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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

7,366 ended recalls · showing 5,301 to 5,320

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  1. ENDEDClass II · ModerateRecalled Sep 3, 2015

    French Burnt Peanuts, NET WEIGHT 8 OZ (227g) Old Time Candy.com Distributed by Old Time Candy Compan...

    The firm has the incorrect ingredient statement on the package. The ingredient statement fails to list the allergen "Peanuts", Sugar, artificial colo...

    Old Time Candy · Olmsted Falls, OH

    Where it was sold: Product was shipped to the following states: AL, AR, CA, CO, CT, FL,HI, IL, KS, KY, MA, MD, ME, MI, MN, MO, MS, NJ, NY, OK, OR, PA, SC, TN, TX, VA, VT, WA & WI.

    Show details
    Product, as FDA describes it
    French Burnt Peanuts, NET WEIGHT 8 OZ (227g) Old Time Candy.com Distributed by Old Time Candy Company LaGrange, OH 44050 www.oldtimecandy.com Ingredients: Dextrose, Citric Acid, Calcium Stearate, Artificial Flavors, Artificial Colors***. May Contain Milk And Soy.
    Reason, in FDA's words
    The firm has the incorrect ingredient statement on the package. The ingredient statement fails to list the allergen "Peanuts", Sugar, artificial colors (Red 3 & Blue 2), and Salt.
    Codes on the package
    There are no codes for this product
    Where it was sold
    Product was shipped to the following states: AL, AR, CA, CO, CT, FL,HI, IL, KS, KY, MA, MD, ME, MI, MN, MO, MS, NJ, NY, OK, OR, PA, SC, TN, TX, VA, VT, WA & WI.
    Amount recalled
    72 Containers
    Status
    Ended Jan 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0008-2016
    View in FDA's recall database
  2. ENDEDClass I · Most seriousRecalled Sep 2, 2015

    Hill Country Fare Natural Spring Water 1 GAL./3.78L container packaged in polyethylene jug

    Possible undeclared milk allergen.

    H E B Grocery Company, LP · Houston, TX

    Where it was sold: Texas

    Show details
    Product, as FDA describes it
    Hill Country Fare Natural Spring Water 1 GAL./3.78L container packaged in polyethylene jug
    Reason, in FDA's words
    Possible undeclared milk allergen.
    Codes on the package
    Best by date December 19, 2015
    Where it was sold
    Texas
    Amount recalled
    10,784 gallons
    Status
    Ended Oct 19, 2016 (FDA lists it as terminated)
    FDA recall number
    F-3256-2015
    View in FDA's recall database
  3. ENDEDClass I · Most seriousRecalled Aug 31, 2015

    Caramel Caribou Ice Cream, 3 gal, frozen in bulk round container.

    Product contains undeclared peanuts

    The Ice Cream Club, Inc. · Boynton Beach, FL

    Where it was sold: Nationwide to retail dipping stores, retirement communities, and one distributor: FL, GA, AL, TX, SC, RI, MI

    Show details
    Product, as FDA describes it
    Caramel Caribou Ice Cream, 3 gal, frozen in bulk round container.
    Reason, in FDA's words
    Product contains undeclared peanuts
    Codes on the package
    Lot 5333. No exp date indicated by firm
    Where it was sold
    Nationwide to retail dipping stores, retirement communities, and one distributor: FL, GA, AL, TX, SC, RI, MI
    Amount recalled
    68, 3 gal tubs
    Status
    Ended Feb 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-3251-2015
    View in FDA's recall database
  4. ENDEDClass I · Most seriousRecalled Aug 28, 2015

    DR. VENESSA'S FORMULAS ULTIMATE ANTIOXIDANT TABLETS DIETARY SUPPLEMENT, 120 count bottles, UPC 60685...

    The dietary supplement contains undeclared milk and crustacean shellfish based on FDA's inspection.

    VRVK Nutraceuticals, LLC · Orlando, FL

    Where it was sold: Nationwide and Puerto Rico

    UPC 606851551205
    Show details
    Product, as FDA describes it
    DR. VENESSA'S FORMULAS ULTIMATE ANTIOXIDANT TABLETS DIETARY SUPPLEMENT, 120 count bottles, UPC 606851551205
    Reason, in FDA's words
    The dietary supplement contains undeclared milk and crustacean shellfish based on FDA's inspection.
    Codes on the package
    Lot Number 132415 (expiration date 05/16) and Lot Number 141381 (expiration date 06/17)
    Where it was sold
    Nationwide and Puerto Rico
    Amount recalled
    3554 bottles
    Status
    Ended Jun 13, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0332-2016
    View in FDA's recall database
  5. ENDEDClass III · Low riskRecalled Aug 27, 2015

    Dough base/premix packaged in 30-lb. poly-lined cardboard boxes, manufactured under the following la...

    Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.

    Heartland Products Inc. · Des Moines, IA

    Where it was sold: Product was distributed in IA and IL. No foreign, military, or federal goverment distribution.

    Show details
    Product, as FDA describes it
    Dough base/premix packaged in 30-lb. poly-lined cardboard boxes, manufactured under the following labels: (1) Heartland Products, Inc. Fancy Breads Italian Base, 090108. Manufactured by Heartland Products, Inc., Des Moines, IA; and (2) Northern Lights Pizza, 090108, Manufactured by Heartland Products, Inc., Des Moines, IA.
    Reason, in FDA's words
    Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.
    Codes on the package
    (1) G0601 and (2) G0301
    Where it was sold
    Product was distributed in IA and IL. No foreign, military, or federal goverment distribution.
    Amount recalled
    (1) 24 - 30 lb. boxes and (2) 24- 30 lb. boxes
    Status
    Ended Apr 14, 2016 (FDA lists it as terminated)
    FDA recall number
    F-1075-2016
    View in FDA's recall database
  6. ENDEDClass III · Low riskRecalled Aug 27, 2015

    ILL RIVER #14 Bread Base, 050102, packaged in 28-lb. poly-lined cardboard boxes, Distributed by T.S....

    Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.

    Heartland Products Inc. · Des Moines, IA

    Where it was sold: Product was distributed in IA and IL. No foreign, military, or federal goverment distribution.

    Show details
    Product, as FDA describes it
    ILL RIVER #14 Bread Base, 050102, packaged in 28-lb. poly-lined cardboard boxes, Distributed by T.S. Products, Inc.
    Reason, in FDA's words
    Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.
    Codes on the package
    F1001-F1010, F1101-F1105, G1301-G1315, G1501-G1503, G2101-G2110, G2211-G2220, and G2401-G2409
    Where it was sold
    Product was distributed in IA and IL. No foreign, military, or federal goverment distribution.
    Amount recalled
    4,366 - 28 lb. boxes
    Status
    Ended Apr 14, 2016 (FDA lists it as terminated)
    FDA recall number
    F-1076-2016
    View in FDA's recall database
  7. ENDEDClass III · Low riskRecalled Aug 27, 2015

    Heartland Products, Inc. Roma's Italian Base, 120116, packaged in 50-lb. poly-lined cardboard boxes,...

    Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.

    Heartland Products Inc. · Des Moines, IA

    Where it was sold: Product was distributed in IA and IL. No foreign, military, or federal goverment distribution.

    Show details
    Product, as FDA describes it
    Heartland Products, Inc. Roma's Italian Base, 120116, packaged in 50-lb. poly-lined cardboard boxes, Manufactured by Heartland Products, Inc., Des Moines, IA.
    Reason, in FDA's words
    Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.
    Codes on the package
    G0602
    Where it was sold
    Product was distributed in IA and IL. No foreign, military, or federal goverment distribution.
    Amount recalled
    36 - 50 lb. boxes
    Status
    Ended Apr 14, 2016 (FDA lists it as terminated)
    FDA recall number
    F-1077-2016
    View in FDA's recall database
  8. ENDEDClass III · Low riskRecalled Aug 27, 2015

    ILL RIVER Sweet Dough Base, 050107, packaged in 50-lb. poly-lined cardboard boxes, Distributed by T....

    Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.

    Heartland Products Inc. · Des Moines, IA

    Where it was sold: Product was distributed in IA and IL. No foreign, military, or federal goverment distribution.

    Show details
    Product, as FDA describes it
    ILL RIVER Sweet Dough Base, 050107, packaged in 50-lb. poly-lined cardboard boxes, Distributed by T.S. Products, Inc.
    Reason, in FDA's words
    Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.
    Codes on the package
    G1501-G1503
    Where it was sold
    Product was distributed in IA and IL. No foreign, military, or federal goverment distribution.
    Amount recalled
    100- 50 lb. boxes
    Status
    Ended Apr 14, 2016 (FDA lists it as terminated)
    FDA recall number
    F-1078-2016
    View in FDA's recall database
  9. ENDEDClass III · Low riskRecalled Aug 27, 2015

    Turano Knead Dough Base, 70101, packaged in 42-lb. poly-lined cardboard boxes, Manufactured for Tura...

    Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.

    Heartland Products Inc. · Des Moines, IA

    Where it was sold: Product was distributed in IA and IL. No foreign, military, or federal goverment distribution.

    Show details
    Product, as FDA describes it
    Turano Knead Dough Base, 70101, packaged in 42-lb. poly-lined cardboard boxes, Manufactured for Turano Baking Co., Bolingbrook, IL.
    Reason, in FDA's words
    Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.
    Codes on the package
    G3101, G3102, H0501-H0508
    Where it was sold
    Product was distributed in IA and IL. No foreign, military, or federal goverment distribution.
    Amount recalled
    480 - 42 lb. boxes
    Status
    Ended Apr 14, 2016 (FDA lists it as terminated)
    FDA recall number
    F-1079-2016
    View in FDA's recall database
  10. ENDEDClass III · Low riskRecalled Aug 27, 2015

    Waveland Pancake and Waffle Mix, 030608, packaged in 25-lb. poly-lined cardboard boxes, Manufactured...

    Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.

    Heartland Products Inc. · Des Moines, IA

    Where it was sold: Product was distributed in IA and IL. No foreign, military, or federal goverment distribution.

    Show details
    Product, as FDA describes it
    Waveland Pancake and Waffle Mix, 030608, packaged in 25-lb. poly-lined cardboard boxes, Manufactured Heartland Products, Inc. Des Moines, IA 50321.
    Reason, in FDA's words
    Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.
    Codes on the package
    No lot number given; date of manufacture was 6/4/2015
    Where it was sold
    Product was distributed in IA and IL. No foreign, military, or federal goverment distribution.
    Amount recalled
    48 - 25 lb. boxes
    Status
    Ended Apr 14, 2016 (FDA lists it as terminated)
    FDA recall number
    F-1080-2016
    View in FDA's recall database
  11. ENDEDClass II · ModerateRecalled Aug 27, 2015

    America's Choice Straight Cut Sweet Potatoes Fries, Frozen 539 g in plastic bag. Distributed by: O...

    Undeclared gluten

    Russet House · Huntingdon, N/A

    Where it was sold: Connecticut, Delaware, Maryland, New Jersey, New York, and Pennsylvania.

    UPC 754807120255
    Show details
    Product, as FDA describes it
    America's Choice Straight Cut Sweet Potatoes Fries, Frozen 539 g in plastic bag. Distributed by: ONPOINT Inc. Montvale, NJ. Product of Canada UPC: 7 54807 12025 5
    Reason, in FDA's words
    Undeclared gluten
    Codes on the package
    Lot code: 221529 Exp: 09 feb 2017
    Where it was sold
    Connecticut, Delaware, Maryland, New Jersey, New York, and Pennsylvania.
    Amount recalled
    252 cases (12/case)
    Status
    Ended Oct 2, 2015 (FDA lists it as terminated)
    FDA recall number
    F-3247-2015
    View in FDA's recall database
  12. ENDEDClass II · ModerateRecalled Aug 27, 2015

    KAL Brand Amino Acid Complex UPC 021245 51610 1, Product #51610

    Undeclared allergen, casein is a disclosed ingredient, but the word milk not specifically noted on the ingredient list

    Nutraceutical International Corporation · Park City, UT

    Where it was sold: Nationwide to 34 states. No foreign/VA/govt/military.

    UPC 021245516101
    Show details
    Product, as FDA describes it
    KAL Brand Amino Acid Complex UPC 021245 51610 1, Product #51610
    Reason, in FDA's words
    Undeclared allergen, casein is a disclosed ingredient, but the word milk not specifically noted on the ingredient list
    Codes on the package
    UPC 021245516101, Product #51610, All lots with Use By Dates prior to January 2019.
    Where it was sold
    Nationwide to 34 states. No foreign/VA/govt/military.
    Amount recalled
    9501 bottles
    Status
    Ended Jul 26, 2016 (FDA lists it as terminated)
    FDA recall number
    F-3257-2015
    View in FDA's recall database
  13. ENDEDClass II · ModerateRecalled Aug 26, 2015

    The Great Gourmet 10/3 oz. Coconut seafood crab cake.

    The firm is missing important labeling information for three of its products (The Great Gourmet 10/3 oz. Coconut seafood crab cake, The Great Gourmet...

    The Great Gourmet Inc · Federalsburg, MD

    Where it was sold: Product is distributed thru QVC.

    Show details
    Product, as FDA describes it
    The Great Gourmet 10/3 oz. Coconut seafood crab cake.
    Reason, in FDA's words
    The firm is missing important labeling information for three of its products (The Great Gourmet 10/3 oz. Coconut seafood crab cake, The Great Gourmet 11/3 oz. Eastern Shore crab and shrimp cake and The Great Gourmet 32/1 oz. Cheesy Crab & Bacon Bites). The firms product labels do not list wheat in the ingredients statement or contains statement. Wheat is an allergen and can be harmful to indi
    Codes on the package
    Lot code 17415
    Where it was sold
    Product is distributed thru QVC.
    Amount recalled
    412 packs as of 8/26/2015
    Status
    Ended Aug 25, 2016 (FDA lists it as terminated)
    FDA recall number
    F-0177-2016
    View in FDA's recall database
  14. ENDEDClass II · ModerateRecalled Aug 26, 2015

    The Great Gourmet 11/3 oz. Eastern Shore crab and shrimp cake

    The firm is missing important labeling information for three of its products (The Great Gourmet 10/3 oz. Coconut seafood crab cake, The Great Gourmet ...

    The Great Gourmet Inc · Federalsburg, MD

    Where it was sold: Product is distributed thru QVC.

    Show details
    Product, as FDA describes it
    The Great Gourmet 11/3 oz. Eastern Shore crab and shrimp cake
    Reason, in FDA's words
    The firm is missing important labeling information for three of its products (The Great Gourmet 10/3 oz. Coconut seafood crab cake, The Great Gourmet 11/3 oz. Eastern Shore crab and shrimp cake and The Great Gourmet 32/1 oz. Cheesy Crab & Bacon Bites). The firms product labels do not list wheat in the ingredients statement or contains statement. Wheat is an allergen and can be harmful to indivi
    Codes on the package
    Lot code 17115
    Where it was sold
    Product is distributed thru QVC.
    Amount recalled
    644 packs as of 8/26/2015
    Status
    Ended Aug 25, 2016 (FDA lists it as terminated)
    FDA recall number
    F-0178-2016
    View in FDA's recall database
  15. ENDEDClass II · ModerateRecalled Aug 26, 2015

    The Great Gourmet 32/1 oz. Cheesy Crab & Bacon Bites .

    The firm is missing important labeling information for three of its products (The Great Gourmet 10/3 oz. Coconut seafood crab cake, The Great Gourmet ...

    The Great Gourmet Inc · Federalsburg, MD

    Where it was sold: Product is distributed thru QVC.

    Show details
    Product, as FDA describes it
    The Great Gourmet 32/1 oz. Cheesy Crab & Bacon Bites .
    Reason, in FDA's words
    The firm is missing important labeling information for three of its products (The Great Gourmet 10/3 oz. Coconut seafood crab cake, The Great Gourmet 11/3 oz. Eastern Shore crab and shrimp cake and The Great Gourmet 32/1 oz. Cheesy Crab & Bacon Bites). The firms product labels do not list wheat in the ingredients statement or contains statement. Wheat is an allergen and can be harmful to indivi
    Codes on the package
    Lot code 18115
    Where it was sold
    Product is distributed thru QVC.
    Amount recalled
    950 packs on 6/30/2015
    Status
    Ended Aug 25, 2016 (FDA lists it as terminated)
    FDA recall number
    F-0179-2016
    View in FDA's recall database
  16. ENDEDClass II · ModerateRecalled Aug 25, 2015

    Cumin Ground Product of India 50 lbs C/7784

    Cumin contains 8.0 ppm peanut allergen.

    SHAKTI GROUP USA LLC · New Brunswick, NJ

    Where it was sold: NY

    Show details
    Product, as FDA describes it
    Cumin Ground Product of India 50 lbs C/7784
    Reason, in FDA's words
    Cumin contains 8.0 ppm peanut allergen.
    Codes on the package
    Lot 55968
    Where it was sold
    NY
    Amount recalled
    39,450 lbs
    Status
    Ended Jun 19, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0339-2016
    View in FDA's recall database
  17. ENDEDClass I · Most seriousRecalled Aug 25, 2015

    Sam Mills Gluten Free Chocolate Chip Granola Bars with Dark Chocolate 5 bars/4.4oz Box (0.88oz each ...

    Undeclared milk

    Sam MillsUSA LLC · Boynton Beach, FL

    Where it was sold: AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, NC, NH, NJ, NY, OH, OK, OR, PA, TN, TX, UT, VA, WI, WV and District of Columbia

    Show details
    Product, as FDA describes it
    Sam Mills Gluten Free Chocolate Chip Granola Bars with Dark Chocolate 5 bars/4.4oz Box (0.88oz each bar)
    Reason, in FDA's words
    Undeclared milk
    Codes on the package
    Lot code: 10202014 exp. date 10/20/2015, Lot code: 11202014 exp. date 11/20/2015, Lot code: 12082014 exp. date 12/08/2015 (two shipments of this lot/exp on one day), Lot code: 02172015 exp. date 02/17/2016, Lot code: 02122015 exp. date 02/12/2016, Lot code: 02252015 exp. date 02/25/2016, Lot code: 02132015 exp. date 02/13/2016, Lot code: 02122015 exp. date 02/12/2016, Lot code: 04212015 exp. date 04/21/2016 (two shipments of this lot/exp on one day), and Lot code: 06162015 exp. date 06/16/2016.
    Where it was sold
    AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, NC, NH, NJ, NY, OH, OK, OR, PA, TN, TX, UT, VA, WI, WV and District of Columbia
    Amount recalled
    11,142 cases/ 6 boxes/ 5 bars (334,260 bars)
    Status
    Ended Feb 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-3237-2015
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled Aug 25, 2015

    Smoked Tofu is tofu sandwich on bread or a bun, enclosed in a clam shell with label

    Product contains wheat bun but the ingredients statement does NOT declare wheat and the Contains statement declared Soy only.

    Hillside Quickie Too · Tacoma, WA

    Where it was sold: distributed in Washington

    Show details
    Product, as FDA describes it
    Smoked Tofu is tofu sandwich on bread or a bun, enclosed in a clam shell with label
    Reason, in FDA's words
    Product contains wheat bun but the ingredients statement does NOT declare wheat and the Contains statement declared Soy only.
    Codes on the package
    08 30 (Use By August 30th) 09 02 (Use By Sept. 2nd)
    Where it was sold
    distributed in Washington
    Amount recalled
    did not provide
    Status
    Ended Dec 30, 2015 (FDA lists it as terminated)
    FDA recall number
    F-3238-2015
    View in FDA's recall database
  19. ENDEDClass II · ModerateRecalled Aug 25, 2015

    New York Deli Tofu is is tofu sandwich on bread or a bun, enclosed in a clam shell with label

    Product contains wheat bun but the ingredients statement does NOT declare wheat and the Contains statement declared Soy only.

    Hillside Quickie Too · Tacoma, WA

    Where it was sold: distributed in Washington

    Show details
    Product, as FDA describes it
    New York Deli Tofu is is tofu sandwich on bread or a bun, enclosed in a clam shell with label
    Reason, in FDA's words
    Product contains wheat bun but the ingredients statement does NOT declare wheat and the Contains statement declared Soy only.
    Codes on the package
    08 30 (Use By August 30th) 09 02 (Use By Sept. 2nd)
    Where it was sold
    distributed in Washington
    Amount recalled
    did not provide
    Status
    Ended Dec 30, 2015 (FDA lists it as terminated)
    FDA recall number
    F-3239-2015
    View in FDA's recall database
  20. ENDEDClass I · Most seriousRecalled Aug 24, 2015

    Trader Joe's Dark Chocolate covered Honey Grahams with Sea Salt NET Wt. 8oz. (227g) SKU #0055 0...

    Jo's Candies, LLC is recalling Trader Joe's Dark Chocolate covered Honey Grahams with Sea Salt because of undeclared milk.

    Jo'S Candies · Torrance, CA

    Where it was sold: U.S. distribution to the following; TX, CA, GA, IL, WA, and PA. No foreign distribution.

    Show details
    Product, as FDA describes it
    Trader Joe's Dark Chocolate covered Honey Grahams with Sea Salt NET Wt. 8oz. (227g) SKU #0055 0246 Product is packaged in 8oz. clear tubs.
    Reason, in FDA's words
    Jo's Candies, LLC is recalling Trader Joe's Dark Chocolate covered Honey Grahams with Sea Salt because of undeclared milk.
    Codes on the package
    UPC #00550246 "Best By" Dates 16 Mar 2016, 17 Mar 2016, 18 Mar 2016, 19 Mar 2016, 20 Mar 2016, 21 Mar 2016, 22 Mar 2016, 30 Mar 2016, 03 Apr 2016, 04 Apr 2016, 05 Apr 2016, 08 Apr 2016, 09 Apr 2016, 10 Apr 2016, 11 Apr 2016, 12 Apr 2016, 15 Apr 2016, 16 Apr 2016, 17 Apr 2016, 18 Apr 2016, 19 Apr 2016, 22 Apr 2016, 23 Apr 2016, 26 Apr 2016, 29 Apr 2016, 30 Apr 2016, 01 May 2016, 02 May 2016, 03 May 2016, 09 May 2016, 11 May 2016, 13 May 2016, 14 May 2016
    Where it was sold
    U.S. distribution to the following; TX, CA, GA, IL, WA, and PA. No foreign distribution.
    Amount recalled
    491,400 tubs
    Status
    Ended Feb 19, 2016 (FDA lists it as terminated)
    FDA recall number
    F-3227-2015
    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.