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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

7,651 recalls · showing 4,801 to 4,820

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  1. ENDEDClass II · ModerateRecalled Dec 20, 2016

    Cracker Jax, Hungry Heart brand, packaged in a clear Cello bag, heat sealed. Net wt. 8 oz. (227g).

    Cracker Jax are recalled because butter is declared, but milk is not declared, and soy (from the pan release agent spray) is not declared

    Hungry Heart Bakery · Portland, OR

    Where it was sold: distributed in OR

    Show details
    Product, as FDA describes it
    Cracker Jax, Hungry Heart brand, packaged in a clear Cello bag, heat sealed. Net wt. 8 oz. (227g).
    Reason, in FDA's words
    Cracker Jax are recalled because butter is declared, but milk is not declared, and soy (from the pan release agent spray) is not declared
    Codes on the package
    none
    Where it was sold
    distributed in OR
    Amount recalled
    6 packages
    Status
    Ended Mar 7, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1275-2017
    View in FDA's recall database
  2. ENDEDClass II · ModerateRecalled Dec 19, 2016

    ALN UNICED 1/4 Sheet Split Layer White Cake, Item 00886, three stacked cake layers with plastic line...

    ALN UNICED ¿ Sheet Split Layer White Cake, a box of 12 cakes, is recalled due to a potential contamination with walnut and label does not declare waln...

    Portland Specialty Baking LLC · Portland, OR

    Where it was sold: distributed in CA only

    UPC 750903008862
    Show details
    Product, as FDA describes it
    ALN UNICED 1/4 Sheet Split Layer White Cake, Item 00886, three stacked cake layers with plastic liner in between layers are packaged in a corrugated box, a total of 12 cakes per bulk box. UPC 00750903008862
    Reason, in FDA's words
    ALN UNICED ¿ Sheet Split Layer White Cake, a box of 12 cakes, is recalled due to a potential contamination with walnut and label does not declare walnut.
    Codes on the package
    -MFG Date 6237, Manufacture Date: 08-24-2016. -MFG Date 6285, Manufacture Date: 10-11-2016. -MFG Date 6286, Manufacture Date: 10-12-2016.
    Where it was sold
    distributed in CA only
    Amount recalled
    3314 cases
    Status
    Ended Apr 3, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1223-2017
    View in FDA's recall database
  3. ENDEDClass II · ModerateRecalled Dec 19, 2016

    Gonsalves Sugar Coated Almonds, Net Wt. 12 oz. Distributed by The Gonsalves Company, Smithfield, RI...

    Product contains undeclared wheat, Red #3, Red #40, Blue #1, Yellow # 6

    The Henry Gonsalves Co. · Smithfield, RI

    Where it was sold: CT, MA NJ, NY, RI

    Show details
    Product, as FDA describes it
    Gonsalves Sugar Coated Almonds, Net Wt. 12 oz. Distributed by The Gonsalves Company, Smithfield, RI 02917 UPC number 20539-64550
    Reason, in FDA's words
    Product contains undeclared wheat, Red #3, Red #40, Blue #1, Yellow # 6
    Codes on the package
    All product distributed prior to Dec 12, 2106
    Where it was sold
    CT, MA NJ, NY, RI
    Amount recalled
    75 cases
    Status
    Ended Apr 6, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1338-2017
    View in FDA's recall database
  4. ENDEDClass I · Most seriousRecalled Dec 18, 2016

    Winco Foods Creamy Ranch Dressing 16 fl oz. UPC Code: 0 70552 70103 8

    Undeclared egg.

    Vanlaw Food Products, Inc · Fullerton, CA

    Where it was sold: U.S. distribution to the following; OR, ID, CA, TX, AZ. No foreign distribution.

    UPC 070552701038
    Show details
    Product, as FDA describes it
    Winco Foods Creamy Ranch Dressing 16 fl oz. UPC Code: 0 70552 70103 8
    Reason, in FDA's words
    Undeclared egg.
    Codes on the package
    BEST BY 08/23/17
    Where it was sold
    U.S. distribution to the following; OR, ID, CA, TX, AZ. No foreign distribution.
    Amount recalled
    2,738 cases
    Status
    Ended Mar 28, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1180-2017
    View in FDA's recall database
  5. ENDEDClass I · Most seriousRecalled Dec 17, 2016

    Chocolate Premium Chocolate Treats Vanilla Caramels packaged under the following labels: (1) Weig...

    Product contains undeclared peanuts

    New American Food Products, LLC. · Methuen, MA

    Where it was sold: TN

    UPC 024354705039UPC 483743202045
    Show details
    Product, as FDA describes it
    Chocolate Premium Chocolate Treats Vanilla Caramels packaged under the following labels: (1) Weigel's Mountain Valley Premium Chocolate Treats Milk Chocolate Vanilla Caramels, 2.75 oz (78g) Tube snack Bag UPC Code: 024354705039; (2) Royal Farms Market Place Premium Chocolate Treats Milk Chocolate Vanilla Caramels 2.75 oz (78g) Tube snack Bag UPC Code: 483743202045
    Reason, in FDA's words
    Product contains undeclared peanuts
    Codes on the package
    (1)Best by date: 11 14 17; (2) Best by date: 12 08 17
    Where it was sold
    TN
    Amount recalled
    (1) 220 Cases (2640 units); (2) 44 cases (6336 units)
    Status
    Ended Aug 2, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1428-2017
    View in FDA's recall database
  6. ENDEDClass I · Most seriousRecalled Dec 14, 2016

    Cranberry Orange Scone, brand Mad Batter Bakery, net wt. 5 oz per unit. Product is sold in a plasti...

    Cranberry Orange Scones are recalled because they may contain undeclared Milk, Egg, Soy, and Wheat.

    Thomas Hammer Coffee Roasters, Inc. · Spokane, WA

    Where it was sold: distributed in WA

    Show details
    Product, as FDA describes it
    Cranberry Orange Scone, brand Mad Batter Bakery, net wt. 5 oz per unit. Product is sold in a plastic film wrapper with labeling on the back of the package.
    Reason, in FDA's words
    Cranberry Orange Scones are recalled because they may contain undeclared Milk, Egg, Soy, and Wheat.
    Codes on the package
    no codes
    Where it was sold
    distributed in WA
    Amount recalled
    52/ 5 oz. units
    Status
    Ended Jan 12, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1085-2017
    View in FDA's recall database
  7. ENDEDClass II · ModerateRecalled Dec 14, 2016

    Birdman Bread, each loaf has net wt. 24 oz and 32 oz.. The UPC code ia 6 36428 10200 4.

    Birdman Bread is recalled due to undeclared soy lecithin. The soy allergen is present in DDA pan spray (release agent) and the firm used it to spray t...

    Great Northern Bakehouse Inc. dba Le Petit Outre · Missoula, MT

    Where it was sold: distributed in MT only

    Show details
    Product, as FDA describes it
    Birdman Bread, each loaf has net wt. 24 oz and 32 oz.. The UPC code ia 6 36428 10200 4.
    Reason, in FDA's words
    Birdman Bread is recalled due to undeclared soy lecithin. The soy allergen is present in DDA pan spray (release agent) and the firm used it to spray the loaf pans.
    Codes on the package
    Pull by date of 12/15, 12/16, 12/17, and 12/18.
    Where it was sold
    distributed in MT only
    Amount recalled
    417 units total
    Status
    Ended Feb 9, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1253-2017
    View in FDA's recall database
  8. ENDEDClass II · ModerateRecalled Dec 14, 2016

    Whole Wheat Bread, each loaf has a net wt. 32 oz.. The UPC is code 6 36428 50200 2.

    Whole Wheat Bread is recalled due to undeclared soy lecithin. The soy allergen is present in DDA pan spray (release agent) and the firm used it to spr...

    Great Northern Bakehouse Inc. dba Le Petit Outre · Missoula, MT

    Where it was sold: distributed in MT only

    Show details
    Product, as FDA describes it
    Whole Wheat Bread, each loaf has a net wt. 32 oz.. The UPC is code 6 36428 50200 2.
    Reason, in FDA's words
    Whole Wheat Bread is recalled due to undeclared soy lecithin. The soy allergen is present in DDA pan spray (release agent) and the firm used it to spray the loaf pans.
    Codes on the package
    Pull by date of 12/15 and 12/16
    Where it was sold
    distributed in MT only
    Amount recalled
    103 units
    Status
    Ended Feb 9, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1254-2017
    View in FDA's recall database
  9. ENDEDClass II · ModerateRecalled Dec 14, 2016

    Daily Wheat Bread, each loaf has a net wt. 24 oz.. The UPC is code and 6 36428 50500 3.

    Daily Wheat Bread is recalled due to undeclared soy lecithin. The soy allergen is present in DDA pan spray (release agent) and the firm used it to spr...

    Great Northern Bakehouse Inc. dba Le Petit Outre · Missoula, MT

    Where it was sold: distributed in MT only

    Show details
    Product, as FDA describes it
    Daily Wheat Bread, each loaf has a net wt. 24 oz.. The UPC is code and 6 36428 50500 3.
    Reason, in FDA's words
    Daily Wheat Bread is recalled due to undeclared soy lecithin. The soy allergen is present in DDA pan spray (release agent) and the firm used it to spray the loaf pans.
    Codes on the package
    Pull by date of 12/15, 12/16, 12/17, and 12/18.
    Where it was sold
    distributed in MT only
    Amount recalled
    24 units
    Status
    Ended Feb 9, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1255-2017
    View in FDA's recall database
  10. ENDEDClass II · ModerateRecalled Dec 14, 2016

    Italian Deli Loaf, each loaf has a net wt. 32 oz.. The UPC is code 6 36428 50200 2.

    Italian Deli Loaf is recalled due to undeclared soy lecithin. The soy allergen is present in DDA pan spray (release agent) and the firm used it to spr...

    Great Northern Bakehouse Inc. dba Le Petit Outre · Missoula, MT

    Where it was sold: distributed in MT only

    Show details
    Product, as FDA describes it
    Italian Deli Loaf, each loaf has a net wt. 32 oz.. The UPC is code 6 36428 50200 2.
    Reason, in FDA's words
    Italian Deli Loaf is recalled due to undeclared soy lecithin. The soy allergen is present in DDA pan spray (release agent) and the firm used it to spray the loaf pans.
    Codes on the package
    Pull by date of 12/15 and 12/16.
    Where it was sold
    distributed in MT only
    Amount recalled
    72 units
    Status
    Ended Feb 9, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1256-2017
    View in FDA's recall database
  11. ENDEDClass II · ModerateRecalled Dec 14, 2016

    Sourdough Deli Loaf, each loaf has a net wt. 28 oz.. The UPC is code 6 36428 50200 2

    Sourdough Deli Loaf is recalled due to undeclared soy lecithin. The soy allergen is present in DDA pan spray (release agent) and the firm used it to s...

    Great Northern Bakehouse Inc. dba Le Petit Outre · Missoula, MT

    Where it was sold: distributed in MT only

    Show details
    Product, as FDA describes it
    Sourdough Deli Loaf, each loaf has a net wt. 28 oz.. The UPC is code 6 36428 50200 2
    Reason, in FDA's words
    Sourdough Deli Loaf is recalled due to undeclared soy lecithin. The soy allergen is present in DDA pan spray (release agent) and the firm used it to spray the loaf pans.
    Codes on the package
    Pull by date of 12/15 and 12/16.
    Where it was sold
    distributed in MT only
    Amount recalled
    165 units
    Status
    Ended Feb 9, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1257-2017
    View in FDA's recall database
  12. ENDEDClass II · ModerateRecalled Dec 14, 2016

    Brewers Grain Deli Loaf, each loaf has a net wt. 24 oz.. The UPC code is 6 36428 10300 1.

    Brewers Grain Deli Loaf is recalled due to undeclared soy lecithin. The soy allergen is present in DDA pan spray (release agent) and the firm used it ...

    Great Northern Bakehouse Inc. dba Le Petit Outre · Missoula, MT

    Where it was sold: distributed in MT only

    Show details
    Product, as FDA describes it
    Brewers Grain Deli Loaf, each loaf has a net wt. 24 oz.. The UPC code is 6 36428 10300 1.
    Reason, in FDA's words
    Brewers Grain Deli Loaf is recalled due to undeclared soy lecithin. The soy allergen is present in DDA pan spray (release agent) and the firm used it to spray the loaf pans.
    Codes on the package
    Pull by date of 12/15, 12/16, 12/17, and 12/18.
    Where it was sold
    distributed in MT only
    Amount recalled
    55 units
    Status
    Ended Feb 9, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1258-2017
    View in FDA's recall database
  13. ENDEDClass II · ModerateRecalled Dec 14, 2016

    NY Rye Deli Loaf, each loaf has a net wt. 32 oz.. No UPC as this is for food service only.

    NY Rye Deli Loaf is recalled due to undeclared soy lecithin. The soy allergen is present in DDA pan spray (release agent) and the firm used it to spra...

    Great Northern Bakehouse Inc. dba Le Petit Outre · Missoula, MT

    Where it was sold: distributed in MT only

    Show details
    Product, as FDA describes it
    NY Rye Deli Loaf, each loaf has a net wt. 32 oz.. No UPC as this is for food service only.
    Reason, in FDA's words
    NY Rye Deli Loaf is recalled due to undeclared soy lecithin. The soy allergen is present in DDA pan spray (release agent) and the firm used it to spray the loaf pans.
    Codes on the package
    Pull by date of 12/15 and 12/16
    Where it was sold
    distributed in MT only
    Amount recalled
    89 units
    Status
    Ended Feb 9, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1259-2017
    View in FDA's recall database
  14. ENDEDClass I · Most seriousRecalled Dec 13, 2016

    Linden's brand Chocolate Chip Cookies: a) Chocolate Chippers Bite Size Cookies (Mini), NET WT. 2 OZ...

    The product contains undeclared milk from the bulk chocolate chips received from the supplier.

    Linden Cookies, Inc · Congers, NY

    Where it was sold: Florida, Virginia, Maryland, Delaware, New Jersey, New York, Connecticut, and Massachusetts

    UPC 076809300177UPC 076809300900UPC 076809300108
    Show details
    Product, as FDA describes it
    Linden's brand Chocolate Chip Cookies: a) Chocolate Chippers Bite Size Cookies (Mini), NET WT. 2 OZ., UPC 76809-30017; b) Chocolate Chippers (Mini), NET WT 1.1 OZ., UPC 76809-30090; c) 3 LARGE CHOCOLATE CHIP COOKIES (Pack), NET WT. 1.75 OZ. UPC 76809-30010 --- LINDEN COOKIES, INC. 25 BRENNER DRIVE CONGERS, NY 10920
    Reason, in FDA's words
    The product contains undeclared milk from the bulk chocolate chips received from the supplier.
    Codes on the package
    a): Sell By Dates Feb. 8, 2017 through March 28, 2017; b): Sell By Dates Feb. 8, 2017 through March 28, 2017; c): Dec. 14, 2016 through Feb 01, 2017
    Where it was sold
    Florida, Virginia, Maryland, Delaware, New Jersey, New York, Connecticut, and Massachusetts
    Amount recalled
    2 oz.: 864,810 packages; 1.1 oz.: 962,316 packages
    Status
    Ended Aug 17, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1222-2017
    View in FDA's recall database
  15. ENDEDClass I · Most seriousRecalled Dec 12, 2016

    4 oz. Complete Cookie, Chocolate Chip, UPC Code: 7 87692-83461 7, 12pks: 231,114 sleeves (contains...

    Lenny & Larrys is recalling Chocolate Chip and Coconut Chocolate Chip cookies due to the possible presence of undeclared milk in the dark chocolate c...

    Lenny & Larry's, Inc. · Panorama City, CA

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

    Where it was sold: US and worldwide: Kuwait, Dubai, United Kingdom, Israel, Australia, Mexico, Dominican Republic, Sweden, Colombia, Canada, Brazil, Panama, Netherlands, Norway, Philippines, Saudi Ar...

    UPC 787692834617
    Show details
    Product, as FDA describes it
    4 oz. Complete Cookie, Chocolate Chip, UPC Code: 7 87692-83461 7, 12pks: 231,114 sleeves (contains 12 cookies) 6pks: 54,660 sleeves (contains 6 cookies) 4pks: 795,528 sleeves (contains 4) Total cookies from all pack sizes above: 6,283,440
    Reason, in FDA's words
    Lenny & Larrys is recalling Chocolate Chip and Coconut Chocolate Chip cookies due to the possible presence of undeclared milk in the dark chocolate chips.
    Codes on the package
    7-1-17, 7-27-17, 7-28-17, 7-29-17, 7-30-17, 8-03-17, 8-04-17, 8-05-17, 8-06-17, 8-07-17, 8-10-17, 8-11-17, 8-12-17, 8-15-17, 8-16-17, 8-17-17, 8-18-17, 8-19-17, 8-20-17, 8-25-17, 8-26-17, 8-27-17, 8-29-17, 8-30-17, 8-31-17, 9-1-17, 9-06-17, 9-07-17, 9-08-17, 9-09-17, 9-10-17, 9-29-17, 10-3-17, 10-04-17, 10-05-17, 10-08-17, 10-13-17, 10-24-17, 11-07-17, 11-08-17, 11-09-17, 11-10-17, 11-14-17, 11-15-17, 11-16-17, 11-17-17, 11-21-17, 11-22-17, 11-23-17, 11-30-17, 20160701, 20160708, 20160709, 20160711, 20160712, 20160721, 20160722, 20160803, 20160804, 20160815, 20160816, 20160829, 20160830, 20160902, 20160906, 20160906, 20160908, 20160909, 20160913, 20160914, 20160915, 20160916, 20160928, 20160929, 20160930, 20161001, 20161003, 20161004, 20161005, 20161011, 20161012, 20161013, 20161020, 20161021, 20161110
    Where it was sold
    US and worldwide: Kuwait, Dubai, United Kingdom, Israel, Australia, Mexico, Dominican Republic, Sweden, Colombia, Canada, Brazil, Panama, Netherlands, Norway, Philippines, Saudi Arabia, Peru, Singapore, Korea, Russia,
    Amount recalled
    5,232,888 units
    Status
    Ended May 31, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1220-2017
    View in FDA's recall database
  16. ENDEDClass I · Most seriousRecalled Dec 12, 2016

    4 oz. Complete Cookie, Coconut Chocolate Chip, UPC Code: 7 87692-83538 6, 12pks: 15,834 sleeves (c...

    Lenny & Larrys is recalling Chocolate Chip and Coconut Chocolate Chip cookies due to the possible presence of undeclared milk in the dark chocolate ch...

    Lenny & Larry's, Inc. · Panorama City, CA

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

    Where it was sold: US and worldwide: Kuwait, Dubai, United Kingdom, Israel, Australia, Mexico, Dominican Republic, Sweden, Colombia, Canada, Brazil, Panama, Netherlands, Norway, Philippines, Saudi Ar...

    UPC 787692835386
    Show details
    Product, as FDA describes it
    4 oz. Complete Cookie, Coconut Chocolate Chip, UPC Code: 7 87692-83538 6, 12pks: 15,834 sleeves (contains 12 cookies) Total cookies from pack sizes above: 190,008
    Reason, in FDA's words
    Lenny & Larrys is recalling Chocolate Chip and Coconut Chocolate Chip cookies due to the possible presence of undeclared milk in the dark chocolate chips.
    Codes on the package
    9-18-17, 9-19-17, 10-19-17, 10-20-17, 11-14-17, 11-15-17
    Where it was sold
    US and worldwide: Kuwait, Dubai, United Kingdom, Israel, Australia, Mexico, Dominican Republic, Sweden, Colombia, Canada, Brazil, Panama, Netherlands, Norway, Philippines, Saudi Arabia, Peru, Singapore, Korea, Russia,
    Amount recalled
    176,544 units
    Status
    Ended May 31, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1221-2017
    View in FDA's recall database
  17. ENDEDClass II · ModerateRecalled Dec 11, 2016

    White Fudge Oreo, brand Real Fudge. Product is sold in clear plastic deli container in 8 oz. and 16 ...

    White Fudge Oreo is recalled due to undeclared wheat and blue # 1.

    Real Fudge · Mesa, WA

    Where it was sold: Distributed in Idaho, Maryland, Nevada, Oregon, and Washington

    Show details
    Product, as FDA describes it
    White Fudge Oreo, brand Real Fudge. Product is sold in clear plastic deli container in 8 oz. and 16 oz.
    Reason, in FDA's words
    White Fudge Oreo is recalled due to undeclared wheat and blue # 1.
    Codes on the package
    no codes
    Where it was sold
    Distributed in Idaho, Maryland, Nevada, Oregon, and Washington
    Amount recalled
    65/8 oz. units and 2/16 oz. units
    Status
    Ended Jan 31, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0753-2017
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled Dec 11, 2016

    Peanut Butter Fudge, brand Real Fudge. Product is sold in clear plastic deli container in 8, 12, and...

    Peanut Butter Fudge is recalled due to undeclared blue #1.

    Real Fudge · Mesa, WA

    Where it was sold: Distributed in Idaho, Maryland, Nevada, Oregon, and Washington

    Show details
    Product, as FDA describes it
    Peanut Butter Fudge, brand Real Fudge. Product is sold in clear plastic deli container in 8, 12, and 16 oz.
    Reason, in FDA's words
    Peanut Butter Fudge is recalled due to undeclared blue #1.
    Codes on the package
    no codes
    Where it was sold
    Distributed in Idaho, Maryland, Nevada, Oregon, and Washington
    Amount recalled
    78/8 oz. units; 60/12 oz. units; and 7/16 oz. units
    Status
    Ended Jan 31, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0756-2017
    View in FDA's recall database
  19. ENDEDClass II · ModerateRecalled Dec 11, 2016

    Coconut Fudge, brand Real Fudge. Product is sold in clear plastic deli container in 8 oz.

    Coconut Fudge is recalled due to undeclared blue #1.

    Real Fudge · Mesa, WA

    Where it was sold: Distributed in Idaho, Maryland, Nevada, Oregon, and Washington

    Show details
    Product, as FDA describes it
    Coconut Fudge, brand Real Fudge. Product is sold in clear plastic deli container in 8 oz.
    Reason, in FDA's words
    Coconut Fudge is recalled due to undeclared blue #1.
    Codes on the package
    no codes
    Where it was sold
    Distributed in Idaho, Maryland, Nevada, Oregon, and Washington
    Amount recalled
    22/8 oz. units
    Status
    Ended Jan 31, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0761-2017
    View in FDA's recall database
  20. ENDEDClass II · ModerateRecalled Dec 9, 2016

    The Sweet Dessert Corp., Cheesecake Cherry, Peso Neto (Net Weight) 3oz and 4 oz., Carr. 173 Km 7.1 B...

    Undeclared milk and food color: Red #40

    Sweets & Desserts, Inc. · Aguas Buenas, PR

    Where it was sold: Puerto Rico only

    Show details
    Product, as FDA describes it
    The Sweet Dessert Corp., Cheesecake Cherry, Peso Neto (Net Weight) 3oz and 4 oz., Carr. 173 Km 7.1 Bo. Sumidero, Aguas Buenas, P.R. 00703
    Reason, in FDA's words
    Undeclared milk and food color: Red #40
    Codes on the package
    Unknown
    Where it was sold
    Puerto Rico only
    Amount recalled
    384 units
    Status
    Ended Oct 15, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1598-2017
    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.