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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

7,651 recalls ยท showing 2,321 to 2,340

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  1. ENDEDClass II ยท ModerateRecalled Jun 22, 2021

    Milo's Sauce 5 gallon pails 24 pails per pallet

    Undeclared Fish Allergen

    Southern Classic Food Group LLC ยท Brundidge, AL

    Where it was sold: Single Consignee located in AL

    Show details
    Product, as FDA describes it
    Milo's Sauce 5 gallon pails 24 pails per pallet
    Reason, in FDA's words
    Undeclared Fish Allergen
    Codes on the package
    Product Number : 7850; Lot Numbers : 1148, 1169, 1165, 1158
    Where it was sold
    Single Consignee located in AL
    Amount recalled
    597 Total
    Status
    Ended Jul 8, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0769-2021
  2. ENDEDClass II ยท ModerateRecalled Jun 21, 2021

    Trader Joes Dark Chocolate Almond Butter Cup, 1.4 oz. (2-20-gram cups per pack), PVC Pouch, 72 packs...

    Potential undeclared peanut allergen.

    Bazzini LLC ยท Allentown, PA

    Where it was sold: The recall product was distributed to the following states, PA, IL, CT, CA, WA, TX FL

    Show details
    Product, as FDA describes it
    Trader Joes Dark Chocolate Almond Butter Cup, 1.4 oz. (2-20-gram cups per pack), PVC Pouch, 72 packs per case; 2 cups per pack .
    Reason, in FDA's words
    Potential undeclared peanut allergen.
    Codes on the package
    Apr 05 2022 1B095 Apr 05 2022 2B095 Apr 06 2022 1B096 Apr 06 2022 2B096 Apr 07 2022 1B097 Apr 07 2022 2B097
    Where it was sold
    The recall product was distributed to the following states, PA, IL, CT, CA, WA, TX FL
    Amount recalled
    2816 Cases
    Status
    Ended Oct 14, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0772-2021
  3. ENDEDClass II ยท ModerateRecalled Jun 21, 2021

    Living Free "Adult Extra" multi-vitamin, 100 or 500 capsules per bottle. Product is packed in white...

    Label declares lecithin but does not declare soy lecithin.

    Bea Lydeckers Naturals Inc ยท Oregon City, OR

    Where it was sold: distributed nationwide.

    Show details
    Product, as FDA describes it
    Living Free "Adult Extra" multi-vitamin, 100 or 500 capsules per bottle. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "**Living Free Adult Extra***Natural Vitamin Mineral Herbal Glandular Supplements***Formulated and Manufactured by BEA LYDECKER's NATURALS Oregon City, OR*** 503-631-8589***".
    Reason, in FDA's words
    Label declares lecithin but does not declare soy lecithin.
    Codes on the package
    No lot code or expiration date listed on label.
    Where it was sold
    distributed nationwide.
    Amount recalled
    Firm did not provide
    Status
    Ended Feb 24, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0776-2021
  4. ENDEDClass II ยท ModerateRecalled Jun 21, 2021

    Living Free Heart/Blood Vessel Dietary Supplement, 100 or 500 capsules per bottle. Product is pack...

    Label declares lecithin but does not declare soy lecithin.

    Bea Lydeckers Naturals Inc ยท Oregon City, OR

    Where it was sold: distributed nationwide.

    Show details
    Product, as FDA describes it
    Living Free Heart/Blood Vessel Dietary Supplement, 100 or 500 capsules per bottle. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Heart/Blood Vessel Dietary Supplement***Glandular Herbal & Vitamin Blend***Formulated by Beatrice Lydecker ***Manufactured by Bea Lydecker's Naturals Oregon City, OR*** 503-631-8589***".
    Reason, in FDA's words
    Label declares lecithin but does not declare soy lecithin.
    Codes on the package
    No lot code or expiration date listed on label.
    Where it was sold
    distributed nationwide.
    Amount recalled
    Firm did not provide
    Status
    Ended Feb 24, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0777-2021
  5. ENDEDClass II ยท ModerateRecalled Jun 21, 2021

    Living Free Immune Dietary Supplement, 100 and 500 capsules per bottles. Product is packed in white...

    Label declares lecithin but does not declare soy lecithin.

    Bea Lydeckers Naturals Inc ยท Oregon City, OR

    Where it was sold: distributed nationwide.

    Show details
    Product, as FDA describes it
    Living Free Immune Dietary Supplement, 100 and 500 capsules per bottles. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Immune Dietary Supplement***Glandular and Herbal Supplement***Formulated by Beatrice Lydecker ***Manufactured by Bea Lydecker's Naturals Oregon City, OR*** 503-631-8589***".
    Reason, in FDA's words
    Label declares lecithin but does not declare soy lecithin.
    Codes on the package
    No lot code or expiration date listed on label.
    Where it was sold
    distributed nationwide.
    Amount recalled
    Firm did not provide
    Status
    Ended Feb 24, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0778-2021
  6. ENDEDClass II ยท ModerateRecalled Jun 21, 2021

    Living Free Lung & Joint Congestion Herbal Dietary Supplement, 100 and 500 capsules per bottles. Pr...

    Label declares lecithin but does not declare soy lecithin.

    Bea Lydeckers Naturals Inc ยท Oregon City, OR

    Where it was sold: distributed nationwide.

    Show details
    Product, as FDA describes it
    Living Free Lung & Joint Congestion Herbal Dietary Supplement, 100 and 500 capsules per bottles. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Lung & Joint Congestion Herbal Dietary Supplement***Glandular, Herbal & Vitamin Supplement***Formulated by Beatrice Lydecker ***Manufactured by Bea Lydecker's Naturals Oregon City, OR*** 503-631-8589***".
    Reason, in FDA's words
    Label declares lecithin but does not declare soy lecithin.
    Codes on the package
    No lot code or expiration date listed on label.
    Where it was sold
    distributed nationwide.
    Amount recalled
    Firm did not provide
    Status
    Ended Feb 24, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0779-2021
  7. ENDEDClass II ยท ModerateRecalled Jun 21, 2021

    Living Free Nerve & Muscle Herbal Dietary Supplement, 100 and 500 capsules per bottles. Product is ...

    Label declares lecithin but does not declare soy lecithin.

    Bea Lydeckers Naturals Inc ยท Oregon City, OR

    Where it was sold: distributed nationwide.

    Show details
    Product, as FDA describes it
    Living Free Nerve & Muscle Herbal Dietary Supplement, 100 and 500 capsules per bottles. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Nerve & Muscle Herbal Dietary Supplement***Herbal and Glandular Supplement***Formulated by Beatrice Lydecker ***Manufactured by Bea Lydecker's Naturals Oregon City, OR*** 503-631-8589***".
    Reason, in FDA's words
    Label declares lecithin but does not declare soy lecithin.
    Codes on the package
    No lot code or expiration date listed on label.
    Where it was sold
    distributed nationwide.
    Amount recalled
    Firm did not provide
    Status
    Ended Feb 24, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0780-2021
  8. ENDEDClass II ยท ModerateRecalled Jun 21, 2021

    Living Free Nerve & Muscle Plus Cetyl-Myristoleate Herbal and Glandular Supplement, 180 and 500 caps...

    Label declares lecithin but does not declare soy lecithin.

    Bea Lydeckers Naturals Inc ยท Oregon City, OR

    Where it was sold: distributed nationwide.

    Show details
    Product, as FDA describes it
    Living Free Nerve & Muscle Plus Cetyl-Myristoleate Herbal and Glandular Supplement, 180 and 500 capsules per bottles. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Nerve & Muscle Plus Cetyl-Myristoleate *** Herbal and Glandular Supplement***Formulated by Beatrice Lydecker ***Manufactured by Bea Lydecker's Naturals Oregon City, OR***".
    Reason, in FDA's words
    Label declares lecithin but does not declare soy lecithin.
    Codes on the package
    No lot code or expiration date listed on label.
    Where it was sold
    distributed nationwide.
    Amount recalled
    Firm did not provide
    Status
    Ended Feb 24, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0781-2021
  9. ENDEDClass II ยท ModerateRecalled Jun 18, 2021

    JUST Egg Inspired by America Roasted Potato, Dill, Chives, Red Bell Pepper, Black Pepper 4 Sous Vide...

    Undeclared egg and milk

    Cuisine Solutions ยท Sterling, VA

    Where it was sold: Distributed nationwide

    UPC 005044025033UPC 705044025032UPC 10705044025039
    Show details
    Product, as FDA describes it
    JUST Egg Inspired by America Roasted Potato, Dill, Chives, Red Bell Pepper, Black Pepper 4 Sous Vide Plant Egg Bites NET WT8.4OZ (238g). UPC: 0504402503, Expiration dates 2/22/2022, 3/1/2022, 3/8/2022, 2/22/2022, and 4/6/2022. 16 cartons per corrugated case, Carton GTIN 7 05044 02503 2, Case Bar Code 10 7050 440 25039
    Reason, in FDA's words
    Undeclared egg and milk
    Codes on the package
    82530, 82625, 82769, and 83367
    Where it was sold
    Distributed nationwide
    Amount recalled
    4633 cases
    Status
    Ended Mar 30, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0743-2021
  10. ENDEDClass II ยท ModerateRecalled Jun 18, 2021

    JUST Egg Inspired by Mexico Roasted Poblanos, Ancho Chilli Powder, Black Beans, Corn, Lime 4 Sous Vi...

    Undeclared egg and milk

    Cuisine Solutions ยท Sterling, VA

    Where it was sold: Distributed nationwide

    UPC 005044025170UPC 705044025179
    Show details
    Product, as FDA describes it
    JUST Egg Inspired by Mexico Roasted Poblanos, Ancho Chilli Powder, Black Beans, Corn, Lime 4 Sous Vide Plant Egg Bites NET WT8.4OZ (238g). UPC: 0504402517, Expiration dates 3/3/2022, 3/29/2022, 3/10/2022, and 4/7/2022. 16 cartons per corrugated case, Carton GTIN 7 05044 02517 9 Case Bar Code 10 7054 402 5176
    Reason, in FDA's words
    Undeclared egg and milk
    Codes on the package
    82543, 82784, and 83368
    Where it was sold
    Distributed nationwide
    Amount recalled
    4339 cases
    Status
    Ended Mar 30, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0744-2021
  11. ENDEDClass II ยท ModerateRecalled Jun 18, 2021

    JUST Egg Inspired by India Curry, Broccoli, Cauliflower, Coconut Milk, Lemongrass 4 Sous Vide Plant ...

    Undeclared egg and milk

    Cuisine Solutions ยท Sterling, VA

    Where it was sold: Distributed nationwide

    UPC 005044025118UPC 705044025117UPC 10705044025114
    Show details
    Product, as FDA describes it
    JUST Egg Inspired by India Curry, Broccoli, Cauliflower, Coconut Milk, Lemongrass 4 Sous Vide Plant Egg Bites NET WT8.4OZ (238g). UPC: 0504402511, Expiration dates 3/5/2022, 3/31/2022, and 4/9/2022.16 cartons per corrugated case, Carton GTIN 7 05044 02511 7 Case Bar Code 10 7050 440 25114
    Reason, in FDA's words
    Undeclared egg and milk
    Codes on the package
    82541, 83232, and 83369
    Where it was sold
    Distributed nationwide
    Amount recalled
    780 cases
    Status
    Ended Mar 30, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0745-2021
  12. ENDEDClass II ยท ModerateRecalled Jun 18, 2021

    JUST Egg Inspired by Japan Portobello, Mushrooms, Sweet Potatos, Furikake, Soy 4 Sous Vide Plant Egg...

    Undeclared egg and milk

    Cuisine Solutions ยท Sterling, VA

    Where it was sold: Distributed nationwide

    UPC 005044025231UPC 705044025230
    Show details
    Product, as FDA describes it
    JUST Egg Inspired by Japan Portobello, Mushrooms, Sweet Potatos, Furikake, Soy 4 Sous Vide Plant Egg Bites NET WT8.4OZ (238g). UPC: 0504402523, Expiration dates 3/5/2022, 3/31/2022, and 4/9/2022.16 cartons per corrugated case, Carton GTIN 7 05044 02523 0, Case Bar Code 10 750 440 25237
    Reason, in FDA's words
    Undeclared egg and milk
    Codes on the package
    82790 and 83231
    Where it was sold
    Distributed nationwide
    Amount recalled
    320 units
    Status
    Ended Mar 30, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0746-2021
  13. ENDEDClass II ยท ModerateRecalled Jun 14, 2021

    Somerdale Red Dragon Cheddar Cheese, cut and repacked in plastic cheese wrap by Wegmans and sold by ...

    Cheese label does not declare wheat from ale wash

    Wegmans Food Markets, Inc. ยท Rochester, NY

    Where it was sold: Maryland, Massachusetts, New Jersey, New York, North Carolina, Pennsylvania, Virginia

    Show details
    Product, as FDA describes it
    Somerdale Red Dragon Cheddar Cheese, cut and repacked in plastic cheese wrap by Wegmans and sold by the pound.
    Reason, in FDA's words
    Cheese label does not declare wheat from ale wash
    Codes on the package
    All product packed on April 23, 2021, or later
    Where it was sold
    Maryland, Massachusetts, New Jersey, New York, North Carolina, Pennsylvania, Virginia
    Amount recalled
    1299 lbs.
    Status
    Ended May 19, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0766-2021
  14. ENDEDClass II ยท ModerateRecalled Jun 9, 2021

    Su Cocina Pan Molido bread crumbs in 8 oz. packages. UPC 6 79790 05912 5. The label of 8 oz. packa...

    Label declares whey but does not declare milk.

    Dominguez Foods of Washington, Inc. ยท Zillah, WA

    Where it was sold: Washington and Oregon

    UPC 679790059125
    Show details
    Product, as FDA describes it
    Su Cocina Pan Molido bread crumbs in 8 oz. packages. UPC 6 79790 05912 5. The label of 8 oz. package is read in parts: "***Plain Bread Crumbs *** Su Cocina Pan Molido***INGREDIENTS: Enriched wheat Flour ***Corn Starch, Corn Syrup, Water, Contains 2% or less of the following: Soybean Oil and/or Canola Oil, Salt, Yeast, Whey, Soy Flour ***DOMINGUEZ FOODS OF WASHINGTON ***Zillah, Washington***".
    Reason, in FDA's words
    Label declares whey but does not declare milk.
    Codes on the package
    None.
    Where it was sold
    Washington and Oregon
    Amount recalled
    15 cases (or 180/8oz. packages)
    Status
    Ended Jul 13, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0682-2021
  15. ENDEDClass I ยท Most seriousRecalled Jun 4, 2021

    Tulkoff Spicy Kimchi Aioli, 18 fl oz Clear Plastic Squeeze bottle, item number 098001, lot number 09...

    Tulkoff Food Products Inc., 2229 Van Deman Street, Baltimore MD 21224 has initiated a recall of Tulkoff Spicy Kimchi Aioli, 18 fl oz Clear Plastic Squ...

    Tulkoff Food Products, Inc. ยท Baltimore, MD

    Where it was sold: The product was distributed domestically to the following States: NJ, PA and MD.

    Show details
    Product, as FDA describes it
    Tulkoff Spicy Kimchi Aioli, 18 fl oz Clear Plastic Squeeze bottle, item number 098001, lot number 09.18.2021M, 8 bottles per case, keep refrigerated
    Reason, in FDA's words
    Tulkoff Food Products Inc., 2229 Van Deman Street, Baltimore MD 21224 has initiated a recall of Tulkoff Spicy Kimchi Aioli, 18 fl oz Clear Plastic Squeeze bottle, item number 098001, lot number 09.18.2021M because of undeclared allergens (Soy, Wheat)
    Codes on the package
    item number 098001, lot number 09.18.2021M
    Where it was sold
    The product was distributed domestically to the following States: NJ, PA and MD.
    Amount recalled
    140 Cases
    Status
    Ended Oct 7, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0756-2021
  16. ENDEDClass II ยท ModerateRecalled Jun 2, 2021

    Hix Sauces, Buffalo Wing Sauce, Original Spice, Net Wt. 12.5 oz (355g)

    Product label declares butter but does not list milk.

    Hix Foods, Inc. ยท Loxahatchee, FL

    Where it was sold: FL

    Show details
    Product, as FDA describes it
    Hix Sauces, Buffalo Wing Sauce, Original Spice, Net Wt. 12.5 oz (355g)
    Reason, in FDA's words
    Product label declares butter but does not list milk.
    Codes on the package
    Lot # 071320 HIXWG Exp. Date 7/13/22
    Where it was sold
    FL
    Amount recalled
    340-350 cases/6 jars ea.
    Status
    Ended Jan 27, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0670-2021
  17. ENDEDClass I ยท Most seriousRecalled Jun 2, 2021

    Brown Rice Quinoa Farro, Fully Cooked Net Wt. 24 lbs, Item # 617322

    Farro-containing products fail to declare the major food allergen Wheat

    Savor Brands LLC. ยท Chesterfield, MO

    Where it was sold: Distributed to a distributor in Illinois for further distribution to restaurants.

    Show details
    Product, as FDA describes it
    Brown Rice Quinoa Farro, Fully Cooked Net Wt. 24 lbs, Item # 617322
    Reason, in FDA's words
    Farro-containing products fail to declare the major food allergen Wheat
    Codes on the package
    All codes
    Where it was sold
    Distributed to a distributor in Illinois for further distribution to restaurants.
    Amount recalled
    4,597 cases
    Status
    Ended Dec 2, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0671-2021
  18. ENDEDClass I ยท Most seriousRecalled Jun 2, 2021

    Farro, Fully Cooked Net Wt. 24 lbs, Item # 641901

    Farro-containing products fail to declare the major food allergen Wheat

    Savor Brands LLC. ยท Chesterfield, MO

    Where it was sold: Distributed to a distributor in Illinois for further distribution to restaurants.

    Show details
    Product, as FDA describes it
    Farro, Fully Cooked Net Wt. 24 lbs, Item # 641901
    Reason, in FDA's words
    Farro-containing products fail to declare the major food allergen Wheat
    Codes on the package
    All codes
    Where it was sold
    Distributed to a distributor in Illinois for further distribution to restaurants.
    Amount recalled
    1,138 cases
    Status
    Ended Dec 2, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0672-2021
  19. ENDEDClass II ยท ModerateRecalled Jun 2, 2021

    O'Brien's Own Gourmet Granola, blueberry muffin, Net Wt. 12 OZ , UPC 6 09132 49665 3, Manufactured a...

    Three flavors of 3X Protein granola are labeled to contain whey, but do not declare milk on the label.

    Browns Granola Company, LLC ยท Center Point, IA

    Where it was sold: Distributed to grocery stores in Iowa and directly to consumers at farmer's markets.

    UPC 609132496653
    Show details
    Product, as FDA describes it
    O'Brien's Own Gourmet Granola, blueberry muffin, Net Wt. 12 OZ , UPC 6 09132 49665 3, Manufactured and Distributed by O'Brien's Own Gourmet Granola, Center Point, IA.
    Reason, in FDA's words
    Three flavors of 3X Protein granola are labeled to contain whey, but do not declare milk on the label.
    Codes on the package
    all best buy dates
    Where it was sold
    Distributed to grocery stores in Iowa and directly to consumers at farmer's markets.
    Amount recalled
    282 bags (total)
    Status
    Ended Aug 12, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0679-2021
  20. ENDEDClass II ยท ModerateRecalled Jun 2, 2021

    O'Brien's Own Gourmet Granola, busy bee's honey & oat, Net Wt. 12 OZ , UPC 6 09132 49667 7; Manufact...

    Three flavors of 3X Protein granola are labeled to contain whey, but do not declare milk on the label.

    Browns Granola Company, LLC ยท Center Point, IA

    Where it was sold: Distributed to grocery stores in Iowa and directly to consumers at farmer's markets.

    UPC 609132496677
    Show details
    Product, as FDA describes it
    O'Brien's Own Gourmet Granola, busy bee's honey & oat, Net Wt. 12 OZ , UPC 6 09132 49667 7; Manufactured and Distributed by O'Brien's Own Gourmet Granola, Center Point, IA.
    Reason, in FDA's words
    Three flavors of 3X Protein granola are labeled to contain whey, but do not declare milk on the label.
    Codes on the package
    all best buy dates
    Where it was sold
    Distributed to grocery stores in Iowa and directly to consumers at farmer's markets.
    Amount recalled
    282 bags (total)
    Status
    Ended Aug 12, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0680-2021

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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.