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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

Recall News: the highest-risk recalls, explained

7,366 ended recalls · showing 6,881 to 6,900

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  1. ENDEDClass I · Most seriousRecalled Feb 5, 2013

    BUFFALO TRACE ORIGINAL FLAVOR BARBEQUE SAUCE Net Wt. 16 fl. oz./532 ml PRODUCED BY: APPLECREEK ORCHA...

    The firm failed to include allergens of soy and anchovy on the label of this sauce.

    Buffalo Trace Distillery · Frankfort, KY

    Where it was sold: Product was distributed to the following states: AL, AZ, CA, CO, GA, IL, IN, KS, KY, LA, MD, MI, MO, NC, NE, NJ, NV, NY, OK, PA, SD, TN, TX, VA, WA, WI & WV. Product was also ship...

    UPC 795436001065
    Show details
    Product, as FDA describes it
    BUFFALO TRACE ORIGINAL FLAVOR BARBEQUE SAUCE Net Wt. 16 fl. oz./532 ml PRODUCED BY: APPLECREEK ORCHARDS LLC P.O. Box 8383 Lexington, KY 40533 BUFFALO TRACE DISTILLERY 113 Great Buffalo Trace Franklin County Frankfort, KY 40601 800-654-8471 e-mail: greatboubon@buffalotrace.com website: www.buffalotrace.com UPC 7 95436 00106 5 Best By 1/19/15
    Reason, in FDA's words
    The firm failed to include allergens of soy and anchovy on the label of this sauce.
    Codes on the package
    Best By 1/19/15
    Where it was sold
    Product was distributed to the following states: AL, AZ, CA, CO, GA, IL, IN, KS, KY, LA, MD, MI, MO, NC, NE, NJ, NV, NY, OK, PA, SD, TN, TX, VA, WA, WI & WV. Product was also shipped to Canada and the United Kingdom.
    Amount recalled
    1,658/16 fl. oz. jar
    Status
    Ended Dec 2, 2013 (FDA lists it as terminated)
    FDA recall number
    F-1375-2013
    View in FDA's recall database
  2. ENDEDClass I · Most seriousRecalled Feb 5, 2013

    BUFFALO TRACE HOT BARBEQUE SAUCE Net Wt. 16 fl. oz./532 ml PRODUCED BY: APPLECREEK ORCHARDS LLC P.O....

    The firm failed to include allergens of soy and anchovy on the labels of this sauce.

    Buffalo Trace Distillery · Frankfort, KY

    Where it was sold: Product was distributed to the following states: AL, AZ, CA, CO, GA, IL, IN, KS, KY, LA, MD, MI, MO, NC, NE, NJ, NV, NY, OK, PA, SD, TN, TX, VA, WA, WI & WV. Product was also ship...

    UPC 795436000174
    Show details
    Product, as FDA describes it
    BUFFALO TRACE HOT BARBEQUE SAUCE Net Wt. 16 fl. oz./532 ml PRODUCED BY: APPLECREEK ORCHARDS LLC P.O. Box 8383 Lexington, KY 40533 BUFFALO TRACE DISTILLERY 113 Great Buffalo Trace Franklin County Frankfort, KY 40601 800-654-8471 e-mail: greatboubon@buffalotrace.com website: www.buffalotrace.com UPC 7 95436 00017 4 Best By 11/7/14
    Reason, in FDA's words
    The firm failed to include allergens of soy and anchovy on the labels of this sauce.
    Codes on the package
    Best By 11/7/14
    Where it was sold
    Product was distributed to the following states: AL, AZ, CA, CO, GA, IL, IN, KS, KY, LA, MD, MI, MO, NC, NE, NJ, NV, NY, OK, PA, SD, TN, TX, VA, WA, WI & WV. Product was also shipped to Canada and the United Kingdom.
    Amount recalled
    635/16 fl. oz. jars
    Status
    Ended Dec 2, 2013 (FDA lists it as terminated)
    FDA recall number
    F-1376-2013
    View in FDA's recall database
  3. ENDEDClass II · ModerateRecalled Jan 30, 2013

    Z Pro 25 High Protein Supplement Net. Wt. 1.3 oz. - Vanilla Flavor Formulated and Distributed...

    Z Pro High Protein Vanilla Flavor Supplement is under recall because it contains the allergens milk and coconut, a tree nut, which are not declared on...

    R-Kane Products Inc. · Pennsauken, NJ

    Where it was sold: Nationwide

    Show details
    Product, as FDA describes it
    Z Pro 25 High Protein Supplement Net. Wt. 1.3 oz. - Vanilla Flavor Formulated and Distributed by: R-Kane Products, Inc. 8351 National Highway, Pennsauken, NJ 08110
    Reason, in FDA's words
    Z Pro High Protein Vanilla Flavor Supplement is under recall because it contains the allergens milk and coconut, a tree nut, which are not declared on the label of the individual packets of the product.
    Codes on the package
    All codes distributed between 1/1/2011 and 1/24/2013
    Where it was sold
    Nationwide
    Amount recalled
    unavailable
    Status
    Ended Jul 15, 2015 (FDA lists it as terminated)
    FDA recall number
    F-1056-2013
    View in FDA's recall database
  4. ENDEDClass II · ModerateRecalled Jan 30, 2013

    Z Pro 25 High Protein Supplement Net. Wt. 1.5 oz. - Chocolate Flavor Formulated and Distribu...

    Z Pro High Protein Chocolate Flavor Supplement is under recall since it contains milk and soy, allergens, which are not declared on the label of the i...

    R-Kane Products Inc. · Pennsauken, NJ

    Where it was sold: Nationwide

    Show details
    Product, as FDA describes it
    Z Pro 25 High Protein Supplement Net. Wt. 1.5 oz. - Chocolate Flavor Formulated and Distributed by: R-Kane Products, Inc. 8351 National Highway, Pennsauken, NJ 08110
    Reason, in FDA's words
    Z Pro High Protein Chocolate Flavor Supplement is under recall since it contains milk and soy, allergens, which are not declared on the label of the individual packets of the product.
    Codes on the package
    All codes distributed between 1/1/2011 and 1/24/2013
    Where it was sold
    Nationwide
    Amount recalled
    N/A
    Status
    Ended Jul 15, 2015 (FDA lists it as terminated)
    FDA recall number
    F-1057-2013
    View in FDA's recall database
  5. ENDEDClass I · Most seriousRecalled Jan 28, 2013

    Labeled in part: "All Natural Chia ReCharged Stix Mix***Chia Seed Sticks***Net Wt. 5oz", UPC Code: 0...

    Undeclared peanuts.

    Tropical Nut & Fruit Co., Inc. · Orlando, FL

    Where it was sold: Distribution Pattern: FL and NC

    UPC 094184010146
    Show details
    Product, as FDA describes it
    Labeled in part: "All Natural Chia ReCharged Stix Mix***Chia Seed Sticks***Net Wt. 5oz", UPC Code: 0 94184 01014 6
    Reason, in FDA's words
    Undeclared peanuts.
    Codes on the package
    Lot #'s: 052112, 060512, 071712, 080212, and 081612; Best Before dates 01/20/13 to 04/17/13
    Where it was sold
    Distribution Pattern: FL and NC
    Amount recalled
    1,380 lbs
    Status
    Ended Mar 27, 2013 (FDA lists it as terminated)
    FDA recall number
    F-0990-2013
    View in FDA's recall database
  6. ENDEDClass I · Most seriousRecalled Jan 17, 2013

    Kinnikinnick Pie Crust (frozen), Weight: 290 g/10 oz, Qty/Pkg: 2, Product packaged in a cardboard bo...

    Kinnikinnick Foods, Inc. in Edmonton, Alberta Canada indicated that United Natural Foods Inc. distributors received pie crusts in association with the...

    United Natural Foods, Inc. - Greenwood · Greenwood, IN

    Where it was sold: Customers are retail locations in 6 states: Illinois, Indiana, Kentucky, Michigan, Missouri, and Ohio.

    UPC 620133006009
    Show details
    Product, as FDA describes it
    Kinnikinnick Pie Crust (frozen), Weight: 290 g/10 oz, Qty/Pkg: 2, Product packaged in a cardboard box with printed label. UPC: 62013300600 9
    Reason, in FDA's words
    Kinnikinnick Foods, Inc. in Edmonton, Alberta Canada indicated that United Natural Foods Inc. distributors received pie crusts in association with their expanded recall/allergy alert issued 01/17/13.
    Codes on the package
    Expiration date 2013-12-11
    Where it was sold
    Customers are retail locations in 6 states: Illinois, Indiana, Kentucky, Michigan, Missouri, and Ohio.
    Amount recalled
    28 cases/6 packages per case
    Status
    Ended Sep 30, 2013 (FDA lists it as terminated)
    FDA recall number
    F-0960-2013
    View in FDA's recall database
  7. ENDEDClass I · Most seriousRecalled Jan 15, 2013

    DYMATIZE NUTRITION ELITE Gourmet Cookies & Cream 6-LAYER HI-PROTEIN BAR Label reads in part "NET WT*...

    Belmont was notified by their customer, Dymatize, that a consumer complained on an allergic reaction after eating the product. The consumer is allerg...

    Belmont Confections Inc · Youngstown, OH

    Where it was sold: Product was shipped to the following state: Texas

    Show details
    Product, as FDA describes it
    DYMATIZE NUTRITION ELITE Gourmet Cookies & Cream 6-LAYER HI-PROTEIN BAR Label reads in part "NET WT***INGREDIENTS: Elite Protein Blend***Distributed by: Dymatize Enterprises, Inc. 13737 N. Stemmons FWY, Dallas, TX 75234, (888) 334-LEAN or (972) 732-1990.
    Reason, in FDA's words
    Belmont was notified by their customer, Dymatize, that a consumer complained on an allergic reaction after eating the product. The consumer is allergic to peanuts & peanut protein.
    Codes on the package
    Dymatize Nutrition Elite Gourmet Cookies & Cream 1.5oz (42.5g), UPC Code, 705016993147, Lot # 12200A, Best By Date SEP 2013, Lot # 12249A, Best By Date NOV 2013, Lot # 12310A, Best By Date JAN 2014 & Lot # 12353A, Best By Date FEB 2014. Dymatize Nutrition Elite Gourmet Cookies & Cream 3oz (85g), UPC Code, 705016993000, Lot #, 12072A, Best By Date MAY 2013, Lot # 12200A, Best By Date SEP 2013, Lot # 12310A, Best By Date JAN 2014 & Lot # 12353A, Best By Date FEB 2014.
    Where it was sold
    Product was shipped to the following state: Texas
    Amount recalled
    195,552/3 oz bars & 73,296/1.5 oz bars
    Status
    Ended Oct 13, 2015 (FDA lists it as terminated)
    FDA recall number
    F-0963-2013
    View in FDA's recall database
  8. ENDEDClass I · Most seriousRecalled Jan 15, 2013

    DYMATIZE NUTRITION ELITE Gourmet Fudge Brownie 6-LAYER HI-PROTEIN BAR Label reads in part "NET WT***...

    Belmont was notified by their customer, Dymatize, that a consumer complained on an allergic reaction after eating the product. The consumer is allerg...

    Belmont Confections Inc · Youngstown, OH

    Where it was sold: Product was shipped to the following state: Texas

    Show details
    Product, as FDA describes it
    DYMATIZE NUTRITION ELITE Gourmet Fudge Brownie 6-LAYER HI-PROTEIN BAR Label reads in part "NET WT***INGREDIENTS: Elite Protein Blend***Distributed by: Dymatize Enterprises, Inc. 13737 N. Stemmons FWY, Dallas, TX 75234, (888) 334-LEAN or (972) 732-1990.
    Reason, in FDA's words
    Belmont was notified by their customer, Dymatize, that a consumer complained on an allergic reaction after eating the product. The consumer is allergic to peanuts & peanut protein.
    Codes on the package
    Dymatize Nutrition Elite Gourmet Fudge Brownie 1.5oz (42.5g), UPC Code, 705016993130, Lot #, 12199A, Best By Date SEP 2013, Lot # 12244A, Best By Date OCT 2013, Lot # 12311B, Best By Date JAN 2014 & Lot # 12352B, Best By Date FEB 2014. Dymatize Nutrition Elite Gourmet Fudge Brownie 3oz (85g), UPC Code, 705016993079, Lot #, 12084A, Best By Date MAY 2013, Lot # 12199A, Best By Date SEP 2013, Lot # 12205A, Best By Date SEP 2013, Lot # 12311B, Best By Date JAN 2014 & Lot # 12352B, Best By Date FEB 2014.
    Where it was sold
    Product was shipped to the following state: Texas
    Amount recalled
    152,280/3 oz bars & 67,536/1,5 oz bars
    Status
    Ended Oct 13, 2015 (FDA lists it as terminated)
    FDA recall number
    F-0964-2013
    View in FDA's recall database
  9. ENDEDClass I · Most seriousRecalled Jan 11, 2013

    Spice Cake Mix , 25 lb. and 50 lb. kraft bags, labelled a) CMC Quality and Value, Spice Cake Mix, 46...

    Undeclared Allergen (Milk). Firm initiated a voluntary recall of their 25 lb. and 50 lb. bags of Spice Cake Mix that had been distributed since Augus...

    Jiffy Food Service, LLC · Chelsea, MI

    Where it was sold: Nationwide including Arizona, California, Colorado, Connecicut, Florida, Georgia, Idaho, Illinois, Kentucky, Louisiana, Michigan, Missouri, Montana, New England, New Jersey, New Me...

    UPC 846702009855
    Show details
    Product, as FDA describes it
    Spice Cake Mix , 25 lb. and 50 lb. kraft bags, labelled a) CMC Quality and Value, Spice Cake Mix, 46702-00985, NET Wt. 25 lbs. (11.34 kg) JIFFY Foodservice, LLC, Chelsea, Michigan 48188; b) CMC Quality and Value, Spice Cake Mix, 46702-00920, NET Wt. 50 lbs. (22.68 kg.), JIFFY Foodservice, LLC, Chelsea, Michigan 48188.
    Reason, in FDA's words
    Undeclared Allergen (Milk). Firm initiated a voluntary recall of their 25 lb. and 50 lb. bags of Spice Cake Mix that had been distributed since August 2012 due to an undeclared allergen, milk. The Spice Cake Mix is manufactured for correctional facilities/institutions only.
    Codes on the package
    UPC Code 84670200985 Manufacturing Date Codes (printed on the inside seam/gusset of the bag): 08/01/2012, 08/23/2012, 10/03/2012, 11/18/2012, 11/19/2012.
    Where it was sold
    Nationwide including Arizona, California, Colorado, Connecicut, Florida, Georgia, Idaho, Illinois, Kentucky, Louisiana, Michigan, Missouri, Montana, New England, New Jersey, New Mexico, Nevada, Oklahoma, Pennsylvania, South Dakota, Tennessee, Texas, Utah, Virgina and Wisconsin.
    Amount recalled
    7,422 bags (total 25 lb. and 50 lb. combined)
    Status
    Ended Jul 12, 2013 (FDA lists it as terminated)
    FDA recall number
    F-0941-2013
    View in FDA's recall database
  10. ENDEDClass II · ModerateRecalled Jan 9, 2013

    Foil bags containing 2.2 lbs. each of almond flavored powder and sold under the Boba Direct, Inc. br...

    Bubble tea powders contain undeclared allergens.

    Boba Direct, Inc. · Mundelein, IL

    Where it was sold: US: IL, MO, OH, FL, and TN

    Show details
    Product, as FDA describes it
    Foil bags containing 2.2 lbs. each of almond flavored powder and sold under the Boba Direct, Inc. brand.
    Reason, in FDA's words
    Bubble tea powders contain undeclared allergens.
    Codes on the package
    Product code: AlmndPwdr-BD; All lots
    Where it was sold
    US: IL, MO, OH, FL, and TN
    Amount recalled
    N/A
    Status
    Ended Aug 14, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2791-2015
    View in FDA's recall database
  11. ENDEDClass II · ModerateRecalled Jan 9, 2013

    Foil bags containing 2.2 lbs. each of avocado flavored powder and sold under the Boba Direct, Inc. b...

    Bubble tea powders contain undeclared allergens.

    Boba Direct, Inc. · Mundelein, IL

    Where it was sold: US: IL, MO, OH, FL, and TN

    Show details
    Product, as FDA describes it
    Foil bags containing 2.2 lbs. each of avocado flavored powder and sold under the Boba Direct, Inc. brand.
    Reason, in FDA's words
    Bubble tea powders contain undeclared allergens.
    Codes on the package
    Product code: AvoPwdr-BD; All lots
    Where it was sold
    US: IL, MO, OH, FL, and TN
    Amount recalled
    N/A
    Status
    Ended Aug 14, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2792-2015
    View in FDA's recall database
  12. ENDEDClass II · ModerateRecalled Jan 9, 2013

    Foil bags containing 2.2 lbs. each of banana flavored powder and sold under the Boba Direct, Inc. br...

    Bubble tea powders contain undeclared allergens.

    Boba Direct, Inc. · Mundelein, IL

    Where it was sold: US: IL, MO, OH, FL, and TN

    Show details
    Product, as FDA describes it
    Foil bags containing 2.2 lbs. each of banana flavored powder and sold under the Boba Direct, Inc. brand.
    Reason, in FDA's words
    Bubble tea powders contain undeclared allergens.
    Codes on the package
    Product code: BanaPwdr-BD; All lots
    Where it was sold
    US: IL, MO, OH, FL, and TN
    Amount recalled
    N/A
    Status
    Ended Aug 14, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2793-2015
    View in FDA's recall database
  13. ENDEDClass II · ModerateRecalled Jan 9, 2013

    Foil bags containing 2.2 lbs. each of blueberry flavored powder and sold under the Boba Direct, Inc....

    Bubble tea powders contain undeclared allergens.

    Boba Direct, Inc. · Mundelein, IL

    Where it was sold: US: IL, MO, OH, FL, and TN

    Show details
    Product, as FDA describes it
    Foil bags containing 2.2 lbs. each of blueberry flavored powder and sold under the Boba Direct, Inc. brand.
    Reason, in FDA's words
    Bubble tea powders contain undeclared allergens.
    Codes on the package
    Product code: BlueberryPwdr-BD; All lots
    Where it was sold
    US: IL, MO, OH, FL, and TN
    Amount recalled
    N/A
    Status
    Ended Aug 14, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2794-2015
    View in FDA's recall database
  14. ENDEDClass II · ModerateRecalled Jan 9, 2013

    Foil bags containing 2.2 lbs. each of cafe latte flavored powder and sold under the Boba Direct, Inc...

    Bubble tea powders contain undeclared allergens.

    Boba Direct, Inc. · Mundelein, IL

    Where it was sold: US: IL, MO, OH, FL, and TN

    Show details
    Product, as FDA describes it
    Foil bags containing 2.2 lbs. each of cafe latte flavored powder and sold under the Boba Direct, Inc. brand.
    Reason, in FDA's words
    Bubble tea powders contain undeclared allergens.
    Codes on the package
    Product code: CafelattePwdr-BD; All lots
    Where it was sold
    US: IL, MO, OH, FL, and TN
    Amount recalled
    N/A
    Status
    Ended Aug 14, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2795-2015
    View in FDA's recall database
  15. ENDEDClass II · ModerateRecalled Jan 9, 2013

    Foil bags containing 2.2 lbs. each of cherry flavored powder and sold under the Boba Direct, Inc. br...

    Bubble tea powders contain undeclared allergens.

    Boba Direct, Inc. · Mundelein, IL

    Where it was sold: US: IL, MO, OH, FL, and TN

    Show details
    Product, as FDA describes it
    Foil bags containing 2.2 lbs. each of cherry flavored powder and sold under the Boba Direct, Inc. brand.
    Reason, in FDA's words
    Bubble tea powders contain undeclared allergens.
    Codes on the package
    Product code: CherryPwdr-BD; All lots
    Where it was sold
    US: IL, MO, OH, FL, and TN
    Amount recalled
    N/A
    Status
    Ended Aug 14, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2796-2015
    View in FDA's recall database
  16. ENDEDClass II · ModerateRecalled Jan 9, 2013

    Foil bags containing 2.2 lbs. each of chocolate flavored powder and sold under the Boba Direct, Inc....

    Bubble tea powders contain undeclared allergens.

    Boba Direct, Inc. · Mundelein, IL

    Where it was sold: US: IL, MO, OH, FL, and TN

    Show details
    Product, as FDA describes it
    Foil bags containing 2.2 lbs. each of chocolate flavored powder and sold under the Boba Direct, Inc. brand.
    Reason, in FDA's words
    Bubble tea powders contain undeclared allergens.
    Codes on the package
    Product code: ChocPwdr-BD; All lots
    Where it was sold
    US: IL, MO, OH, FL, and TN
    Amount recalled
    N/A
    Status
    Ended Aug 14, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2797-2015
    View in FDA's recall database
  17. ENDEDClass II · ModerateRecalled Jan 9, 2013

    Foil bags containing 2.2 lbs. each of coconut flavored powder and sold under the Boba Direct, Inc. b...

    Bubble tea powders contain undeclared allergens.

    Boba Direct, Inc. · Mundelein, IL

    Where it was sold: US: IL, MO, OH, FL, and TN

    Show details
    Product, as FDA describes it
    Foil bags containing 2.2 lbs. each of coconut flavored powder and sold under the Boba Direct, Inc. brand.
    Reason, in FDA's words
    Bubble tea powders contain undeclared allergens.
    Codes on the package
    Product code: CoconutPwdr-BD; All lots
    Where it was sold
    US: IL, MO, OH, FL, and TN
    Amount recalled
    N/A
    Status
    Ended Aug 14, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2798-2015
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled Jan 9, 2013

    Foil bags containing 2.2 lbs. each of honeydew flavored powder and sold under the Boba Direct, Inc. ...

    Bubble tea powders contain undeclared allergens.

    Boba Direct, Inc. · Mundelein, IL

    Where it was sold: US: IL, MO, OH, FL, and TN

    Show details
    Product, as FDA describes it
    Foil bags containing 2.2 lbs. each of honeydew flavored powder and sold under the Boba Direct, Inc. brand.
    Reason, in FDA's words
    Bubble tea powders contain undeclared allergens.
    Codes on the package
    Product code: HnydewPwdr-BD; All lots
    Where it was sold
    US: IL, MO, OH, FL, and TN
    Amount recalled
    N/A
    Status
    Ended Aug 14, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2799-2015
    View in FDA's recall database
  19. ENDEDClass II · ModerateRecalled Jan 9, 2013

    Foil bags containing 2.2 lbs. each of lavender flavored powder and sold under the Boba Direct, Inc. ...

    Bubble tea powders contain undeclared allergens.

    Boba Direct, Inc. · Mundelein, IL

    Where it was sold: US: IL, MO, OH, FL, and TN

    Show details
    Product, as FDA describes it
    Foil bags containing 2.2 lbs. each of lavender flavored powder and sold under the Boba Direct, Inc. brand.
    Reason, in FDA's words
    Bubble tea powders contain undeclared allergens.
    Codes on the package
    Product code: LavPwdr-BD; All lots
    Where it was sold
    US: IL, MO, OH, FL, and TN
    Amount recalled
    N/A
    Status
    Ended Aug 14, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2800-2015
    View in FDA's recall database
  20. ENDEDClass II · ModerateRecalled Jan 9, 2013

    Foil bags containing 2.2 lbs. each of lychee flavored powder and sold under the Boba Direct, Inc. br...

    Bubble tea powders contain undeclared allergens.

    Boba Direct, Inc. · Mundelein, IL

    Where it was sold: US: IL, MO, OH, FL, and TN

    Show details
    Product, as FDA describes it
    Foil bags containing 2.2 lbs. each of lychee flavored powder and sold under the Boba Direct, Inc. brand.
    Reason, in FDA's words
    Bubble tea powders contain undeclared allergens.
    Codes on the package
    Product code: LycheePwdr-BD; All lots
    Where it was sold
    US: IL, MO, OH, FL, and TN
    Amount recalled
    N/A
    Status
    Ended Aug 14, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2801-2015
    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.

At the store?

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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.