
    Status
    Ended Feb 15, 2018 (FDA lists it as terminated)
    FDA recall number
    F-3450-2017
  5. ENDEDClass II ยท ModerateRecalled Jul 21, 2017

    The Comfy Cow Strawberry Fields Forever Ice Cream 1 pint

    The firm is recalling various brands of ice cream due to E. coli & high Coliform Bacteria counts in various products.

    Koogee-Queen Anne, LLC ยท Louisville, KY

    Where it was sold: Product was shipped to the following states: IN, KY, MO & TN.

    Show details
    Product, as FDA describes it
    The Comfy Cow Strawberry Fields Forever Ice Cream 1 pint
    Reason, in FDA's words
    The firm is recalling various brands of ice cream due to E. coli & high Coliform Bacteria counts in various products.
    Codes on the package
    Lot: SFF1CR06192017A1, Best By: 03/21/2018
    Where it was sold
    Product was shipped to the following states: IN, KY, MO & TN.
    Amount recalled
    453 pints
    Status
    Ended Feb 15, 2018 (FDA lists it as terminated)
    FDA recall number
    F-3451-2017
  6. ENDEDClass II ยท ModerateRecalled Jun 13, 2017

    BAKEMARK CANADA White Cross Topping Mix 10 lb 4.54 kg; BakeMark NDS Item Code: 50623; UPC: 0 64278 5...

    Product may be contaminated with E. coli O121.

    Bakemark Ingredients Canada Lt ยท Calgary, Alberta

    Where it was sold: CT NJ

    UPC 064278506237
    Show details
    Product, as FDA describes it
    BAKEMARK CANADA White Cross Topping Mix 10 lb 4.54 kg; BakeMark NDS Item Code: 50623; UPC: 0 64278 50623 7
    Reason, in FDA's words
    Product may be contaminated with E. coli O121.
    Codes on the package
    Lot: 4-16-326-01 and 4-16-326-02
    Where it was sold
    CT NJ
    Amount recalled
    454 units
    Status
    Ended Aug 10, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2138-2017
  7. ENDEDClass I ยท Most seriousRecalled Jun 8, 2017

    Robin Hood All Purpose Flour 1.8kg retial Pouch 6/1.8kg retial pouches per wholesale case

    may contain E. coli O121

    Element Food Solutions ยท Hodgkins, IL

    Where it was sold: CANADA

    UPC 059000018232
    Show details
    Product, as FDA describes it
    Robin Hood All Purpose Flour 1.8kg retial Pouch 6/1.8kg retial pouches per wholesale case
    Reason, in FDA's words
    may contain E. coli O121
    Codes on the package
    UPC Code 059000018232 Pouch Code; Case Code; Best Before Date.: 6 334 623 05 BB/MA 2018 MA 29; 6 334 623 05 BB/MA 2018-05-29; 5/29/2018. 6 335 623 05 BB/MA 2018 MA 30; 6 335 623 05 BB/MA 2018-05-30; 5/30/2018. 6 336 623 05 BB/MA 2018 JN 01; 6 336 623 05 BB/MA 2018-06-01; 6/1/2018. 6 337 623 05 BB/MA 2018 JN 02; 6 337 623 05 BB/MA 2018-06-02; 6/2/2018. 7 024 623 05 BB/MA 2018 JL 24; 7 024 623 05 BB/MA 2018-07-24; 7/24/2018. 7 026 623 05 BB/MA 2018 JL 26; 7 026 623 05 BB/MA 2018-07-26; 7/26/2018.
    Where it was sold
    CANADA
    Amount recalled
    6,533 cases
    Status
    Ended Apr 29, 2020 (FDA lists it as terminated)
    FDA recall number
    F-2453-2017
  8. ENDEDClass I ยท Most seriousRecalled Jun 2, 2017

    PRIMO MOLINO ITALIAN STYLE ENRICHED FLOUR, 50 lb, Packaged in paper bags, Store at Ambient Temperatu...

    Primo Molino Italian Style Flour may be contaminated with E. coli O121.

    Ardent Mills, LLC ยท Denver, CO

    Where it was sold: Distributed to three locations. No Govt/VA/Military consignees. 380 bags to CH Gunther ( Pizza Blends) 1541 VERNON ST Kansas City MO 11/21/16 112 bags shipped to Nations Pizza...

    Show details
    Product, as FDA describes it
    PRIMO MOLINO ITALIAN STYLE ENRICHED FLOUR, 50 lb, Packaged in paper bags, Store at Ambient Temperature, produced on 10/31/16, Product code 15031
    Reason, in FDA's words
    Primo Molino Italian Style Flour may be contaminated with E. coli O121.
    Codes on the package
    Lot code- 6 305 SK
    Where it was sold
    Distributed to three locations. No Govt/VA/Military consignees. 380 bags to CH Gunther ( Pizza Blends) 1541 VERNON ST Kansas City MO 11/21/16 112 bags shipped to Nations Pizza 601 E ALGONQUIN RD SCHAUMBURG IL on 1/17/2017 5 bags shipped to AK Crust 1326 CORNELL RD Green Bay WI 11/30/16
    Amount recalled
    487 bags
    Status
    Ended Aug 7, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2426-2017
  9. ENDEDClass I ยท Most seriousRecalled May 26, 2017

    Flour sold under the following brands: Golden Temple Durum Atta Flour Blend, 20LB, DISTRIBUTED BY: S...

    The firm was notified by their Co-packer that the product may be contaminated with E. coli.

    Smucker Foods of Canada Co. ยท Markham, N/A

    Where it was sold: Product was sent to the following states: CA, FL, GA, IL, KS, MD, MI, NC, NJ, NY, TX, VA & WA.

    UPC 059000415567UPC 051179160309UPC 020843100019
    Show details
    Product, as FDA describes it
    Flour sold under the following brands: Golden Temple Durum Atta Flour Blend, 20LB, DISTRIBUTED BY: SMUCKER FOODS OF CANADA CORP., MARKHAM, ON L3R 0P3 PRODUCT OF CANADA UPC 0 59000 41556 7, Swad Durum Atta Flour, 20 LB MILLED FOR: RAJA FOODS 8110 N. St. Louis Avenue Skokie, IL 60075 57-03, 48th Street Maspeth, NY 11378 PRODUCT OF CANADA, UPC 0 51179 16030 9 & Maya Durum Wheat Atta Flour, 20 LB, DISTRIBUTED BY: MAYA OVERSEAS FOODS INC. 48-85 MASPETH AVENUE MASPETH, N.Y. 11378 Product of Canada UPC 0 20843 10001 9 Ingredients: Durum Wheat Atta Flour, Durum Wheat Bran, Wheat Flour, Niacin, Reduced Iron, Thiamin Mononitrate, Riboflavin, Folic Acid.
    Reason, in FDA's words
    The firm was notified by their Co-packer that the product may be contaminated with E. coli.
    Codes on the package
    Maya - Lot Numbers, 6286548, & Lot Numbers, 6287548; Swad - Lot Numbers, 6294548, Lot Numbers, 6299548, Lot Numbers, 6300548, & Lot Numbers, 6308548, Golden Temple - Lot Numbers, 6287548, Best If Used By: 18-Jan, Lot Numbers, 6288548, Best If Used By: 18-Jan, Lot Numbers, 6294548, Best If Used By: 18-Jan, Lot Numbers, 6295548, Best If Used By: 18-Jan, Lot Numbers, 6300548, Best If Used By: 18-Jan, Lot Numbers, 6301548, Best If Used By: 18-Jan, Lot Numbers, 6306548, Best If Used By: 18-Jan, Lot Numbers, 6307548, Best If Used By: 18-Feb & Lot Numbers, 6308548, Best If Used By: 18-Feb
    Where it was sold
    Product was sent to the following states: CA, FL, GA, IL, KS, MD, MI, NC, NJ, NY, TX, VA & WA.
    Amount recalled
    GT=24,963 cs/2/20 lb bags, Swad =17,241/20 lb bags & Maya = 5,974/20 lb bags
    Status
    Ended Sep 11, 2018 (FDA lists it as terminated)
    FDA recall number
    F-2424-2017
  10. ENDEDClass I ยท Most seriousRecalled May 26, 2017

    Golden Temple No. 1 Fine Durum Atta Flour Blend NET WT 20 LB INGREDIENTS: DURUM WHEAT FLOUR, DURUM W...

    The firm was notified by their Co-packer that the product may be contaminated with E. coli.

    Smucker Foods of Canada Co. ยท Markham, N/A

    Where it was sold: Product was sent to the following states: CA, FL, GA, IL, KS, MD, MI, NC, NJ, NY, TX, VA & WA.

    UPC 059000405407
    Show details
    Product, as FDA describes it
    Golden Temple No. 1 Fine Durum Atta Flour Blend NET WT 20 LB INGREDIENTS: DURUM WHEAT FLOUR, DURUM WHEAT BRAN, WHEAT FLOUR, NIACIN, REDUCED IRON, THIAMIN MONONITRATE, RIBOFLAVIN, FOLIC ACID. DISTRIBUTED BY: SMUCKER FOODS OF CANADA CORP., MARKHAM, ON L3R 0P3 PRODUCT OF CANADA UPC 0 59000 40540
    Reason, in FDA's words
    The firm was notified by their Co-packer that the product may be contaminated with E. coli.
    Codes on the package
    Lot Number, 6286548, Best If Used By 18-Jan & Lot Number, 6299548, Best If Used By 18-Jan
    Where it was sold
    Product was sent to the following states: CA, FL, GA, IL, KS, MD, MI, NC, NJ, NY, TX, VA & WA.
    Amount recalled
    2,492cs/2/20 lb bags
    Status
    Ended Sep 11, 2018 (FDA lists it as terminated)
    FDA recall number
    F-2425-2017
  11. ENDEDClass II ยท 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. ยท 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
  12. ENDEDClass II ยท 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. ยท 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
  13. ENDEDClass II ยท 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. ยท 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
  14. ENDEDClass II ยท 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. ยท 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
  15. ENDEDClass II ยท 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. ยท 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
  16. ENDEDClass II ยท 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. ยท 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
  17. ENDEDClass I ยท 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 ยท 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
  18. ENDEDClass II ยท 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 ยท 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
  19. ENDEDClass II ยท 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 ยท 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
  20. ENDEDClass II ยท 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 ยท 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

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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.