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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 2,061 to 2,080

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  1. ENDEDClass II · ModerateRecalled Jul 16, 2021

    f'real Made to Order Shake Base - 8 fl oz (237ml) cups Out packaging may read 'Smoothie-base' Lid ma...

    Shake base contains undeclare milk due to wrong outer-label stating product is Smoothie Base.

    Rich Products Corp · Buffalo, NY

    Where it was sold: IL, CA, PA, CO, NM

    Show details
    Product, as FDA describes it
    f'real Made to Order Shake Base - 8 fl oz (237ml) cups Out packaging may read 'Smoothie-base' Lid may read ' Shake-base' 12 individual cups packed into a shrink-wrapped pulp tray
    Reason, in FDA's words
    Shake base contains undeclare milk due to wrong outer-label stating product is Smoothie Base.
    Codes on the package
    Best by:10/13/2022 UPC code of 813993000977
    Where it was sold
    IL, CA, PA, CO, NM
    Amount recalled
    1,022 cases
    Status
    Ended May 19, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0818-2021
    View in FDA's recall database
  2. ENDEDClass II · ModerateRecalled Jul 16, 2021

    Assist and Amend Advanced Digestive Enzyme Formula, Dietary Supplement, 60 capsules per bottle, Manu...

    Product contained undeclared milk, wheat, and soy.

    New Dawn Nutrition, Inc. · Omaha, NE

    Where it was sold: Distributed to two retail consumers in the Omaha area.

    Show details
    Product, as FDA describes it
    Assist and Amend Advanced Digestive Enzyme Formula, Dietary Supplement, 60 capsules per bottle, Manufactured for and distributed by New Dawn Nutrition Omaha, NE
    Reason, in FDA's words
    Product contained undeclared milk, wheat, and soy.
    Codes on the package
    Lot #361551 Best By 2022
    Where it was sold
    Distributed to two retail consumers in the Omaha area.
    Amount recalled
    4 bottles
    Status
    Ended Aug 31, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0886-2021
    View in FDA's recall database
  3. ENDEDClass II · ModerateRecalled Jul 15, 2021

    Choujuki White Bread 6 slices: Net Wt. 13.9 oz. (374g) Ingredients: White Flour, Sugar, Margarine, ...

    Internal label review found that their labeling did not properly declare milk (sub ingredient of margarine) or as an allergen

    BLUE ROBINS INC · Torrance, CA

    Where it was sold: CA only

    Show details
    Product, as FDA describes it
    Choujuki White Bread 6 slices: Net Wt. 13.9 oz. (374g) Ingredients: White Flour, Sugar, Margarine, Yeast Extract, Salt, Rice Flour, Vinegar. Contains Wheat. Keep Frozen at or below 18 degrees C Distributed by Hatsune JPN Inc., Torrance, CA Product of Japan/
    Reason, in FDA's words
    Internal label review found that their labeling did not properly declare milk (sub ingredient of margarine) or as an allergen
    Codes on the package
    LOT# 220110, #220111, Item No. 115102, JAN CODE 4901820423269
    Where it was sold
    CA only
    Amount recalled
    277 Cartons (4,155 pkg)
    Status
    Ended Sep 1, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0807-2021
    View in FDA's recall database
  4. ENDEDClass II · ModerateRecalled Jul 2, 2021

    Caribbean Belize Spices Caribbean Rub, Net Wt. 3.5oz (99g) Plastic bottle with black cap Sold as sin...

    Undeclared Wheat Allergen

    Caribbean Belize LLC · Ville Platte, LA

    Where it was sold: CA, MI, SC, NY, IA, IL.

    Show details
    Product, as FDA describes it
    Caribbean Belize Spices Caribbean Rub, Net Wt. 3.5oz (99g) Plastic bottle with black cap Sold as single bottles
    Reason, in FDA's words
    Undeclared Wheat Allergen
    Codes on the package
    Lot Number 0304232106 Best By 04/23/24
    Where it was sold
    CA, MI, SC, NY, IA, IL.
    Amount recalled
    9 bottles
    Status
    Ended Oct 13, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0775-2021
    View in FDA's recall database
  5. ENDEDClass I · Most seriousRecalled Jul 2, 2021

    Blain's Farm & Fleet Select Dark Chocolate Amaretto Pecans, 12oz.

    Dark Chocolate Amaretto Pecans contain undeclared almonds.

    Eillien's Candies, Inc. · Green Bay, WI

    Where it was sold: Product was shipped to 1 distribution center located in Iowa.

    UPC 034952824971
    Show details
    Product, as FDA describes it
    Blain's Farm & Fleet Select Dark Chocolate Amaretto Pecans, 12oz.
    Reason, in FDA's words
    Dark Chocolate Amaretto Pecans contain undeclared almonds.
    Codes on the package
    Lot #: T04, Best By 04/29/22; UPC 034952824971
    Where it was sold
    Product was shipped to 1 distribution center located in Iowa.
    Amount recalled
    102 packages
    Status
    Ended Sep 3, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0845-2021
    View in FDA's recall database
  6. ENDEDClass II · ModerateRecalled Jun 29, 2021

    Pow Pow Powders: A standard of Quality Spice Chai; NET Wt. 3.50 lb. (1.59kg) Ingredients: Sugar, N...

    FDA inspection found that various smoothie mixes sold to restaurants did not include ingredient list or allergen information (undeclared milk)

    San Diego Coffee, Tea and Spice · Oceanside, CA

    Where it was sold: CA only.

    Show details
    Product, as FDA describes it
    Pow Pow Powders: A standard of Quality Spice Chai; NET Wt. 3.50 lb. (1.59kg) Ingredients: Sugar, Non-Dairy Creamer (coconut oil, Corn Syrup Solids, Sodium Caseinate (a milk derivative), Sodium Citrate, Mono and Diglycerides, Salt and sodium Aluminosilicate), Non-Fat Milk, Instant Black Tea, Dextrose, Honey, Natural and Artificial Flavors, Cinnamon, Carrageenan and Guar Gum
    Reason, in FDA's words
    FDA inspection found that various smoothie mixes sold to restaurants did not include ingredient list or allergen information (undeclared milk)
    Codes on the package
    90262/2141551
    Where it was sold
    CA only.
    Amount recalled
    75 bags - all flavors
    Status
    Ended Jul 28, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0782-2021
    View in FDA's recall database
  7. ENDEDClass II · ModerateRecalled Jun 29, 2021

    Pow Pow Powders: A standard of Quality Mocha Latte; NET Wt. 3.50 lb. (1.59kg) Ingredients: Sugar, ...

    FDA inspection found that various smoothie mixes sold to restaurants did not include ingredient list or allergen information (undeclared milk)

    San Diego Coffee, Tea and Spice · Oceanside, CA

    Where it was sold: CA only.

    Show details
    Product, as FDA describes it
    Pow Pow Powders: A standard of Quality Mocha Latte; NET Wt. 3.50 lb. (1.59kg) Ingredients: Sugar, Non-Dairy Creamer (coconut oil, Corn Syrup Solids, Sodium Caseinate (a milk derivative), Sodium Citrate, Mono and Diglycerides, Salt and sodium Aluminosilicate), Non-Fat Dry Milk, Cocoa Powder (dutched processed,Corn Syrup Solids, Instant Coffee, Silicon Dioxide (anti-caking agent), Vanillin, Natural and Artificial Flavor, Salt, Guar, Carrageenan and Xanthn Gum
    Reason, in FDA's words
    FDA inspection found that various smoothie mixes sold to restaurants did not include ingredient list or allergen information (undeclared milk)
    Codes on the package
    90263/2043572
    Where it was sold
    CA only.
    Amount recalled
    75 bags - all flavors
    Status
    Ended Jul 28, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0783-2021
    View in FDA's recall database
  8. ENDEDClass II · ModerateRecalled Jun 29, 2021

    Pow Pow Powders: A standard of Quality Vanilla Chai; NET Wt. 3.50 lb. (1.59kg) Ingredients: Sugar,...

    FDA inspection found that various smoothie mixes sold to restaurants did not include ingredient list or allergen information (undeclared milk)

    San Diego Coffee, Tea and Spice · Oceanside, CA

    Where it was sold: CA only.

    Show details
    Product, as FDA describes it
    Pow Pow Powders: A standard of Quality Vanilla Chai; NET Wt. 3.50 lb. (1.59kg) Ingredients: Sugar, Non-Fat Dry Milk, Non-Dairy Creamer (coconut oil, Corn Syrup Solids, Sodium Caseinate (a milk derivative), Sodium Citrate, Mono and Diglycerides, Salt), Instant Black Tea, Honey, Cinnamon, Natural and Artificial flavor. Carrageenan Gum, Silicon Dioxide (to prevent caking agent) and Guar Gum. Sodium Citrate, Mono and Diglyceride
    Reason, in FDA's words
    FDA inspection found that various smoothie mixes sold to restaurants did not include ingredient list or allergen information (undeclared milk)
    Codes on the package
    90262/2140971
    Where it was sold
    CA only.
    Amount recalled
    N/A
    Status
    Ended Jul 28, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0784-2021
    View in FDA's recall database
  9. ENDEDClass II · ModerateRecalled Jun 29, 2021

    Pow Pow Powders: A standard of Quality Hot Cocoa Mix; NET Wt. 3.50 lb. (1.59kg) Ingredients: Sugar...

    FDA inspection found that various smoothie mixes sold to restaurants did not include ingredient list or allergen information (undeclared milk)

    San Diego Coffee, Tea and Spice · Oceanside, CA

    Where it was sold: CA only.

    Show details
    Product, as FDA describes it
    Pow Pow Powders: A standard of Quality Hot Cocoa Mix; NET Wt. 3.50 lb. (1.59kg) Ingredients: Sugar, Non-Dairy Creamer (coconut oil, Corn Syrup Solids, Sodium Caseinate (a milk derivative), Sodium Citrate, Mono and Diglycerides, Salt), Cocoa (processed with alkali) Non-Fat Dry Milk, Corn Syrup Solids, Salt, Natural and Artificial flavor, Silicon Dioxide (to prevent caking agent) and Carrageenan.
    Reason, in FDA's words
    FDA inspection found that various smoothie mixes sold to restaurants did not include ingredient list or allergen information (undeclared milk)
    Codes on the package
    90265/2141552
    Where it was sold
    CA only.
    Amount recalled
    75 bags total - all flavors
    Status
    Ended Jul 28, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0785-2021
    View in FDA's recall database
  10. ENDEDClass II · ModerateRecalled Jun 24, 2021

    JERSEY COOKIE MONSTER ICE CREAM 3 GALLONS (11.34 LITERS) MFG: GREENWOOD ICE CREAM CO LTD 4829 PEA...

    During an FDA inspection the firm was notified that their ingredient statement does not include soy. Undeclared soy in ice cream

    Greenwood Ice Cream · Chamblee, GA

    Where it was sold: Product was shipped to the following states: AL, GA, NC, SC & TN.

    Show details
    Product, as FDA describes it
    JERSEY COOKIE MONSTER ICE CREAM 3 GALLONS (11.34 LITERS) MFG: GREENWOOD ICE CREAM CO LTD 4829 PEACHTREE ROAD, ATLANTA, GA 30341 UPC 0 12609 06378 0
    Reason, in FDA's words
    During an FDA inspection the firm was notified that their ingredient statement does not include soy. Undeclared soy in ice cream
    Codes on the package
    Lot Numbers: 22168, 22163, 2155, 22149, 22140, 22139, 22133, 22126, 22119, 22113, 22108, 22098, 22091, 22087, 22080, 22079, 22077, 22069, 22057, 22045, 22036, 22029, 22016, 22015, 21353, 21338, 21323, 21310, 21296, 21289, 21281, 21269, 21268, 21267, 21261, 21260, 21246, 21241, 21228, 21224, 21217, 21211, 21198, 21197, 21189, 21182, 21175, 21168, 21161, 21154.
    Where it was sold
    Product was shipped to the following states: AL, GA, NC, SC & TN.
    Amount recalled
    2,454/3 gallon tubs
    Status
    Ended (FDA lists it as completed)
    FDA recall number
    F-0768-2021
    View in FDA's recall database
  11. ENDEDClass I · Most seriousRecalled Jun 23, 2021

    Hartley's brand Worcestershire sauce in 1 gallon plastic bottles and 50 gallon drums.

    Undeclared allergen: FISH (anchovies) on product labeling.

    H & H Products Company · Orlando, FL

    Where it was sold: Product was sold to distributors in FL, AL, GA in 1 gallon and 50 gallon drums.

    Show details
    Product, as FDA describes it
    Hartley's brand Worcestershire sauce in 1 gallon plastic bottles and 50 gallon drums.
    Reason, in FDA's words
    Undeclared allergen: FISH (anchovies) on product labeling.
    Codes on the package
    Lot numbers: HH21-138; HH20-349; HH21-053; HH21-113; HH21-067; HH21-131; HH210-113
    Where it was sold
    Product was sold to distributors in FL, AL, GA in 1 gallon and 50 gallon drums.
    Amount recalled
    1 gallon bottles: 3,184; 50 gallon drums: 16
    Status
    Ended Feb 3, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0762-2021
    View in FDA's recall database
  12. ENDEDClass II · ModerateRecalled Jun 22, 2021

    Milo's Sauce 5 gallon pails 24 pails per pallet

    Undeclared Fish Allergen

    Southern Classic Food Group LLC · 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
    View in FDA's recall database
  13. ENDEDClass II · 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 · 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
    View in FDA's recall database
  14. ENDEDClass II · 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 · 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
    View in FDA's recall database
  15. ENDEDClass II · 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 · 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
    View in FDA's recall database
  16. ENDEDClass II · 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 · 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
    View in FDA's recall database
  17. ENDEDClass II · 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 · 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
    View in FDA's recall database
  18. ENDEDClass II · 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 · 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
    View in FDA's recall database
  19. ENDEDClass II · 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 · 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
    View in FDA's recall database
  20. ENDEDClass II · 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 · 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
    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.