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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 5,101 to 5,120

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  1. ENDEDClass II · ModerateRecalled Mar 15, 2016

    Nuwati Herbals SeeLessO'Me Diet and Weight Management Tea packaged in two different size amber glass...

    Product contains undeclared soy.

    Nuwati Herbals Inc · Saint Charles, MO

    Where it was sold: Nationwide.

    Show details
    Product, as FDA describes it
    Nuwati Herbals SeeLessO'Me Diet and Weight Management Tea packaged in two different size amber glass jars with Net Wt 3 oz. or Net Wt 6 oz. The responsible name on the label is Nuwati Herbals Inc., House Springs, MO.
    Reason, in FDA's words
    Product contains undeclared soy.
    Codes on the package
    all codes from 2011 through 2016
    Where it was sold
    Nationwide.
    Amount recalled
    2,600 6 oz jars and 5,500 3 oz jars
    Status
    Ended Sep 5, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1331-2016
    View in FDA's recall database
  2. ENDEDClass II · ModerateRecalled Mar 14, 2016

    Bakery Fresh Goodness Apple Strudel 5 count, 24oz, packaged in Plastic container, distributed by Kin...

    King Soopers is recalling Apple Strudel 5 Count because they were incorrectly labeled and does not declare pecans in the ingredient statement.

    King Soopers Bakery · Denver, CO

    Where it was sold: Distributed to Colorado, Wyoming, Utah, and New Mexico (149 King Soopers and City Market stores). No foreign or govt/military/VA consignees.

    Show details
    Product, as FDA describes it
    Bakery Fresh Goodness Apple Strudel 5 count, 24oz, packaged in Plastic container, distributed by King Soopers Bakery, Denver, CO.
    Reason, in FDA's words
    King Soopers is recalling Apple Strudel 5 Count because they were incorrectly labeled and does not declare pecans in the ingredient statement.
    Codes on the package
    Sell By date of 03/20/2016
    Where it was sold
    Distributed to Colorado, Wyoming, Utah, and New Mexico (149 King Soopers and City Market stores). No foreign or govt/military/VA consignees.
    Amount recalled
    up to 411 packages
    Status
    Ended Apr 29, 2016 (FDA lists it as terminated)
    FDA recall number
    F-0804-2016
    View in FDA's recall database
  3. ENDEDClass I · Most seriousRecalled Mar 10, 2016

    Korea chopped Kimchee packaged in 1 gallon, 1/2 gallon, 1/4 gallon, and 1/8 gallon packaged in glass...

    Undeclared anchovies in Kimchee product.

    Chicago Kimchee · Franklin Park, IL

    Where it was sold: Products were distributed to several distributors in the chicagoland area.

    Show details
    Product, as FDA describes it
    Korea chopped Kimchee packaged in 1 gallon, 1/2 gallon, 1/4 gallon, and 1/8 gallon packaged in glass jars inside plastic containers with multi colored label and black lettering.
    Reason, in FDA's words
    Undeclared anchovies in Kimchee product.
    Codes on the package
    This product does not contain any codes or expiration dates.
    Where it was sold
    Products were distributed to several distributors in the chicagoland area.
    Amount recalled
    1 gallon: 401 boxes, 4 jars/box 1/2 gallon: 167 boxes, 6 jars/box 1/4 gallon: 371 boxes, 12 jars/box 1/8 gallon: 113 boxes: 12 jars/box
    Status
    Ended Mar 19, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1096-2016
    View in FDA's recall database
  4. ENDEDClass I · Most seriousRecalled Mar 10, 2016

    Korea white Kimchee packaged in 1 gallon, 1/2 gallon, packaged in glass jars inside plastic containe...

    Undeclared anchovies in Kimchee product.

    Chicago Kimchee · Franklin Park, IL

    Where it was sold: Products were distributed to several distributors in the chicagoland area.

    Show details
    Product, as FDA describes it
    Korea white Kimchee packaged in 1 gallon, 1/2 gallon, packaged in glass jars inside plastic containers with multi colored label and black lettering.
    Reason, in FDA's words
    Undeclared anchovies in Kimchee product.
    Codes on the package
    This product does not contain any codes or expiration dates.
    Where it was sold
    Products were distributed to several distributors in the chicagoland area.
    Amount recalled
    1 gallon: 3 boxes, 4 jars/box, 1/2 gallon: 1 box, 6 jars/box
    Status
    Ended Mar 19, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1097-2016
    View in FDA's recall database
  5. ENDEDClass I · Most seriousRecalled Mar 10, 2016

    Korea whole Kimchee packaged in 1 gallon packaged in glass jars inside plastic containers with multi...

    Undeclared anchovies in Kimchee product.

    Chicago Kimchee · Franklin Park, IL

    Where it was sold: Products were distributed to several distributors in the chicagoland area.

    Show details
    Product, as FDA describes it
    Korea whole Kimchee packaged in 1 gallon packaged in glass jars inside plastic containers with multi colored label and black lettering.
    Reason, in FDA's words
    Undeclared anchovies in Kimchee product.
    Codes on the package
    This product does not contain any codes or expiration dates.
    Where it was sold
    Products were distributed to several distributors in the chicagoland area.
    Amount recalled
    1 gallon: 8 boxes, 4 jars/box
    Status
    Ended Mar 19, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1098-2016
    View in FDA's recall database
  6. ENDEDClass II · ModerateRecalled Mar 9, 2016

    Spaghetti Soup; Annie's Kitchen, 2966 Stumptown Rd, Ronks, PA 17572 16 FL OZ

    Spaghetti Soup failed to declare the wheat allergen in the spaghetti ingredient and milk allergen in the butter ingredient.

    Annie's Kitchen · Ronks, PA

    Where it was sold: PA (known)

    Show details
    Product, as FDA describes it
    Spaghetti Soup; Annie's Kitchen, 2966 Stumptown Rd, Ronks, PA 17572 16 FL OZ
    Reason, in FDA's words
    Spaghetti Soup failed to declare the wheat allergen in the spaghetti ingredient and milk allergen in the butter ingredient.
    Codes on the package
    no codes
    Where it was sold
    PA (known)
    Amount recalled
    35 cases, 12 pints/cs; 25 cases 12 Qt/cs
    Status
    Ended Feb 22, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1444-2017
    View in FDA's recall database
  7. ENDEDClass II · ModerateRecalled Mar 9, 2016

    Vegetable Soup; Annie's Kitchen; 2966 Stumptown Rd, Ronks, PA 17572 16 FL OZ

    Vegetable Soup failed to declare wheat allergen in the noodle ingredient.

    Annie's Kitchen · Ronks, PA

    Where it was sold: PA (known)

    Show details
    Product, as FDA describes it
    Vegetable Soup; Annie's Kitchen; 2966 Stumptown Rd, Ronks, PA 17572 16 FL OZ
    Reason, in FDA's words
    Vegetable Soup failed to declare wheat allergen in the noodle ingredient.
    Codes on the package
    no codes
    Where it was sold
    PA (known)
    Amount recalled
    35 cases - 12 pint/cs; 35 cases- 12 Qt/cs.
    Status
    Ended Feb 22, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1445-2017
    View in FDA's recall database
  8. ENDEDClass II · ModerateRecalled Mar 9, 2016

    365 Everyday Value Mango Frozen Fruit Bars 4 Bars-4 fl. oz. (118 mL) each-Net 16 fl. oz. (472 mL) in...

    Undeclared coconut

    Whole Foods Market · Austin, TX

    Where it was sold: AL, AZ, AR, CA, CO, CT, DC, FL, GA, HI, ID, KS, KY, LA, MD, MS, NJ, NM, NC, NV, NY, OH, OK, PA, SC, TX, TN, VT, VA, Canada

    UPC 099482413446
    Show details
    Product, as FDA describes it
    365 Everyday Value Mango Frozen Fruit Bars 4 Bars-4 fl. oz. (118 mL) each-Net 16 fl. oz. (472 mL) in a cardboard carton, UPC: 0-99482-41344-6, Distributed By: Whole Foods Market Austin, Texas 78703
    Reason, in FDA's words
    Undeclared coconut
    Codes on the package
    UPC: 9948241344 Best By: Dec 10 2016
    Where it was sold
    AL, AZ, AR, CA, CO, CT, DC, FL, GA, HI, ID, KS, KY, LA, MD, MS, NJ, NM, NC, NV, NY, OH, OK, PA, SC, TX, TN, VT, VA, Canada
    Amount recalled
    1336 cases (12 cartons per case)
    Status
    Ended Feb 17, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2290-2016
    View in FDA's recall database
  9. ENDEDClass I · Most seriousRecalled Mar 8, 2016

    Tuna Salad Sandwich, Net Wt. 4.5 oz (128g) sold under the following brands and UPC: 1. SuperMom's ...

    Supermom's identified that the Tuna Salad Sandwich contains an undeclared allergen (milk).

    Northern Tier Bakery (dba\ Super Mom's) · St Paul Park, MN

    Where it was sold: MN and WI only. No OUS distribution

    UPC 763913801248UPC 763913107029
    Show details
    Product, as FDA describes it
    Tuna Salad Sandwich, Net Wt. 4.5 oz (128g) sold under the following brands and UPC: 1. SuperMom's Bakery, UPC: 76391380124; 2. TakeAway Cafe, UPC: 76391310702; 3. Express Cafe, UPC: 76391380124 Keep Refrigerated.
    Reason, in FDA's words
    Supermom's identified that the Tuna Salad Sandwich contains an undeclared allergen (milk).
    Codes on the package
    Enjoy Through: 3/11
    Where it was sold
    MN and WI only. No OUS distribution
    Amount recalled
    385 sandwiches
    Status
    Ended May 25, 2016 (FDA lists it as terminated)
    FDA recall number
    F-1066-2016
    View in FDA's recall database
  10. ENDEDClass I · Most seriousRecalled Mar 4, 2016

    Eatin' Alive VEGAN GLUTEN FREE RAW thai peanut noodles. Keep Refrigerated. 8oz UPC 0 91037 56624 ...

    Paige Common dba Eatin' Alive is recalling Thai Peanut Noodles and Thai Wrap due to undeclared allergen soy. The soy is a sub ingredient of tamari.

    Paige Common · Portland, OR

    Where it was sold: Oregon retail stores only

    UPC 091037566249
    Show details
    Product, as FDA describes it
    Eatin' Alive VEGAN GLUTEN FREE RAW thai peanut noodles. Keep Refrigerated. 8oz UPC 0 91037 56624 9
    Reason, in FDA's words
    Paige Common dba Eatin' Alive is recalling Thai Peanut Noodles and Thai Wrap due to undeclared allergen soy. The soy is a sub ingredient of tamari.
    Codes on the package
    SELL BY: 3/8
    Where it was sold
    Oregon retail stores only
    Amount recalled
    24 units
    Status
    Ended Aug 23, 2016 (FDA lists it as terminated)
    FDA recall number
    F-1971-2016
    View in FDA's recall database
  11. ENDEDClass I · Most seriousRecalled Mar 4, 2016

    Eatin' Alive VEGAN GLUTEN FREE RAW thai wrap. Keep Refrigerated. 6oz UPC 0 91037 56620

    Paige Common dba Eatin' Alive is recalling Thai Peanut Noodles and Thai Wrap due to undeclared allergen soy. The soy is a sub ingredient of tamari.

    Paige Common · Portland, OR

    Where it was sold: Oregon retail stores only

    UPC 091037566201
    Show details
    Product, as FDA describes it
    Eatin' Alive VEGAN GLUTEN FREE RAW thai wrap. Keep Refrigerated. 6oz UPC 0 91037 56620
    Reason, in FDA's words
    Paige Common dba Eatin' Alive is recalling Thai Peanut Noodles and Thai Wrap due to undeclared allergen soy. The soy is a sub ingredient of tamari.
    Codes on the package
    SELL BY: 3/8
    Where it was sold
    Oregon retail stores only
    Amount recalled
    42 units
    Status
    Ended Aug 23, 2016 (FDA lists it as terminated)
    FDA recall number
    F-1972-2016
    View in FDA's recall database
  12. ENDEDClass II · ModerateRecalled Mar 3, 2016

    Duncan Hines Signature Swiss Chocolate Cake Mix, 16.5 oz. cartons, Distributed by: Pinnacle Foods, C...

    A natural flavoring containing a milk ingredient was inadvertently used to manufacture the Duncan Hines Signature Swiss Chocolate Cake Mix, 16.5 oz. c...

    Pinnacle Foods, LLC · Parsippany, NJ

    Where it was sold: FL and IL

    UPC 644209411207
    Show details
    Product, as FDA describes it
    Duncan Hines Signature Swiss Chocolate Cake Mix, 16.5 oz. cartons, Distributed by: Pinnacle Foods, Cherry Hill, New Jersey USA, UPC 6 44209 41120 7
    Reason, in FDA's words
    A natural flavoring containing a milk ingredient was inadvertently used to manufacture the Duncan Hines Signature Swiss Chocolate Cake Mix, 16.5 oz. cartons and the Duncan Hines Swiss Moist Deluxe Swiss Chocolate (Chocolate Suizo) 16.5 oz. cartons. The incorrect labeling was used on this product declaring that these products were a NON-milk containing product.
    Codes on the package
    Case Lot #6521017E31 with Best By: Jan 21 2017
    Where it was sold
    FL and IL
    Amount recalled
    240 cases
    Status
    Ended Aug 25, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1247-2016
    View in FDA's recall database
  13. ENDEDClass II · ModerateRecalled Mar 3, 2016

    Duncan Hines Moist Deluxe Swiss Chocolate (Chocolate Suizo) Cake Mix, Net Wt. 16.5 oz. (1 LB 5 oz.) ...

    A natural flavoring containing a milk ingredient was inadvertently used to manufacture the Duncan Hines Signature Swiss Chocolate Cake Mix, 16.5 oz. c...

    Pinnacle Foods, LLC · Parsippany, NJ

    Where it was sold: FL and IL

    Show details
    Product, as FDA describes it
    Duncan Hines Moist Deluxe Swiss Chocolate (Chocolate Suizo) Cake Mix, Net Wt. 16.5 oz. (1 LB 5 oz.) 468 g, Distributed by: Pinnacle Foods, Cherry Hill, New Jersey USA, UPC 6 44209 309748 7
    Reason, in FDA's words
    A natural flavoring containing a milk ingredient was inadvertently used to manufacture the Duncan Hines Signature Swiss Chocolate Cake Mix, 16.5 oz. cartons and the Duncan Hines Swiss Moist Deluxe Swiss Chocolate (Chocolate Suizo) 16.5 oz. cartons. The incorrect labeling was used on this product declaring that these products were a NON-milk containing product.
    Codes on the package
    Case Lot #6521017E31 with Best By: Jan 21 2017
    Where it was sold
    FL and IL
    Amount recalled
    1,600 cases
    Status
    Ended Aug 25, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1248-2016
    View in FDA's recall database
  14. ENDEDClass II · ModerateRecalled Mar 2, 2016

    MAGGI Chicken Flavor Bouillon 6Tab, 12Tab UPC Codes: 028000247959, 028000115678, 028000115678

    Nestle USA is recalling MAGGI Chicken Bouillon tablets because of undeclared wheat.

    Nestle USA · Glendale, CA

    Where it was sold: U.S. distribution to the following; CA, FL, TX, IL, GA, NJ, MI, MA, PA, NY, NC, OH, MD, NM, SC, AL, TN, OK, MS, AZ, ME, VA, NV, WY, UT, AL. No foreign distribution.

    UPC 028000247959UPC 028000115678
    Show details
    Product, as FDA describes it
    MAGGI Chicken Flavor Bouillon 6Tab, 12Tab UPC Codes: 028000247959, 028000115678, 028000115678
    Reason, in FDA's words
    Nestle USA is recalling MAGGI Chicken Bouillon tablets because of undeclared wheat.
    Codes on the package
    Production Codes: All Best Before ending in years 2015, 2016, 2017
    Where it was sold
    U.S. distribution to the following; CA, FL, TX, IL, GA, NJ, MI, MA, PA, NY, NC, OH, MD, NM, SC, AL, TN, OK, MS, AZ, ME, VA, NV, WY, UT, AL. No foreign distribution.
    Amount recalled
    558,325 units
    Status
    Ended Jun 29, 2016 (FDA lists it as terminated)
    FDA recall number
    F-0797-2016
    View in FDA's recall database
  15. ENDEDClass II · ModerateRecalled Mar 2, 2016

    Cheese & Fruit Bistro Box (Item #11015085), Starbucks brand. Product is packaged in plastic clamshe...

    The Cheese & Fruit Bistro Boxes are recalled because the product may contain an undeclared cashews.

    Gretchen's Shoebox Express · Seattle, WA

    Where it was sold: distributed in Washington.

    Show details
    Product, as FDA describes it
    Cheese & Fruit Bistro Box (Item #11015085), Starbucks brand. Product is packaged in plastic clamshell, net wt. 5.3 oz. The UPC is 7 62111 88146 5.
    Reason, in FDA's words
    The Cheese & Fruit Bistro Boxes are recalled because the product may contain an undeclared cashews.
    Codes on the package
    enjoy by date of March 4, 2016 and earlier
    Where it was sold
    distributed in Washington.
    Amount recalled
    13,268 units
    Status
    Ended Sep 8, 2016 (FDA lists it as terminated)
    FDA recall number
    F-1029-2016
    View in FDA's recall database
  16. ENDEDClass II · ModerateRecalled Mar 2, 2016

    Starbuck's Cheese & Fruit Bistro Box NET WT 5.3 OZ/150g packaged in non-flexible plastic container.

    Product may contain undeclared cashews.

    Flying Foods LLC · Grapevine, TX

    Where it was sold: FL, TX, OK

    Show details
    Product, as FDA describes it
    Starbuck's Cheese & Fruit Bistro Box NET WT 5.3 OZ/150g packaged in non-flexible plastic container.
    Reason, in FDA's words
    Product may contain undeclared cashews.
    Codes on the package
    Enjoy by 02/26, 02/27, 02/28, 02/29, 03/01, 03/02, 03/03, 03/04
    Where it was sold
    FL, TX, OK
    Amount recalled
    8,591 units
    Status
    Ended Feb 16, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1081-2016
    View in FDA's recall database
  17. ENDEDClass II · ModerateRecalled Mar 1, 2016

    Sea Salt Caramel Pretzel Ice Cream, Red Button Vintage Creamery, 56 fluid ounce, Paper Tub, 6 tubs p...

    Casper's Ice Cream is recalling "Sea Salt Caramel Pretzel" Ice Cream because it contains "Caramel Cashew" ice cream which presents a potential allerg...

    Casper's Ice Cream, Inc · Richmond, UT

    Where it was sold: Utah, Idaho, Montana, Nevada, Wyoming, Washington. No foreign or VA/govt/military consignees.

    UPC 077865010048
    Show details
    Product, as FDA describes it
    Sea Salt Caramel Pretzel Ice Cream, Red Button Vintage Creamery, 56 fluid ounce, Paper Tub, 6 tubs per case, Distributed by Associated Foods, Inc. Utah; Manufactured by Caspers Ice Cream, Inc. Utah
    Reason, in FDA's words
    Casper's Ice Cream is recalling "Sea Salt Caramel Pretzel" Ice Cream because it contains "Caramel Cashew" ice cream which presents a potential allergen threat.
    Codes on the package
    Lot # 3201561 xx:xx:xx (hour:minute:second) BB 05/16/2017 UPC 077865010048
    Where it was sold
    Utah, Idaho, Montana, Nevada, Wyoming, Washington. No foreign or VA/govt/military consignees.
    Amount recalled
    124 cases
    Status
    Ended Jun 15, 2016 (FDA lists it as terminated)
    FDA recall number
    F-0751-2016
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled Mar 1, 2016

    Almonds, dry roasted, not salted, packaged in 25 lb. cardboard cartons

    Cashews were mixed with almonds but allergen was not declared on outside packaging.

    Specialty Commodities, Inc. · Fargo, ND

    Where it was sold: CO, AZ, and CA. See distribution spreadsheet in the attached email.

    Show details
    Product, as FDA describes it
    Almonds, dry roasted, not salted, packaged in 25 lb. cardboard cartons
    Reason, in FDA's words
    Cashews were mixed with almonds but allergen was not declared on outside packaging.
    Codes on the package
    Item number ALMO-033; Manufacturer lot number 1050188-1-16007 (on container label); Warehouse lot number LV0206674
    Where it was sold
    CO, AZ, and CA. See distribution spreadsheet in the attached email.
    Amount recalled
    394 cases (9850 lbs.)
    Status
    Ended Feb 7, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1084-2016
    View in FDA's recall database
  19. ENDEDClass II · ModerateRecalled Feb 25, 2016

    Dried lactose powder, product sold under brand Wine-King Beer-King, packaged in three consumer-size...

    Dried Lactose powder product, which is used in brewery to make beer, does not declare whey or milk and the label declared lactose only.

    Northwest Specialty, Inc. · Lakewood, WA

    Where it was sold: distributed in AK, OR, and WA

    Show details
    Product, as FDA describes it
    Dried lactose powder, product sold under brand Wine-King Beer-King, packaged in three consumer-sized plastic bags of 4 oz., 1 Lb. and 5 Lb. net weight.
    Reason, in FDA's words
    Dried Lactose powder product, which is used in brewery to make beer, does not declare whey or milk and the label declared lactose only.
    Codes on the package
    None
    Where it was sold
    distributed in AK, OR, and WA
    Amount recalled
    55/4 oz. bags; 247/1 lb. bags; and 45/5 lbs. bags
    Status
    Ended Nov 2, 2016 (FDA lists it as terminated)
    FDA recall number
    F-0784-2016
    View in FDA's recall database
  20. ENDEDClass I · Most seriousRecalled Feb 23, 2016

    Dark Chocolate Covered Coffee Beans, packaged in 12 oz. tubs

    Lipari Foods, LLC has issued a voluntary recall of dark chocolate covered coffee beans packaged by sister company JLM due to an undeclared allergen of...

    Lipari Foods, Inc. · Warren, MI

    Where it was sold: Domestic: Indiana, Kentucky, Michigan, Ohio, Pennsylvania, Tennessee, Wisconsin and West Virginia. Foreign: None VA/DOD: None

    UPC 094776131761
    Show details
    Product, as FDA describes it
    Dark Chocolate Covered Coffee Beans, packaged in 12 oz. tubs
    Reason, in FDA's words
    Lipari Foods, LLC has issued a voluntary recall of dark chocolate covered coffee beans packaged by sister company JLM due to an undeclared allergen of tree nuts (almonds).
    Codes on the package
    Dark Chocolate Covered Coffee Beans, packaged in 12 oz. tubs; (Multiple Brands including: Angeli Foods, Hardings Markets, Goosberries Fresh Food Market, Marthas Vineyard, Hollywood Market, Daniels Foods, Snooks Butcher Shoppe, Martins, Holiday Market, The Purple Onion, Remke Market) Lipari Product Number 510526, Lot # 22201512, Weight 12oz Tubs, Best By Date: 12/21/16, UPC # 094776131761; and Generic brand Lipari Product Number 477308, Lot # 22201512, Weight 12oz Tubs, Best By Date: 12/21/16, and UPC # 094776131761.
    Where it was sold
    Domestic: Indiana, Kentucky, Michigan, Ohio, Pennsylvania, Tennessee, Wisconsin and West Virginia. Foreign: None VA/DOD: None
    Amount recalled
    26 cases  477308 (Tub LG Dark Chocolate Coffee Beans 12-12oz) & 17 cases  510526 (Tub LG PL Dark Chocolate Coffee Beans 12-12oz)
    Status
    Ended Feb 8, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0776-2016
    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.