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FDA FOOD RECALLS

Look up any food recall

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

610 recalls · showing 241 to 260

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  1. ENDEDClass I · Most seriousRecalled Aug 2, 2021

    Golden Natural Product Inc. brand Dried Apricot Subkhon with Bone, Net Wt. 16 oz (1 lb) 454 g; and G...

    Product contains high levels of undeclared sulfites.

    Golden Natural Products · Brooklyn, NY

    Where it was sold: NY, CA, WA

    Show details
    Product, as FDA describes it
    Golden Natural Product Inc. brand Dried Apricot Subkhon with Bone, Net Wt. 16 oz (1 lb) 454 g; and Golden Natural Product Inc. brand Dried Apricot Subkhon Jumbo, Net Wt. 16 oz (1 lb) 454 g Manufactured and Packed by: Gardencells LLC, Urgut, Samarkand region Republic of Uzbekistan; Distributed in USA by: GOLDEN NATURAL PRODUCTS INC.
    Reason, in FDA's words
    Product contains high levels of undeclared sulfites.
    Codes on the package
    Lot: GC005 Exp: 2023
    Where it was sold
    NY, CA, WA
    Amount recalled
    Unknown
    Status
    Ended Dec 8, 2023 (FDA lists it as terminated)
    FDA recall number
    F-1006-2021
    View in FDA's recall database
  2. ENDEDClass I · Most seriousRecalled Jul 16, 2021

    Backcountry Dried Apricots 9ounce plastic bag 12 packages per case

    Sulfites not disclosed on labeling

    Lipari Foods Operating Company, LLC. · Warren, MI

    Where it was sold: Distributed to retail locations in the following states: AL, FL, GA, ID, IL, IN, KS, KY, MI, MO, NC, OH, PA, TN, UT, VA, WI WV.

    Show details
    Product, as FDA describes it
    Backcountry Dried Apricots 9ounce plastic bag 12 packages per case
    Reason, in FDA's words
    Sulfites not disclosed on labeling
    Codes on the package
    Best By Dates: 07/2021, 11/2021, 12/2021 Lot No. 440021117 Product No. 276033
    Where it was sold
    Distributed to retail locations in the following states: AL, FL, GA, ID, IL, IN, KS, KY, MI, MO, NC, OH, PA, TN, UT, VA, WI WV.
    Amount recalled
    86 cases
    Status
    Ended Sep 23, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0795-2021
    View in FDA's recall database
  3. ENDEDClass II · ModerateRecalled Jul 1, 2021

    Vegetable egg rolls packaged either 96 3oz per case or 120 2oz per case, Manufacturer T&R Enterprise...

    Products contain Yellow #5 but it is not declared on the label

    T & R Enterprises USA, Inc. · Saint Louis, MO

    Where it was sold: Distributed to restaurants in the St. Louis, MO area.

    Show details
    Product, as FDA describes it
    Vegetable egg rolls packaged either 96 3oz per case or 120 2oz per case, Manufacturer T&R Enterprises St. Louis MO.
    Reason, in FDA's words
    Products contain Yellow #5 but it is not declared on the label
    Codes on the package
    Best by October 2021 and earlier.
    Where it was sold
    Distributed to restaurants in the St. Louis, MO area.
    Amount recalled
    630 cases
    Status
    Ended Nov 4, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0868-2021
    View in FDA's recall database
  4. ACTIVEClass II · ModerateRecalled May 12, 2021

    Lipodrene With 25mg Ephedra Extract 100CT UPC 8 57084 00056 9

    The firm was notified by the FDA that the product contains the unapproved food additive 1,4-dimethylamylamine (DMAA).

    Hi Tech Pharmaceuticals · Norcross, GA

    Where it was sold: The product was shipped to the following states: AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, ME, MI, MO, MS, MT, NC, NE, NE, NJ, NM, NV, NY, OH, OK, OR, PA, PR, TN,...

    UPC 857084000569
    Show details
    Product, as FDA describes it
    Lipodrene With 25mg Ephedra Extract 100CT UPC 8 57084 00056 9
    Reason, in FDA's words
    The firm was notified by the FDA that the product contains the unapproved food additive 1,4-dimethylamylamine (DMAA).
    Codes on the package
    Lot # 001211197, Exp. 12/25
    Where it was sold
    The product was shipped to the following states: AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, ME, MI, MO, MS, MT, NC, NE, NE, NJ, NM, NV, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, VT, WA & WI.
    Amount recalled
    19,068/100 ct bottles
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    F-0647-2021
    View in FDA's recall database
  5. ENDEDClass II · ModerateRecalled Apr 27, 2021

    White Oak Farm & Table brand Pear Gorgonzola Salad Dressing & Dipping Sauce; 12 Fl OZ, packaged in g...

    Product contains undeclared Dijon mustard and red wine vinegar, which resulted in naturally occurring sulfites being undeclared on the label.

    Global Palate Foods · Bridgeport, CT

    Where it was sold: NY, NH, CT

    Show details
    Product, as FDA describes it
    White Oak Farm & Table brand Pear Gorgonzola Salad Dressing & Dipping Sauce; 12 Fl OZ, packaged in glass bottles
    Reason, in FDA's words
    Product contains undeclared Dijon mustard and red wine vinegar, which resulted in naturally occurring sulfites being undeclared on the label.
    Codes on the package
    Lot #'s: 100621, 121221, 012322, 021722, 0421222, 070722, 081122, 091823
    Where it was sold
    NY, NH, CT
    Amount recalled
    1,693 cases
    Status
    Ended Jan 13, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0496-2021
    View in FDA's recall database
  6. ENDEDClass II · ModerateRecalled Apr 8, 2021

    J-Basket Premium Korean Seaweed Snack - Wasabi flavor on outer wrap for 3 inner packages Inner packa...

    Wasabi Flavor Seaweed snack is incorrectly packaged in Original Seaweed Flavor package which does not declare FD&C Yellow 5 and FD&C Blue No 1.

    J F C International Inc · Commerce, CA

    Where it was sold: CA, WA, AZ, TX, LA, AR, KY, NE, WI, IL, MO, IA, OH, MI.

    UPC 011152295077
    Show details
    Product, as FDA describes it
    J-Basket Premium Korean Seaweed Snack - Wasabi flavor on outer wrap for 3 inner packages Inner packages labeled J-Basket Premium Seaweed Snack - Original. Net Wt 0.52 oz. (15g) 3-0.17 oz. (5g) packs Distributed by JFC International Inc., Los Angeles, CA 90040 Wasabi outer package UPC 0 11152 29507 7 Ingredients: Wasabi: Seaweed, corn oil, sesame oil, wasabi powder (mustard {Ally Isothiocyante, Maltodextrin, arabic gum, palm oil, rosemary oleoresini}, dextrin, wasabi, FD&C Yellow #5, FD&C Blue No 1. Ingredients Original: Seaweed, Corn oil, Sesame oil, Salt.
    Reason, in FDA's words
    Wasabi Flavor Seaweed snack is incorrectly packaged in Original Seaweed Flavor package which does not declare FD&C Yellow 5 and FD&C Blue No 1.
    Codes on the package
    Best Before: 01.03.2022 / 01.10.2022, JFC Item#29507
    Where it was sold
    CA, WA, AZ, TX, LA, AR, KY, NE, WI, IL, MO, IA, OH, MI.
    Amount recalled
    451 boxes
    Status
    Ended May 24, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0429-2021
    View in FDA's recall database
  7. ENDEDClass II · ModerateRecalled Mar 30, 2021

    Motha Jelly Crystals - Mixed Fruit Flavoured Jelly, Net Wt. 100g,

    Jelly contains undeclared FD&C yellow #5 and blue #1, and unapproved carmoisine (E122)/dye 14720/acid red 14

    USA LANKA INC · Elmont, NY

    Where it was sold: NY, MA, MD, CT, CA, PA, MS, NC, NJ, TX

    UPC 4792551000405
    Show details
    Product, as FDA describes it
    Motha Jelly Crystals - Mixed Fruit Flavoured Jelly, Net Wt. 100g,
    Reason, in FDA's words
    Jelly contains undeclared FD&C yellow #5 and blue #1, and unapproved carmoisine (E122)/dye 14720/acid red 14
    Codes on the package
    EXP: 08/15/2022, BATCH#: C0818 B; UPC#: 4792551000405
    Where it was sold
    NY, MA, MD, CT, CA, PA, MS, NC, NJ, TX
    Amount recalled
    271 units
    Status
    Ended May 18, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0446-2021
    View in FDA's recall database
  8. ENDEDClass II · ModerateRecalled Mar 30, 2021

    Motha Jelly Crystals - Black Currant Flavoured Jelly, Net Wt. 100g

    Jelly contain undeclared FD&C yellow #5 and blue #1, and unapproved carmoisine (E122)/dye 14720/acid red 14

    USA LANKA INC · Elmont, NY

    Where it was sold: NY, MA, MD, CT, CA, PA, MS, NC, NJ, TX

    UPC 4792551000047
    Show details
    Product, as FDA describes it
    Motha Jelly Crystals - Black Currant Flavoured Jelly, Net Wt. 100g
    Reason, in FDA's words
    Jelly contain undeclared FD&C yellow #5 and blue #1, and unapproved carmoisine (E122)/dye 14720/acid red 14
    Codes on the package
    EXP: 02/18/2022, BATCH#: C0219 A; UPC#: 4792551000047
    Where it was sold
    NY, MA, MD, CT, CA, PA, MS, NC, NJ, TX
    Amount recalled
    268 units
    Status
    Ended May 18, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0447-2021
    View in FDA's recall database
  9. ENDEDClass II · ModerateRecalled Mar 30, 2021

    Motha Jelly Crystals - Mango Flavoured Jelly, Net Wt. 100g

    Jelly contains undeclared FD&C Yellow #5 and FD&C Yellow #6

    USA LANKA INC · Elmont, NY

    Where it was sold: NY, MA, MD, CT, CA, PA, MS, NC, NJ, TX

    UPC 4792551000344
    Show details
    Product, as FDA describes it
    Motha Jelly Crystals - Mango Flavoured Jelly, Net Wt. 100g
    Reason, in FDA's words
    Jelly contains undeclared FD&C Yellow #5 and FD&C Yellow #6
    Codes on the package
    EXP: 05/22/2022, UPC#: 4792551000344, BATCH#: C0523
    Where it was sold
    NY, MA, MD, CT, CA, PA, MS, NC, NJ, TX
    Amount recalled
    557 units
    Status
    Ended May 18, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0448-2021
    View in FDA's recall database
  10. ENDEDClass III · Low riskRecalled Mar 30, 2021

    Motha Jelly Crystals Strawberry Flavoured Jelly , Net Wt. 100g

    Jelly contains undeclared FD&C Red #40

    USA LANKA INC · Elmont, NY

    Where it was sold: NY, MA, MD, CT, CA, PA, MS, NC, NJ, TX

    UPC 4792551000016
    Show details
    Product, as FDA describes it
    Motha Jelly Crystals Strawberry Flavoured Jelly , Net Wt. 100g
    Reason, in FDA's words
    Jelly contains undeclared FD&C Red #40
    Codes on the package
    EXP: 08/15/2022, UPC#: 4792551000016, BATCH#: C0825 B
    Where it was sold
    NY, MA, MD, CT, CA, PA, MS, NC, NJ, TX
    Amount recalled
    577 units
    Status
    Ended May 18, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0449-2021
    View in FDA's recall database
  11. ENDEDClass II · ModerateRecalled Mar 30, 2021

    Motha Jelly Crystals - Orange Flavoured Jelly, Net Wt. 100g

    Jelly contains undeclared FD&C Yellow #6

    USA LANKA INC · Elmont, NY

    Where it was sold: NY, MA, MD, CT, CA, PA, MS, NC, NJ, TX

    UPC 4792551000313
    Show details
    Product, as FDA describes it
    Motha Jelly Crystals - Orange Flavoured Jelly, Net Wt. 100g
    Reason, in FDA's words
    Jelly contains undeclared FD&C Yellow #6
    Codes on the package
    EXP: 05/18/2022, UPC#: 4792551000313, BATCH#: C0519
    Where it was sold
    NY, MA, MD, CT, CA, PA, MS, NC, NJ, TX
    Amount recalled
    433 units
    Status
    Ended May 18, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0450-2021
    View in FDA's recall database
  12. ENDEDClass II · ModerateRecalled Mar 18, 2021

    Anand Far Far (Garlic Sandige) Net Weight 7 oz./200 g package ingredients: rice, wheat flour, garl...

    The product was found to contain undeclared yellow# 6, verified via private lab analysis.

    Babco Foods International, LLC · Hayward, CA

    Where it was sold: AZ, CA,WA.

    UPC 878776002326
    Show details
    Product, as FDA describes it
    Anand Far Far (Garlic Sandige) Net Weight 7 oz./200 g package ingredients: rice, wheat flour, garlic, red chilli, refined palm oil and salt. UPC 8 78776 00232 6 Product of India Imported and Distributed by Babco Foods International, LLC, Bridgewater, NJ
    Reason, in FDA's words
    The product was found to contain undeclared yellow# 6, verified via private lab analysis.
    Codes on the package
    Batch DD 20, Best Before Oct 2021.
    Where it was sold
    AZ, CA,WA.
    Amount recalled
    10 cases
    Status
    Ended Apr 12, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0424-2021
    View in FDA's recall database
  13. ENDEDClass III · Low riskRecalled Feb 26, 2021

    Electrolit Ponche/Fruit Punch; in 625 mL/21 oz and 300ML/10oz bottles; and Electrolit Fruit Punch 6 ...

    Product contains undeclared FD&C Red No. 40.

    Laboratorios Pisa Sa De Cv · Guadalajara, N/A

    Where it was sold: OK, CA, WI, TX, IN, IA, NV, FL, NC, IL, KY, OH, NY, PA, AZ, MO, AL, VA, CO, WA, MN, GA,

    Show details
    Product, as FDA describes it
    Electrolit Ponche/Fruit Punch; in 625 mL/21 oz and 300ML/10oz bottles; and Electrolit Fruit Punch 6 Pack, 625mL/21 oz; Packaged in a polypropylene bottle with volume capacity 625 mL and a polypropylene lid and liner with a high-density polyethylene safety ring.
    Reason, in FDA's words
    Product contains undeclared FD&C Red No. 40.
    Codes on the package
    625mL/21oz: Lot #'s: M20D310; M20D311; M20D312; M20D320; M20D327; M20D328; M20D348; M20E306; M20E361; M20E362; M20E363; M20E364; M20F357; M20J308; M20J309; M20J310; M20J311; M20M314; M20M317; M20Y362; M20Y363; M20D324; M20D326; M20D330; M20E305; M20J305; M20J312; M20Y364; M20Y365; M20Y366; M20U341 625mL/21oz Exp. Dates: 2023-12; 2023-12; 2023-12; 2023-12; 2023-12; 2023-12; 2023-12; 2023-01; 2023-01; 2023-01; 2023-01; 2023-01; 2023-02; 2023-06; 2023-06; 2023-06; 2023-06; 2023-03; 2023-03; 2023-05; 2023-05; 2023-12; 2023-12; 2023-12; 2023-01; 2023-06; 2023-06; 2023-05; 2023-05; 2023-05; 2023-07 300ML/10OZ Lot #'s: H20Y324; H20M130; H20Y328; H20Y361 300ML/10OZ Exp Dates: 2023-05; 2023-03; 2023-05; 2023-05 6 Pack - 625mL/21 oz Lot #'s: M20J304; M20M316 6 Pack - 625mL/21 oz Exp Dates: 2023-06; 2023-03
    Where it was sold
    OK, CA, WI, TX, IN, IA, NV, FL, NC, IL, KY, OH, NY, PA, AZ, MO, AL, VA, CO, WA, MN, GA,
    Amount recalled
    571,590 bottles
    Status
    Ended Oct 1, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0363-2021
    View in FDA's recall database
  14. ENDEDClass III · Low riskRecalled Feb 26, 2021

    Electrolit Fruit Punch Zero, 625ML/21OZ packaged in a polypropylene bottle with volume capacity of 6...

    Product contains undeclared FD&C Red No. 40.

    Laboratorios Pisa Sa De Cv · Guadalajara, N/A

    Where it was sold: OK, CA, WI, TX, IN, IA, NV, FL, NC, IL, KY, OH, NY, PA, AZ, MO, AL, VA, CO, WA, MN, GA,

    Show details
    Product, as FDA describes it
    Electrolit Fruit Punch Zero, 625ML/21OZ packaged in a polypropylene bottle with volume capacity of 625mL and with a polypropylene lid and liner with a high-density polyethylene safety ring.
    Reason, in FDA's words
    Product contains undeclared FD&C Red No. 40.
    Codes on the package
    Lot #'s: M21E366; M21E367 Exp. Dates: 2024-01; 2024-01
    Where it was sold
    OK, CA, WI, TX, IN, IA, NV, FL, NC, IL, KY, OH, NY, PA, AZ, MO, AL, VA, CO, WA, MN, GA,
    Amount recalled
    571,590 bottles
    Status
    Ended Oct 1, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0364-2021
    View in FDA's recall database
  15. ENDEDClass III · Low riskRecalled Feb 19, 2021

    YUM CRUMBS, STRAWBERRY SHORTCAKE, 12 oz and 32 oz

    Undeclared Red #40

    THE SAPPHIRE EXCHANGE · Edgewater, FL

    Sold in the U.S. (states not listed)

    Where it was sold: Domestic distribution only

    Show details
    Product, as FDA describes it
    YUM CRUMBS, STRAWBERRY SHORTCAKE, 12 oz and 32 oz
    Reason, in FDA's words
    Undeclared Red #40
    Codes on the package
    Not listed
    Where it was sold
    Domestic distribution only
    Amount recalled
    3,421 bottles
    Status
    Ended Aug 2, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0333-2021
    View in FDA's recall database
  16. ENDEDClass III · Low riskRecalled Feb 18, 2021

    Ferrara Candy Company assorted candy Heart Box, including Laffy Taffy, Nerds, and SweeTarts candies....

    Undeclared ingredients on retail packaging, including but not limited to certified colors Red #40 and Blue #1

    Ferrara Candy Company · Chicago, IL

    Where it was sold: Nationwide retail

    UPC 041420049651
    Show details
    Product, as FDA describes it
    Ferrara Candy Company assorted candy Heart Box, including Laffy Taffy, Nerds, and SweeTarts candies. 10 retail units per wholesale case. Package UPC 0 41420 04965 1
    Reason, in FDA's words
    Undeclared ingredients on retail packaging, including but not limited to certified colors Red #40 and Blue #1
    Codes on the package
    All product distributed prior to 2/18/2021
    Where it was sold
    Nationwide retail
    Amount recalled
    3832 cases
    Status
    Ended Sep 1, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0336-2021
    View in FDA's recall database
  17. ACTIVEClass II · ModerateRecalled Nov 17, 2020

    PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY and IMMUNE HEALTH Dietary Supplement 30 ...

    The firm is recalling their products due the unapproved use of a food additive and unapproved marketing statements

    Fusion Health and Vitality LLC · Alpharetta, GA

    Where it was sold: Product was shipped nationwide to all 50 states

    UPC 728028210545
    Show details
    Product, as FDA describes it
    PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY and IMMUNE HEALTH Dietary Supplement 30 Servings (45g) Supplement Facts***Hordenine HCL*** Manufactured by: Fusion Health Vitality, LLC 1360 Union Hill Road, Suite 11B Alpharetta, GA 30004 888.964.5327 UPC 7 28028 21054 5
    Reason, in FDA's words
    The firm is recalling their products due the unapproved use of a food additive and unapproved marketing statements
    Codes on the package
    Lot # s: 200313, 200321, 200326, 200402, 200406, 200410, 200414, 200416, 200424, 200501, 200525, 200527, 200604 & 200610.
    Where it was sold
    Product was shipped nationwide to all 50 states
    Amount recalled
    10,000/45g jars
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    F-0180-2021
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled Nov 6, 2020

    Green Raisins 200 grams (7 oz.) Packaged in plastic bags. Bar Code:992203621

    Undeclared sulfites

    Singh Trading Inc. DBA Roshni Foods · Laurel, MD

    Where it was sold: This product is distributed to retail stores in NC, MD, VA, and PA

    Show details
    Product, as FDA describes it
    Green Raisins 200 grams (7 oz.) Packaged in plastic bags. Bar Code:992203621
    Reason, in FDA's words
    Undeclared sulfites
    Codes on the package
    Batch 20020
    Where it was sold
    This product is distributed to retail stores in NC, MD, VA, and PA
    Amount recalled
    20 cases
    Status
    Ended Jan 13, 2022 (FDA lists it as terminated)
    FDA recall number
    F-0125-2021
    View in FDA's recall database
  19. ENDEDClass I · Most seriousRecalled Apr 22, 2020

    TAINY BOCTOKA DRY FRUITS MIX COMPOT APPLE; Assorted dried fruits; NET WT 17.63 oz (500g) clear plast...

    Product contains undeclared sulfites.

    Royal International Trading Inc. · Brooklyn, NY

    Where it was sold: MA, CT, NJ, VA, FL, MN, IL, PA, NY, OH, IN

    Show details
    Product, as FDA describes it
    TAINY BOCTOKA DRY FRUITS MIX COMPOT APPLE; Assorted dried fruits; NET WT 17.63 oz (500g) clear plastic package
    Reason, in FDA's words
    Product contains undeclared sulfites.
    Codes on the package
    Container code 4705932006197
    Where it was sold
    MA, CT, NJ, VA, FL, MN, IL, PA, NY, OH, IN
    Amount recalled
    30 cases
    Status
    Ended Apr 29, 2021 (FDA lists it as terminated)
    FDA recall number
    F-0937-2020
    View in FDA's recall database
  20. ENDEDClass II · ModerateRecalled Apr 20, 2020

    5.5 oz cans of Ocean Spray Pink Lite Cranberry Juice Drink

    Product contains undeclared sulfites.

    Ocean Spray Cranberries Inc. · Lakeville, MA

    Where it was sold: AL, AZ, CA, CO, CT, GA, IA, IL, IN, KS, LA, MA, MI, MN, MO, NC, NI, NJ, NY, OK, OR, PA, SC, TX, VA, WA, WI

    UPC 031200037824UPC 031200236821
    Show details
    Product, as FDA describes it
    5.5 oz cans of Ocean Spray Pink Lite Cranberry Juice Drink
    Reason, in FDA's words
    Product contains undeclared sulfites.
    Codes on the package
    Best Before 24Jan21 Pack Case UPC: 03120003782 4 Can UPC: 0003120023682 1 GTIN Case:003120023682 1 GTIN Case: 003120024682 0
    Where it was sold
    AL, AZ, CA, CO, CT, GA, IA, IL, IN, KS, LA, MA, MI, MN, MO, NC, NI, NJ, NY, OK, OR, PA, SC, TX, VA, WA, WI
    Amount recalled
    206,106 cans
    Status
    Ended Sep 10, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0927-2020
    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.