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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

7,651 recalls · showing 2,301 to 2,320

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  1. ENDEDClass II · ModerateRecalled Aug 10, 2021

    Wegmans Sunflower Crunch Chopped Salad Kit: Includes Green Cabbage, Green Leaf Lettuce, Sunflower Se...

    Undeclared allergens in salad mix - milk and wheat. Cheese and croutons are packed separately and clearly visible to consumer.

    Taylor Farms Retail, Inc. · Salinas, CA

    Where it was sold: Two DC's in NY and PA

    UPC 077890502389
    Show details
    Product, as FDA describes it
    Wegmans Sunflower Crunch Chopped Salad Kit: Includes Green Cabbage, Green Leaf Lettuce, Sunflower Seeds, Red Cabbage, Carrot, Kale, Uncured Bacon, Green Onion with Wegmans Organic Coleslaw dressing. Washed and ready to eat. Salad and toppings: Net Wt 10.1 oz. (286 g) Dressing: Net 2.58 Fl Oz. (76 mL) Total Net Wt 12.6 oz. (357 g) UPC: 0 77890 50238 9. Distributed by Wegmans Markets Inc., Rochester, NY 14603 Allergens: Contains Eggs
    Reason, in FDA's words
    Undeclared allergens in salad mix - milk and wheat. Cheese and croutons are packed separately and clearly visible to consumer.
    Codes on the package
    BEST If Used By 8/11/2021
    Where it was sold
    Two DC's in NY and PA
    Amount recalled
    111 cases (999 units)
    Status
    Ended Aug 23, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0877-2021
    View in FDA's recall database
  2. ENDEDClass I · Most seriousRecalled Aug 9, 2021

    Marketside Chocolate Candy Cookie Cake, 24 oz. 12 x 12 black tray with clear lid.

    Undeclared allergen - Peanuts.

    Jimmy's Cookies, LLC · Clifton, NJ

    Where it was sold: The recalled product was distributed to the following States: AR, FL, OK, IL, Al, LA, OH, TX, KY, OH, MS, WI, IN, TN .

    Show details
    Product, as FDA describes it
    Marketside Chocolate Candy Cookie Cake, 24 oz. 12 x 12 black tray with clear lid.
    Reason, in FDA's words
    Undeclared allergen - Peanuts.
    Codes on the package
    Lot# 1133
    Where it was sold
    The recalled product was distributed to the following States: AR, FL, OK, IL, Al, LA, OH, TX, KY, OH, MS, WI, IN, TN .
    Amount recalled
    2592 Cases
    Status
    Ended Jan 7, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0961-2021
    View in FDA's recall database
  3. ENDEDClass II · ModerateRecalled Aug 7, 2021

    Flourless Chocolate Torte, 14 oz., in recyclable plastic circular container with black base and clea...

    Frozen desserts are mislabeled. Flourless Chocolate Torte mislabeled with Triple Berry Streusel Cheesecake ingredients and nutrition label. Chocolate ...

    Gem City Fine Foods, LLC · West Valley City, UT

    Where it was sold: Two distributors in CO, TX.

    UPC 855026001186
    Show details
    Product, as FDA describes it
    Flourless Chocolate Torte, 14 oz., in recyclable plastic circular container with black base and clear lid, Gem City Fine Foods, 3403 S 1400 W, Suite C, West Valley City, UT 84119. There are 4/cs. UPC 855026001186. Store Frozen or Thawed in Fridge.
    Reason, in FDA's words
    Frozen desserts are mislabeled. Flourless Chocolate Torte mislabeled with Triple Berry Streusel Cheesecake ingredients and nutrition label. Chocolate Torte and Triple Berry Streusel are both mislabeled with pecans as an ingredient although firm has not used nuts of any kind in its products or the facility since April 2018.
    Codes on the package
    Batch 21181-06; Best by June 30, 2022
    Where it was sold
    Two distributors in CO, TX.
    Amount recalled
    51 cases of 4/case
    Status
    Ended Jul 14, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0928-2021
    View in FDA's recall database
  4. ENDEDClass III · Low riskRecalled Aug 7, 2021

    Triple Berry Streusel Cheesecake, 20 oz., in recyclable plastic circular container with black base a...

    Frozen desserts are mislabeled. Flourless Chocolate Torte mislabeled with Triple Berry Streusel Cheesecake ingredients and nutrition label. Chocolate ...

    Gem City Fine Foods, LLC · West Valley City, UT

    Where it was sold: Two distributors in CO, TX.

    UPC 855026001193
    Show details
    Product, as FDA describes it
    Triple Berry Streusel Cheesecake, 20 oz., in recyclable plastic circular container with black base and clear lid, Gem City Fine Foods, 3403 S 1400 W, Suite C, West Valley City, UT 84119. There are 4/cs. UPC 855026001193. Store Frozen or Thawed in Fridge.
    Reason, in FDA's words
    Frozen desserts are mislabeled. Flourless Chocolate Torte mislabeled with Triple Berry Streusel Cheesecake ingredients and nutrition label. Chocolate Torte and Triple Berry Streusel are both mislabeled with pecans as an ingredient although firm has not used nuts of any kind in its products or the facility since April 2018.
    Codes on the package
    Batch 21168-04; Best by June 17, 2022 Batch 21187-06; Best by July 6, 2022 Batch 21188-06; Best by July 7, 2022 Batch 21179-05; Best by June 28, 2022
    Where it was sold
    Two distributors in CO, TX.
    Amount recalled
    196 cases
    Status
    Ended Jul 14, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0929-2021
    View in FDA's recall database
  5. ENDEDClass II · ModerateRecalled Aug 6, 2021

    Fermentation Derived Pepsin Product packaging: 5 individual LDPE bags with a net weight of 5kg each...

    Undeclared egg allergen

    Ingredion · Bridgewater, NJ

    Where it was sold: Distributed in the following states: CA, MA, FL, WA, UT, TX, ID, CT, IL, and SC.

    Show details
    Product, as FDA describes it
    Fermentation Derived Pepsin Product packaging: 5 individual LDPE bags with a net weight of 5kg each and 2.5kg sample bags packaged in 25 kg HDPE Drums
    Reason, in FDA's words
    Undeclared egg allergen
    Codes on the package
    20352B1 20352B2 21054B1 21054B2 21078B Sample 20223B1 Sample 20223B2 Sample PRTN02000510KFP093B Sample 20101114F14FB15F2F Sample 0201011114F14FB Sample PRTN02000610KFP093B Sample 021B023KFP
    Where it was sold
    Distributed in the following states: CA, MA, FL, WA, UT, TX, ID, CT, IL, and SC.
    Amount recalled
    370 kg s
    Status
    Ended Jun 10, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0956-2021
    View in FDA's recall database
  6. ACTIVEClass II · ModerateRecalled Aug 4, 2021

    MOLLY & ME PECANS all natural PRALINE PECANS, 4 oz., 7 oz., and 12 oz packages, INGREDIENTS: Pecans,...

    The firm was notified during an inspection by the State that the product contains undeclared soy.

    Molly and Me Pecans · Holly Hill, SC

    Where it was sold: The product was shipped to the following states: AL, AR, AZ, CA, CO, FL, GA, IL, IN, KS, KY, MA, MD, MI, MN, NC, NE, NJ, NV, NY, OH, PA, SC, TN, TX, VA, VT & WV. Product was als...

    Show details
    Product, as FDA describes it
    MOLLY & ME PECANS all natural PRALINE PECANS, 4 oz., 7 oz., and 12 oz packages, INGREDIENTS: Pecans, Brown Sugar, Evaporated Milk, Margarine, Light Corn syrup, Artificial Vanilla Flavor. ALLERGEN INFORMATION CONTAINS MILK, PECANS & MAY CONTAIN OTHER TREE NUTS. PRODUCED & DISTRIBUTED BY: MOLLY & ME PECANS LLC 9008 OLD STATE RD. HOLLY HILL, SC 29059
    Reason, in FDA's words
    The firm was notified during an inspection by the State that the product contains undeclared soy.
    Codes on the package
    All date codes
    Where it was sold
    The product was shipped to the following states: AL, AR, AZ, CA, CO, FL, GA, IL, IN, KS, KY, MA, MD, MI, MN, NC, NE, NJ, NV, NY, OH, PA, SC, TN, TX, VA, VT & WV. Product was also shipped to the United Kingdom
    Amount recalled
    1,221/4oz packages; 346/7oz packages & 10/12oz packages
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    F-0858-2021
    View in FDA's recall database
  7. ENDEDClass I · Most seriousRecalled Aug 4, 2021

    Dark Chocolate Malt Balls in plastic container; 9 oz./ 255g UPC: 6 5143370179 0 Packed on the sam...

    Firm notified by customers that product labeled as Dark Chocolate Malt Balls had Dark Chocolate Peanut Butter malt balls inside - undeclared peanuts.

    DSD Merchandisers, Inc. · Livermore, CA

    Where it was sold: CA, HI

    UPC 651433701790
    Show details
    Product, as FDA describes it
    Dark Chocolate Malt Balls in plastic container; 9 oz./ 255g UPC: 6 5143370179 0 Packed on the same equipment as products that contain milk, eggs, tree nuts, peanuts, wheat and soy. Distributed by DSD Merchandisers, Inc., Livermore, CA 64551
    Reason, in FDA's words
    Firm notified by customers that product labeled as Dark Chocolate Malt Balls had Dark Chocolate Peanut Butter malt balls inside - undeclared peanuts.
    Codes on the package
    Best Before 3/1/2022
    Where it was sold
    CA, HI
    Amount recalled
    252 units
    Status
    Ended Sep 3, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0871-2021
    View in FDA's recall database
  8. ENDEDClass II · ModerateRecalled Aug 3, 2021

    Moonwalk 70% dark chocolate bar. It is packaged in white shiny paper with blue print. Net Weight: ...

    Lactose is declared but milk is not declared on label.

    Cocanu LLC · Portland, OR

    Where it was sold: Distributed in CA and OR.

    Show details
    Product, as FDA describes it
    Moonwalk 70% dark chocolate bar. It is packaged in white shiny paper with blue print. Net Weight: 1.2 oz / 35gr. No UPC. The label is read in parts: "***Moonwalk ***a 70% dark chocolate bar ***chocolate, cacao nibs and pop rocks ***Contents: cacao beans, cacao butter, cane sugar, pop rocks (sugar, lactose, corn syrup, flavoring)***cloudforest Portland, OR***cloudforest.shop***".
    Reason, in FDA's words
    Lactose is declared but milk is not declared on label.
    Codes on the package
    Lot 683 (Best by 8/26/2021) Lot 690 (Best by 12/15/2021) Lot 695 (Best by 12/30/2021) Lot 703 (Best by 2/11/2022) Lot 709 (Best by 3/10/2022) Lot 722 (Best by 5/28/2022)
    Where it was sold
    Distributed in CA and OR.
    Amount recalled
    852 bars
    Status
    Ended May 13, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0867-2021
    View in FDA's recall database
  9. ENDEDClass II · ModerateRecalled Jul 27, 2021

    Grab & Go Bistro Pimento Cheese Sandwich 5oz plastic container 1 sandwich per package

    Fish not declared as an allergen

    Modern Distributors, Inc. dba Modern Vending · Somerset, KY

    Where it was sold: Distributed to firm owned vending machines within Kentucky

    Show details
    Product, as FDA describes it
    Grab & Go Bistro Pimento Cheese Sandwich 5oz plastic container 1 sandwich per package
    Reason, in FDA's words
    Fish not declared as an allergen
    Codes on the package
    UPC 000000999281 ID 99928
    Where it was sold
    Distributed to firm owned vending machines within Kentucky
    Amount recalled
    43 units
    Status
    Ended Oct 1, 2021 (FDA lists it as terminated)
    FDA recall number
    F-1026-2021
    View in FDA's recall database
  10. 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
  11. 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
  12. 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
  13. 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
  14. 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
  15. 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
  16. 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
  17. 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
  18. 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
  19. 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
  20. 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

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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.