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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 4,461 to 4,480

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  1. ENDEDClass II · ModerateRecalled Jan 26, 2017

    White Chocolate Toffee, 2.2oz pouches, 6oz pouches, 7oz boxes, one pound boxes

    Bell Stone Toffee initiated a voluntary recall of all lots of White Chocolate Toffee, Dark Chocolate Toffee, and Toffee Chocolate Bars due to labeling...

    Bell Stone Toffee · Novi, MI

    Where it was sold: Domestic: MI, FL, MA, TX, GA, CO, OH Firm updated customer list to include out of state customers on 02/09/2017. Foreign:None V/A: None

    Show details
    Product, as FDA describes it
    White Chocolate Toffee, 2.2oz pouches, 6oz pouches, 7oz boxes, one pound boxes
    Reason, in FDA's words
    Bell Stone Toffee initiated a voluntary recall of all lots of White Chocolate Toffee, Dark Chocolate Toffee, and Toffee Chocolate Bars due to labeling that declared butter as an ingredient but failed to identify the allergen milk was present in products.
    Codes on the package
    All Lots with Best By Dates Between November 18, 2016 and March 18, 2017
    Where it was sold
    Domestic: MI, FL, MA, TX, GA, CO, OH Firm updated customer list to include out of state customers on 02/09/2017. Foreign:None V/A: None
    Amount recalled
    unknown
    Status
    Ended Jun 1, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1545-2017
    View in FDA's recall database
  2. ENDEDClass II · ModerateRecalled Jan 26, 2017

    Dark Chocolate Toffee, 2.2oz pouches, 6oz pouches, 7oz boxes, one pound boxes

    Bell Stone Toffee initiated a voluntary recall of all lots of White Chocolate Toffee, Dark Chocolate Toffee, and Toffee Chocolate Bars due to labeling...

    Bell Stone Toffee · Novi, MI

    Where it was sold: Domestic: MI, FL, MA, TX, GA, CO, OH Firm updated customer list to include out of state customers on 02/09/2017. Foreign:None V/A: None

    Show details
    Product, as FDA describes it
    Dark Chocolate Toffee, 2.2oz pouches, 6oz pouches, 7oz boxes, one pound boxes
    Reason, in FDA's words
    Bell Stone Toffee initiated a voluntary recall of all lots of White Chocolate Toffee, Dark Chocolate Toffee, and Toffee Chocolate Bars due to labeling that declared butter as an ingredient but failed to identify the allergen milk was present in products.
    Codes on the package
    All Lots with Best By Dates Between November 18, 2016 and March 18, 2017
    Where it was sold
    Domestic: MI, FL, MA, TX, GA, CO, OH Firm updated customer list to include out of state customers on 02/09/2017. Foreign:None V/A: None
    Amount recalled
    unknown
    Status
    Ended Jun 1, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1546-2017
    View in FDA's recall database
  3. ENDEDClass II · ModerateRecalled Jan 26, 2017

    Toffee Chocolate Bar, 3.5 oz

    Bell Stone Toffee initiated a voluntary recall of all lots of White Chocolate Toffee, Dark Chocolate Toffee, and Toffee Chocolate Bars due to labeling...

    Bell Stone Toffee · Novi, MI

    Where it was sold: Domestic: MI, FL, MA, TX, GA, CO, OH Firm updated customer list to include out of state customers on 02/09/2017. Foreign:None V/A: None

    Show details
    Product, as FDA describes it
    Toffee Chocolate Bar, 3.5 oz
    Reason, in FDA's words
    Bell Stone Toffee initiated a voluntary recall of all lots of White Chocolate Toffee, Dark Chocolate Toffee, and Toffee Chocolate Bars due to labeling that declared butter as an ingredient but failed to identify the allergen milk was present in products.
    Codes on the package
    All Lots with Best By Dates Between November 18, 2016 and March 18, 2017
    Where it was sold
    Domestic: MI, FL, MA, TX, GA, CO, OH Firm updated customer list to include out of state customers on 02/09/2017. Foreign:None V/A: None
    Amount recalled
    unknown
    Status
    Ended Jun 1, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1547-2017
    View in FDA's recall database
  4. ENDEDClass II · ModerateRecalled Jan 25, 2017

    MARICH Premium Chocolates; Chocolate Caramel Heart; Our delicious caramel hearts in rich milk and d...

    Firm received report of customer finding the incorrect product in the Caramel Heart box. The product inside was Triple Chocolate Toffee which contains...

    Marich Confectionery Company, Inc. · Hollister, CA

    Where it was sold: CA, MN and OK.

    UPC 797817444409
    Show details
    Product, as FDA describes it
    MARICH Premium Chocolates; Chocolate Caramel Heart; Our delicious caramel hearts in rich milk and dark chocolate; Net Wt 4.25 oz. (120g) UPC 797817-44440-9
    Reason, in FDA's words
    Firm received report of customer finding the incorrect product in the Caramel Heart box. The product inside was Triple Chocolate Toffee which contains almonds that are not listed in the Caramel Hearts ingredient list.
    Codes on the package
    Lot 0031711; Best by Date: 9/30/17.
    Where it was sold
    CA, MN and OK.
    Amount recalled
    30 cases (12 x 4.25 oz. boxes per case)
    Status
    Ended Mar 20, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1451-2017
    View in FDA's recall database
  5. ENDEDClass I · Most seriousRecalled Jan 24, 2017

    Bakery Fresh Goodness Carrot Cupcakes sold in 6 ct. 12 ct. and 25 ct. hard plastic container. Bak...

    Bakery Fresh Goodness Carrot Cupcakes are recalled due to undeclared milk and soy.

    Fred Meyers Inc · Portland, OR

    Where it was sold: distributed in Alaska, Idaho, Oregon, and Washington

    UPC 041573277314UPC 041573277321UPC 041573277338
    Show details
    Product, as FDA describes it
    Bakery Fresh Goodness Carrot Cupcakes sold in 6 ct. 12 ct. and 25 ct. hard plastic container. Bakery Fresh Goodness Carrot Cupcakes, 6 count package, UPC 41573-27731; Bakery Fresh Goodness Carrot Cupcakes, 12 count package, UPC 41573-27732; Bakery Fresh Goodness Carrot Cupcakes, 25 count package, UPC 41573-27733.
    Reason, in FDA's words
    Bakery Fresh Goodness Carrot Cupcakes are recalled due to undeclared milk and soy.
    Codes on the package
    Sell By 1/30/17 OR BEFORE
    Where it was sold
    distributed in Alaska, Idaho, Oregon, and Washington
    Amount recalled
    firm reported unknown amount
    Status
    Ended Mar 29, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1536-2017
    View in FDA's recall database
  6. ENDEDClass II · ModerateRecalled Jan 24, 2017

    Market Basket moreBAR Dark Chocolate Peanut , 4.3 oz. bar

    Product contains undeclared walnuts.

    DeMoulas Supermarket, Inc. · Tewksbury, MA

    Where it was sold: Product was distributed at Market Basket Supermarket Stores

    Show details
    Product, as FDA describes it
    Market Basket moreBAR Dark Chocolate Peanut , 4.3 oz. bar
    Reason, in FDA's words
    Product contains undeclared walnuts.
    Codes on the package
    Lot# 2176P
    Where it was sold
    Product was distributed at Market Basket Supermarket Stores
    Amount recalled
    3600 sleeves, 12 per sleeve
    Status
    Ended Jun 30, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2382-2017
    View in FDA's recall database
  7. ENDEDClass II · ModerateRecalled Jan 23, 2017

    Hot Barbecue Sauce; Net wt. 16 ounces; Manufactured by Carriage House Creations, 544 Gordon Alley,...

    Carriage House Creations is recalling 3 varieties of Bourbon Basting Sauce and Hot BBQ Sauce due to undeclared peanuts and soy. The recall was initiat...

    Carriage House Creations · Reynoldsville, PA

    Where it was sold: PA

    Show details
    Product, as FDA describes it
    Hot Barbecue Sauce; Net wt. 16 ounces; Manufactured by Carriage House Creations, 544 Gordon Alley, Reynoldsville, PA 15851;
    Reason, in FDA's words
    Carriage House Creations is recalling 3 varieties of Bourbon Basting Sauce and Hot BBQ Sauce due to undeclared peanuts and soy. The recall was initiated after receiving notification that the Worcestershire sauce ingredient was recalled for the undeclared allergens.
    Codes on the package
    Batch #3131601; Best If Used By: 5082018
    Where it was sold
    PA
    Amount recalled
    23 cases, 12 bottles/case
    Status
    Ended Nov 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1667-2017
    View in FDA's recall database
  8. ENDEDClass II · ModerateRecalled Jan 23, 2017

    Carriage House Creations; Bourbon Basting Sauce Mild; Net wt. 12 Ounces; Carriage House Creati...

    Carriage House Creations is recalling 3 varieties of Bourbon Basting Sauce and Hot BBQ Sauce due to undeclared peanuts and soy. The recall was initiat...

    Carriage House Creations · Reynoldsville, PA

    Where it was sold: PA

    Show details
    Product, as FDA describes it
    Carriage House Creations; Bourbon Basting Sauce Mild; Net wt. 12 Ounces; Carriage House Creations, 544 Gordon Alley; Reynoldsville, PA 15851;
    Reason, in FDA's words
    Carriage House Creations is recalling 3 varieties of Bourbon Basting Sauce and Hot BBQ Sauce due to undeclared peanuts and soy. The recall was initiated after receiving notification that the Worcestershire sauce ingredient was recalled for the undeclared allergens.
    Codes on the package
    Batch # 2491601, Best If Used By: 3052018; Batch # 2581605, Best If Used By: 3142018; Batch # 3281614, Best If Used By: 5232018;
    Where it was sold
    PA
    Amount recalled
    59 cases 12 bottles/case
    Status
    Ended Nov 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1668-2017
    View in FDA's recall database
  9. ENDEDClass II · ModerateRecalled Jan 23, 2017

    Carriage House Creations; Bold N' Spicy Bourbon Basting Sauce; Net wt. 12 Ounces; Carriage Hou...

    Carriage House Creations is recalling 3 varieties of Bourbon Basting Sauce and Hot BBQ Sauce due to undeclared peanuts and soy. The recall was initiat...

    Carriage House Creations · Reynoldsville, PA

    Where it was sold: PA

    Show details
    Product, as FDA describes it
    Carriage House Creations; Bold N' Spicy Bourbon Basting Sauce; Net wt. 12 Ounces; Carriage House Creations, 544 Gordon Alley; Reynoldsville, PA 15851;
    Reason, in FDA's words
    Carriage House Creations is recalling 3 varieties of Bourbon Basting Sauce and Hot BBQ Sauce due to undeclared peanuts and soy. The recall was initiated after receiving notification that the Worcestershire sauce ingredient was recalled for the undeclared allergens.
    Codes on the package
    Batch # 2361605 , Best If Used By: 2232018 ; Batch # 2411603 , Best If Used By: 2282018 ; Batch # 2491602 , Best If Used By: 3052018 ; Batch # 2491604 , Best If Used By: 3052018 ; Batch # 2511602 , Best If Used By: 3072018 ; Batch # 2711602 , Best If Used By: 3272018 ; Batch # 2711604 , Best If Used By: 3272018 ; Batch # 2711605 , Best If Used By: 3272018 ; Batch # 2791604 , Best If Used By: 4052018 ; Batch # 2791605 , Best If Used By: 4052018 ; Batch # 2801601 , Best If Used By: 4052018 ; Batch # 2881604 , Best If Used By: 4142018 ; Batch # 3011602 , Best If Used By: 4272018 ; Batch # 3191603 , Best If Used By: 5142018 ; Batch # 3191607 , Best If Used By: 5152018 ; Batch # 3241601 , Best If Used By: 5192018 ; Batch # 3241603 , Best If Used By: 5192018 ; Batch # 3051603 , Best If Used By: 5302018 ;
    Where it was sold
    PA
    Amount recalled
    489 cases 12 bottles/case
    Status
    Ended Nov 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1669-2017
    View in FDA's recall database
  10. ENDEDClass II · ModerateRecalled Jan 23, 2017

    Carriage House Creations; Bourbon Basting Sauce Hot; Net wt. 12 Ounces; Carriage House Creatio...

    Carriage House Creations is recalling 3 varieties of Bourbon Basting Sauce and Hot BBQ Sauce due to undeclared peanuts and soy. The recall was initiat...

    Carriage House Creations · Reynoldsville, PA

    Where it was sold: PA

    Show details
    Product, as FDA describes it
    Carriage House Creations; Bourbon Basting Sauce Hot; Net wt. 12 Ounces; Carriage House Creations, 544 Gordon Alley; Reynoldsville, PA 15851;
    Reason, in FDA's words
    Carriage House Creations is recalling 3 varieties of Bourbon Basting Sauce and Hot BBQ Sauce due to undeclared peanuts and soy. The recall was initiated after receiving notification that the Worcestershire sauce ingredient was recalled for the undeclared allergens.
    Codes on the package
    Batch # 2481602 , Best If Used By: 3042018 ; Batch # 2511603 , Best If Used By: 3072018 ; Batch # 2701605 , Best If Used By: 3262018 ; Batch # 3011604 , Best If Used By: 4272018 ;
    Where it was sold
    PA
    Amount recalled
    92 cases, 12 bottles/cs
    Status
    Ended Nov 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1670-2017
    View in FDA's recall database
  11. ENDEDClass I · Most seriousRecalled Jan 22, 2017

    Trader Joe's Harvest Whole Wheat Bread; NET WT 24 oz. (1 lb. 8 oz.) SKU 00132; UPC: 0000 1328. ...

    Certain production dates of Trader Joe's Harvest Whole Wheat Bread do not declare cultured whey or list milk as an allergen.

    Athens Baking Company · Fresno, CA

    Where it was sold: AZ, CA, NV, NM, UT.

    Show details
    Product, as FDA describes it
    Trader Joe's Harvest Whole Wheat Bread; NET WT 24 oz. (1 lb. 8 oz.) SKU 00132; UPC: 0000 1328. Distributed and sold exclusively by: Trader Joe's, Monrovia, CA 91016
    Reason, in FDA's words
    Certain production dates of Trader Joe's Harvest Whole Wheat Bread do not declare cultured whey or list milk as an allergen.
    Codes on the package
    Best by Dates: 1/08/2017 through 1-27-2017. Code numbers: 364, 002, 004,005,006,010, 012,013,017.
    Where it was sold
    AZ, CA, NV, NM, UT.
    Amount recalled
    76410 units
    Status
    Ended Mar 30, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1525-2017
    View in FDA's recall database
  12. ENDEDClass II · ModerateRecalled Jan 20, 2017

    Fresh Foods Market Delicatessen Rotini Pasta Salad; Net Wt. 10 oz . (283g) Clamshell package. U...

    Retail store employee found that 10 oz. containers of Rotini Salad had the ingredient label for mustard potato salad; thus the allergen of wheat is no...

    Taylor Farms Pacific, Inc. · Tracy, CA

    Where it was sold: TN, MS, MO, AR, KY

    Show details
    Product, as FDA describes it
    Fresh Foods Market Delicatessen Rotini Pasta Salad; Net Wt. 10 oz . (283g) Clamshell package. UPC Code: WO2017019 Perishable; Keep Refrigerated; Distributed by The Kroger Col., Cincinnati, OH
    Reason, in FDA's words
    Retail store employee found that 10 oz. containers of Rotini Salad had the ingredient label for mustard potato salad; thus the allergen of wheat is not declared.
    Codes on the package
    62180-01; TFTN 019 Sell by: 01/24/2017; Batch number: WO2017019
    Where it was sold
    TN, MS, MO, AR, KY
    Amount recalled
    81 x 10 oz. clam shell packages
    Status
    Ended Apr 3, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1452-2017
    View in FDA's recall database
  13. ENDEDClass II · ModerateRecalled Jan 20, 2017

    Specialty Commodities, Inc., Almond, Dry RNS, SKU 0020034064 Item number ALMO-033, 25 lb carton.

    One lot of dry roasted almonds may contain undeclared cashews.

    Archer Daniels Midland Company · Decatur, IL

    Where it was sold: CA

    Show details
    Product, as FDA describes it
    Specialty Commodities, Inc., Almond, Dry RNS, SKU 0020034064 Item number ALMO-033, 25 lb carton.
    Reason, in FDA's words
    One lot of dry roasted almonds may contain undeclared cashews.
    Codes on the package
    Manufacturer lot number 1050188-1-16007
    Where it was sold
    CA
    Amount recalled
    3,525 lbs
    Status
    Ended Aug 2, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1523-2017
    View in FDA's recall database
  14. ENDEDClass II · ModerateRecalled Jan 12, 2017

    Los Chileros, Basil Pesto, Net Wt. 6 oz. (170g). plastic shell container. Keep Refrigerated

    Basil Pesto ingredient list did not list "milk" after the ingredient Parmesan Cheese.

    Los Chileros De Nuevo Mexico, LLC · Albuquerque, NM

    Where it was sold: Retail stores in NM

    Show details
    Product, as FDA describes it
    Los Chileros, Basil Pesto, Net Wt. 6 oz. (170g). plastic shell container. Keep Refrigerated
    Reason, in FDA's words
    Basil Pesto ingredient list did not list "milk" after the ingredient Parmesan Cheese.
    Codes on the package
    Lots 012017, 021017, 022417, 032217, 040517
    Where it was sold
    Retail stores in NM
    Amount recalled
    848 units
    Status
    Ended Dec 20, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1386-2017
    View in FDA's recall database
  15. ENDEDClass I · Most seriousRecalled Jan 11, 2017

    Golden Flake (R) HOT THIN & CRISPY POTATO CHIPS, NET WT. 5 OZ. (141.8g), Golden Flake Snack Foods, I...

    undeclared milk

    Golden Flake Snack Foods Inc · Birmingham, AL

    Where it was sold: AL, AR, FL, GA, IN, KY, LA, MO, MS, NC, SC, TN, TX, VA

    UPC 072080002403
    Show details
    Product, as FDA describes it
    Golden Flake (R) HOT THIN & CRISPY POTATO CHIPS, NET WT. 5 OZ. (141.8g), Golden Flake Snack Foods, Inc., Birmingham, AL 35201, UPC 0-72080-00240-3
    Reason, in FDA's words
    undeclared milk
    Codes on the package
    Lot Numbers: APR1417 364 5 and APR1417 365 5
    Where it was sold
    AL, AR, FL, GA, IN, KY, LA, MO, MS, NC, SC, TN, TX, VA
    Amount recalled
    1743/16 unit cases
    Status
    Ended Jul 5, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1526-2017
    View in FDA's recall database
  16. ENDEDClass II · ModerateRecalled Jan 11, 2017

    Gift Sets with Pretzel Twists

    The product is not labeled with an ingredient statement and therefore, does not declare the allergens, soy and wheat.

    Robert Rothschild Farm LLC · Urbana, OH

    Where it was sold: This product was distributed nationwide. Product was distributed in Canada.

    Show details
    Product, as FDA describes it
    Gift Sets with Pretzel Twists
    Reason, in FDA's words
    The product is not labeled with an ingredient statement and therefore, does not declare the allergens, soy and wheat.
    Codes on the package
    98016 - Use by date 9/21/16 through 9/06/17
    Where it was sold
    This product was distributed nationwide. Product was distributed in Canada.
    Amount recalled
    126,419 Units
    Status
    Ended Jan 31, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1574-2017
    View in FDA's recall database
  17. ENDEDClass II · ModerateRecalled Jan 11, 2017

    Gift Sets with Chocolate Pretzel Dippers

    The product is not labeled with an ingredient statement and therefore, does not declare the allergens, soy and wheat.

    Robert Rothschild Farm LLC · Urbana, OH

    Where it was sold: This product was distributed nationwide. Product was distributed in Canada.

    Show details
    Product, as FDA describes it
    Gift Sets with Chocolate Pretzel Dippers
    Reason, in FDA's words
    The product is not labeled with an ingredient statement and therefore, does not declare the allergens, soy and wheat.
    Codes on the package
    88035 - Use by dates 1/21/16 thorugh 3/14/17
    Where it was sold
    This product was distributed nationwide. Product was distributed in Canada.
    Amount recalled
    28,288 units
    Status
    Ended Jan 31, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1575-2017
    View in FDA's recall database
  18. ENDEDClass I · Most seriousRecalled Jan 10, 2017

    Snacking Favorites Organic Veggies with Organic Ranch Dip. 16.25 oz. plastic tray (1.02 lb.) ...

    Mann Packing was notified by a customer that the incorrect bottom label is on their Organic Veggie Tray with Best By date of January 14, 2017 and does...

    Mann Packing Company, Inc. · Salinas, CA

    Where it was sold: MN, NY, FL, IA, TX.

    UPC 716519014710UPC 716519014765
    Show details
    Product, as FDA describes it
    Snacking Favorites Organic Veggies with Organic Ranch Dip. 16.25 oz. plastic tray (1.02 lb.) UPC barcode: 71651901471 - this is the incorrect barcode that is on the bottom of recalled product. Correct UPC: 716519014765 Incorrect Allergen Statement: Egg. Milk Correct Allergen Statement, Egg, Milk, Soy and Mustard.
    Reason, in FDA's words
    Mann Packing was notified by a customer that the incorrect bottom label is on their Organic Veggie Tray with Best By date of January 14, 2017 and does not declare the allergens of egg, milk, soy and mustard.
    Codes on the package
    Best if Used by: January 14, 2017; Lot Serial # 3658366
    Where it was sold
    MN, NY, FL, IA, TX.
    Amount recalled
    201 cases (4 trays per case)
    Status
    Ended Feb 15, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1432-2017
    View in FDA's recall database
  19. ENDEDClass I · Most seriousRecalled Jan 10, 2017

    DARK CRUNCH Chip 'n Dipped Chocolatier DARK CHOCOLATE CRUNCH, NET WT. 2.9oz 82g, UPC 892470002246

    Presence of Undeclared Milk Allergen

    Chip'n Dipped · Huntington, NY

    Where it was sold: Ten (10) retail store chains in NY, PA and MA

    UPC 892470002246
    Show details
    Product, as FDA describes it
    DARK CRUNCH Chip 'n Dipped Chocolatier DARK CHOCOLATE CRUNCH, NET WT. 2.9oz 82g, UPC 892470002246
    Reason, in FDA's words
    Presence of Undeclared Milk Allergen
    Codes on the package
    Lot# 1100524, 100506 and 1100483 are stamped on the back of the packaging box, individual units are unmarked.
    Where it was sold
    Ten (10) retail store chains in NY, PA and MA
    Amount recalled
    30 boxes/12bars
    Status
    Ended Jun 25, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1515-2017
    View in FDA's recall database
  20. ENDEDClass I · Most seriousRecalled Jan 10, 2017

    63% CACAO DARK Chip 'n Dipped Chocolatier 63% CACAO DARK CHOCOLATE, NET WT. 2.9oz 82g, UPC 892470002...

    Presence of Undeclared Milk Allergen

    Chip'n Dipped · Huntington, NY

    Where it was sold: Ten (10) retail store chains in NY, PA and MA

    UPC 892470002161
    Show details
    Product, as FDA describes it
    63% CACAO DARK Chip 'n Dipped Chocolatier 63% CACAO DARK CHOCOLATE, NET WT. 2.9oz 82g, UPC 892470002161
    Reason, in FDA's words
    Presence of Undeclared Milk Allergen
    Codes on the package
    Lot# 1100501 & 1100536 are stamped on the back of the packaging box, individual units are unmarked.
    Where it was sold
    Ten (10) retail store chains in NY, PA and MA
    Amount recalled
    8 boxes/16 units
    Status
    Ended Jun 25, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1516-2017
    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.