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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 6,741 to 6,760

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  1. ENDEDClass I · Most seriousRecalled May 29, 2013

    Lightlife Farmer's Market Veggie Burgers, meat free, 12 oz/4-count bag, packaged in 5/12 oz-bag/cart...

    The product packaging for Lighthouse Farmer's Market Veggie Burgers may contain Lightlife Kick'n Black Bean Burgers which contain milk. The milk alle...

    Conagra Inc · Omaha, NE

    Where it was sold: Distribution was made to AL, AR, AZ, CO, DE,FL,GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, MS, NC, NE, NJ, NM, NY, OH, OK, PA, SC, TN, TX, VA, VT and WI. No foriegn or militar...

    UPC 20043454805252
    Show details
    Product, as FDA describes it
    Lightlife Farmer's Market Veggie Burgers, meat free, 12 oz/4-count bag, packaged in 5/12 oz-bag/cartons. Distributed By: Lightlife Foods, Turners Falls, MA. Case UPC Code: 20043454805252
    Reason, in FDA's words
    The product packaging for Lighthouse Farmer's Market Veggie Burgers may contain Lightlife Kick'n Black Bean Burgers which contain milk. The milk allergen is not declared on the Farmer's Market Veggie Burger product label.
    Codes on the package
    Lot Code: 5483220300 and 5483221700 Best if Used by Dates: JULY 16 2013 and JULY 30 2013.
    Where it was sold
    Distribution was made to AL, AR, AZ, CO, DE,FL,GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, MS, NC, NE, NJ, NM, NY, OH, OK, PA, SC, TN, TX, VA, VT and WI. No foriegn or military distribution was made.
    Amount recalled
    66805/12-oz/4-count package/cases
    Status
    Ended May 13, 2014 (FDA lists it as terminated)
    FDA recall number
    F-1533-2013
    View in FDA's recall database
  2. ENDEDClass II · ModerateRecalled May 29, 2013

    Wholly Immune Powder, Total Immune Nutrient Support; 300 gram (10.6 oz) and 900 gram ( 31.7 oz.) c...

    Allergy Research Group received word from their contract manufacturer, ABCO Laboratories, that two of their products have been manufactured with soy b...

    Allergy Research Group · Alameda, CA

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

    Where it was sold: Distributors, Wholesalers, healthcare providers and retail customers in the USA. Nutrilink in England and DeltaStar in the Netherlands are distributors in Europe.

    Show details
    Product, as FDA describes it
    Wholly Immune Powder, Total Immune Nutrient Support; 300 gram (10.6 oz) and 900 gram ( 31.7 oz.) containers. Also packaged as Complete Immune Powder and packed in 300 and 900 gram containers. Suggested use: As a dietary supplement, 1 level scoop one or two times daily, mixed with desired liquid or as directed by a healthcare practitioner. California Proposition 65 warning: this product contains lead, a chemical known to the State of California to cause birth defects or other reproductive harm. UCP 13947-73560 and 13947 73820 formulated exclusively for Allergy Research Group, Alameda, CA 94502.
    Reason, in FDA's words
    Allergy Research Group received word from their contract manufacturer, ABCO Laboratories, that two of their products have been manufactured with soy based products from CHS Inc. at it Ashdod, Israel facility.
    Codes on the package
    Product number 73560, 53560 - 300 gr. Lot numbers: 11030685, Exp 6/1/13; 11030686, Exp 6/1/13; 11100829, Exp 11/1/13; 11100835, Exp 11/1/13; 12010362, Exp 4/1/14; 12061214, Exp 8/1/14; 12061217, Exp 8/1/14; 13010635, Exp. 2/1/15. Product number 73820, 53820 - 900 gr. Lot numbers: 11030676, Exp Jun 2013; 11030686, Exp 6/1/13; 11100836, Exp 11/1/13; 12010363, Exp 4/25/14; 12061215, Exp 8/1/14; 12061218, Exp 8/1/14; 13010636, Exp 2/1/15;
    Where it was sold
    Distributors, Wholesalers, healthcare providers and retail customers in the USA. Nutrilink in England and DeltaStar in the Netherlands are distributors in Europe.
    Amount recalled
    3000 units of 300 gr powder bottles' 1869 units of 900 gr bottles
    Status
    Ended Aug 28, 2013 (FDA lists it as terminated)
    FDA recall number
    F-1636-2013
    View in FDA's recall database
  3. ENDEDClass I · Most seriousRecalled May 24, 2013

    Blessing Brand Wild White EZ Peel Shrimp, 16/20 CT. 4 x 5 lbs cartons. The product is bagged in 5...

    Blessing Seafood, Inc. is voluntarily recalling one lot of Blessing Inc. Wild White EZ Peel Shrimp due to undeclared sulfites.

    Blessing Seafood, Inc. · Tucson, AZ

    Where it was sold: The 16-20 EZ Peel Shrimp was distributed by Perishable Distributors of Iowa (PDI) and sold from February 12 to May 23, 2013 at the seafood display counters in the retail markets se...

    Show details
    Product, as FDA describes it
    Blessing Brand Wild White EZ Peel Shrimp, 16/20 CT. 4 x 5 lbs cartons. The product is bagged in 5 lbs clear plastic bags, the only label iss on the master carton. The product is sold in a seafood retail case. Product labeled as:"WILD WHITE EZ PEEL SHRIMP 16/20 CT WILD CAUGHT PRODUCT OF USA CHEM FREE INGREDIENTS: Shrimp, Salt***PACKED BY: BLESSINGS, INC.***.
    Reason, in FDA's words
    Blessing Seafood, Inc. is voluntarily recalling one lot of Blessing Inc. Wild White EZ Peel Shrimp due to undeclared sulfites.
    Codes on the package
    Lot # 13047-1, 13048-1, and 13048-3
    Where it was sold
    The 16-20 EZ Peel Shrimp was distributed by Perishable Distributors of Iowa (PDI) and sold from February 12 to May 23, 2013 at the seafood display counters in the retail markets seafood section of Hy-Vee stores located in eight states: Iowa, Nebraska, Kansas, Illinois, Missouri, South Dakota, Minnesota, and Wisconsin, and at Cedar Valley Fish Market in Waterloo, Iowa.
    Amount recalled
    36,920 lbs
    Status
    Ended Jul 30, 2013 (FDA lists it as terminated)
    FDA recall number
    F-1528-2013
    View in FDA's recall database
  4. ENDEDClass I · Most seriousRecalled May 18, 2013

    White Farm Enriched White Bread. 16 oz (454g), 9pc/box. UPC 0 10314 10002 0. The label is white ...

    LL Bakery Inc. of Torrance, CA is recalling all White Farm Enriched White Bread, Butter Farm Enriched White Bread, and Italian Cream Danish because pr...

    LL Bakery, Inc. · Torrance, CA

    Where it was sold: HI, WA, and CA

    UPC 010314100020
    Show details
    Product, as FDA describes it
    White Farm Enriched White Bread. 16 oz (454g), 9pc/box. UPC 0 10314 10002 0. The label is white with blue and green lettering and red design accents. The LL Bakery Logo is on the bottom left corner.
    Reason, in FDA's words
    LL Bakery Inc. of Torrance, CA is recalling all White Farm Enriched White Bread, Butter Farm Enriched White Bread, and Italian Cream Danish because product labels fail to declare the allergen milk, in the whey powder listed in their ingredient statements.
    Codes on the package
    no lot codes
    Where it was sold
    HI, WA, and CA
    Amount recalled
    1020 units
    Status
    Ended Sep 25, 2013 (FDA lists it as terminated)
    FDA recall number
    F-1474-2013
    View in FDA's recall database
  5. ENDEDClass I · Most seriousRecalled May 18, 2013

    Butter Farm Enriched White Bread 16 oz (454g), 9pc/box. UPC 0 10314 10004 4. The label is white...

    LL Bakery Inc. of Torrance, CA is recalling all White Farm Enriched White Bread, Butter Farm Enriched White Bread, and Italian Cream Danish because pr...

    LL Bakery, Inc. · Torrance, CA

    Where it was sold: HI, WA, and CA

    UPC 010314100044
    Show details
    Product, as FDA describes it
    Butter Farm Enriched White Bread 16 oz (454g), 9pc/box. UPC 0 10314 10004 4. The label is white with blue and green lettering and red design accents. The LL Bakery Logo is on the bottom left corner.
    Reason, in FDA's words
    LL Bakery Inc. of Torrance, CA is recalling all White Farm Enriched White Bread, Butter Farm Enriched White Bread, and Italian Cream Danish because product labels fail to declare the allergen milk, in the whey powder listed in their ingredient statements.
    Codes on the package
    no lot codes
    Where it was sold
    HI, WA, and CA
    Amount recalled
    1020 units
    Status
    Ended Sep 25, 2013 (FDA lists it as terminated)
    FDA recall number
    F-1475-2013
    View in FDA's recall database
  6. ENDEDClass I · Most seriousRecalled May 18, 2013

    Italian Cream Danish 8.5 oz (240g), 14pc/box. UPC 0 10314 40056 4. The pastry is braided and has...

    LL Bakery Inc. of Torrance, CA is recalling all White Farm Enriched White Bread, Butter Farm Enriched White Bread, and Italian Cream Danish because pr...

    LL Bakery, Inc. · Torrance, CA

    Where it was sold: HI, WA, and CA

    UPC 010314400564
    Show details
    Product, as FDA describes it
    Italian Cream Danish 8.5 oz (240g), 14pc/box. UPC 0 10314 40056 4. The pastry is braided and has yellow creamy swirls and sliced almonds. The label is white with black lettering and a tan colored border. The LL Bakery Logo is on the bottom left corner.
    Reason, in FDA's words
    LL Bakery Inc. of Torrance, CA is recalling all White Farm Enriched White Bread, Butter Farm Enriched White Bread, and Italian Cream Danish because product labels fail to declare the allergen milk, in the whey powder listed in their ingredient statements.
    Codes on the package
    Not available
    Where it was sold
    HI, WA, and CA
    Amount recalled
    1020 units
    Status
    Ended Sep 25, 2013 (FDA lists it as terminated)
    FDA recall number
    F-1476-2013
    View in FDA's recall database
  7. ENDEDClass II · ModerateRecalled May 18, 2013

    Tres Leches cake sold under the following brand names: 1) "****Tres Leches***Postres D'Aqui***D'Aqui...

    Undeclared allergens: soy oil

    D'Aqui Manufacturing Products, Corp., Dba Postres de Aqui · Catano, PR

    Where it was sold: Puerto Rico only.

    Show details
    Product, as FDA describes it
    Tres Leches cake sold under the following brand names: 1) "****Tres Leches***Postres D'Aqui***D'Aqui Manufacturing Products Corp***Peso Neto 3oz***"; 2) "****Tres Leches***Fresh Star***Distribuido por Karelly's Food***PO Box 634 Sabana Seca PR 00952***Peso Neto 3 oz***"
    Reason, in FDA's words
    Undeclared allergens: soy oil
    Codes on the package
    no codes assigned
    Where it was sold
    Puerto Rico only.
    Amount recalled
    1) 10,125 units; 2) 1,410 units
    Status
    Ended Oct 25, 2016 (FDA lists it as terminated)
    FDA recall number
    F-1849-2013
    View in FDA's recall database
  8. ENDEDClass II · ModerateRecalled May 10, 2013

    Gromex Camaron Entero (Whole Shrimp) Net Wt. 1 1/2 oz. 43 First St., Passaic, NJ 07055 (973) 458-93...

    Whole dried shrimp may contain undeclared bi-sulfites. Anelina contains undeclared and unapproved colors..

    Gromex Inc. · Passaic, NJ

    Where it was sold: CT, NJ, NY, PA

    Show details
    Product, as FDA describes it
    Gromex Camaron Entero (Whole Shrimp) Net Wt. 1 1/2 oz. 43 First St., Passaic, NJ 07055 (973) 458-9399
    Reason, in FDA's words
    Whole dried shrimp may contain undeclared bi-sulfites. Anelina contains undeclared and unapproved colors..
    Codes on the package
    None
    Where it was sold
    CT, NJ, NY, PA
    Amount recalled
    unknown
    Status
    Ended Apr 21, 2016 (FDA lists it as terminated)
    FDA recall number
    F-1541-2013
    View in FDA's recall database
  9. ENDEDClass II · ModerateRecalled May 10, 2013

    Gromex Anelina Net Wt. 1/2 oz. Gromex 43 First St., Passaic, NJ 07055 (973) 458-9399

    Whole dried shrimp may contain undeclared bi-sulfites. Anelina contains undeclared and unapproved colors..

    Gromex Inc. · Passaic, NJ

    Where it was sold: CT, NJ, NY, PA

    Show details
    Product, as FDA describes it
    Gromex Anelina Net Wt. 1/2 oz. Gromex 43 First St., Passaic, NJ 07055 (973) 458-9399
    Reason, in FDA's words
    Whole dried shrimp may contain undeclared bi-sulfites. Anelina contains undeclared and unapproved colors..
    Codes on the package
    None
    Where it was sold
    CT, NJ, NY, PA
    Amount recalled
    unknown
    Status
    Ended Apr 21, 2016 (FDA lists it as terminated)
    FDA recall number
    F-1542-2013
    View in FDA's recall database
  10. ENDEDClass I · Most seriousRecalled May 8, 2013

    Whole Foods Salad Chicken Curry , 1 lb plastic bag (bulk)

    Undeclared allergen: egg

    Whole Foods Market Group Inc. · Everett, MA

    Where it was sold: Maine, Massachusetts, Rhode Island, Connecticut, New York, New Jersey

    Show details
    Product, as FDA describes it
    Whole Foods Salad Chicken Curry , 1 lb plastic bag (bulk)
    Reason, in FDA's words
    Undeclared allergen: egg
    Codes on the package
    Sell By Date: 5/10/13
    Where it was sold
    Maine, Massachusetts, Rhode Island, Connecticut, New York, New Jersey
    Amount recalled
    493 lbs
    Status
    Ended Jun 4, 2013 (FDA lists it as terminated)
    FDA recall number
    F-1469-2013
    View in FDA's recall database
  11. ENDEDClass I · Most seriousRecalled May 8, 2013

    Whole Foods Salad Curried Vegan Chick N , 1 lb plastic bags (bulk)

    Undeclared allergen: soy

    Whole Foods Market Group Inc. · Everett, MA

    Where it was sold: Maine, Massachusetts, Rhode Island, Connecticut, New York, New Jersey

    Show details
    Product, as FDA describes it
    Whole Foods Salad Curried Vegan Chick N , 1 lb plastic bags (bulk)
    Reason, in FDA's words
    Undeclared allergen: soy
    Codes on the package
    Sell By Date: 5/10/13
    Where it was sold
    Maine, Massachusetts, Rhode Island, Connecticut, New York, New Jersey
    Amount recalled
    171 lbs
    Status
    Ended Jun 4, 2013 (FDA lists it as terminated)
    FDA recall number
    F-1470-2013
    View in FDA's recall database
  12. ENDEDClass I · Most seriousRecalled May 8, 2013

    IGA Brand Vanilla & Chocolate Ice Cream, 1.75 Quart

    Undeclared allergens: Almonds, Coconut, Soy Lecithin

    Dairy Fresh LLC · Winston Salem, NC

    Where it was sold: FL, GA KY, NC, OH, PA, SC, TN and WV.

    UPC 041370461312
    Show details
    Product, as FDA describes it
    IGA Brand Vanilla & Chocolate Ice Cream, 1.75 Quart
    Reason, in FDA's words
    Undeclared allergens: Almonds, Coconut, Soy Lecithin
    Codes on the package
    UPC #4137046131, Plant Code 3783, Sell by dates: 06-08-13 07-19-13, 08-02-13, 08-13-13 and 08-27-13.
    Where it was sold
    FL, GA KY, NC, OH, PA, SC, TN and WV.
    Amount recalled
    10,050 cartons
    Status
    Ended May 8, 2014 (FDA lists it as terminated)
    FDA recall number
    F-1526-2013
    View in FDA's recall database
  13. ENDEDClass II · ModerateRecalled May 7, 2013

    Market Pantry, Sweet & Salty Mix, NET WT 3 oz (85g), UPC 0 85239 08131 0, INGREDIENTS: Peanuts (pean...

    American Importing Co, Inc is recalling Market Pantry Sweet & Salty Mix because it contains Butter Toffee Peanuts instead of , Honey Roasted Peanuts l...

    American Importing Co, Inc · Minneapolis, MN

    Where it was sold: One main customer, Target Corporation with 52 distribution locations. AL, AZ, CA, CO, GA, IL, IN, IA, KS, MI, MN, NY, NC, OH, OR, PA SC, TX, VA, WI.

    UPC 085239081310
    Show details
    Product, as FDA describes it
    Market Pantry, Sweet & Salty Mix, NET WT 3 oz (85g), UPC 0 85239 08131 0, INGREDIENTS: Peanuts (peanuts...) ...Honey Roasted Peanuts...Honey Roasted Soy Nuts(soybeans...)., CONTAINS PEANUTS AND SOY, May contain tree nuts, milk, wheat and eggs. Distributed by Target Corporation, Minneapolis, MN 55403.
    Reason, in FDA's words
    American Importing Co, Inc is recalling Market Pantry Sweet & Salty Mix because it contains Butter Toffee Peanuts instead of , Honey Roasted Peanuts listed on the label. Butter Toffee Peanuts contain a very small amount of butter (0.5% to 1.0%) which is a milk allergen.
    Codes on the package
    074X348, 092X348, 105X348, 106X348, 107X348, 108X348, 109X348, 112X348, 120X348, 121X348, 122X348.
    Where it was sold
    One main customer, Target Corporation with 52 distribution locations. AL, AZ, CA, CO, GA, IL, IN, IA, KS, MI, MN, NY, NC, OH, OR, PA SC, TX, VA, WI.
    Amount recalled
    2869 cases (24 cups per case)
    Status
    Ended May 26, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1529-2013
    View in FDA's recall database
  14. ENDEDClass I · Most seriousRecalled May 4, 2013

    Pure Herbs, Ltd. Natural Herbal Extracts Protein Dietary Supplement.120mL/4 fl. oz. bottle; 30mL/1 f...

    Pure Herbs, Ltd. Protein Extract contains undeclared milk and soy allergens. People who have an allergy or severe sensitivity to milk or soy run the ...

    Pure Herbs Ltd · Sterling Heights, MI

    Where it was sold: The Pure Herbs products are sold to a network of independent distributors/consumers.

    Show details
    Product, as FDA describes it
    Pure Herbs, Ltd. Natural Herbal Extracts Protein Dietary Supplement.120mL/4 fl. oz. bottle; 30mL/1 fl.oz bottle.
    Reason, in FDA's words
    Pure Herbs, Ltd. Protein Extract contains undeclared milk and soy allergens. People who have an allergy or severe sensitivity to milk or soy run the risk of serious or life-threatening allergic reaction if they consume this product.
    Codes on the package
    Lot codes being recalled are lots 243 and 050812, 012712A.. All Protein products manufactured prior to lot 243 are being recalled. Unfortunately the firm does not have records to indicate the lot numbers prior to lot 243.
    Where it was sold
    The Pure Herbs products are sold to a network of independent distributors/consumers.
    Amount recalled
    813 x 4oz bottles and 72 x 1oz bottles
    Status
    Ended May 12, 2014 (FDA lists it as terminated)
    FDA recall number
    F-1505-2013
    View in FDA's recall database
  15. ENDEDClass I · Most seriousRecalled May 4, 2013

    Hannaford Gourmet Oatmeal Raisin Cookies (9 oz. package) UPC # 0004126872715

    Cookies may contain undeclared tree nuts

    Delhaize America (Hannaford Bros) · South Portland, ME

    Where it was sold: Maine, New Hampshire, Vermont, New York and Massachusetts.

    Show details
    Product, as FDA describes it
    Hannaford Gourmet Oatmeal Raisin Cookies (9 oz. package) UPC # 0004126872715
    Reason, in FDA's words
    Cookies may contain undeclared tree nuts
    Codes on the package
    Sold at retail bakery through 5/6/13
    Where it was sold
    Maine, New Hampshire, Vermont, New York and Massachusetts.
    Amount recalled
    2899- 9 oz cookies
    Status
    Ended Jul 8, 2013 (FDA lists it as terminated)
    FDA recall number
    F-1587-2013
    View in FDA's recall database
  16. ENDEDClass I · Most seriousRecalled May 4, 2013

    Hanna ford Gourmet Cookie Platter (36 oz. package), Includes oatmeal raisin cookies UPC # 04126874...

    Cookies may contain undeclared tree nuts

    Delhaize America (Hannaford Bros) · South Portland, ME

    Where it was sold: Maine, New Hampshire, Vermont, New York and Massachusetts.

    UPC 041268746620
    Show details
    Product, as FDA describes it
    Hanna ford Gourmet Cookie Platter (36 oz. package), Includes oatmeal raisin cookies UPC # 04126874662
    Reason, in FDA's words
    Cookies may contain undeclared tree nuts
    Codes on the package
    Sold at retail bakery through 5/6/13
    Where it was sold
    Maine, New Hampshire, Vermont, New York and Massachusetts.
    Amount recalled
    154 platters (36 oz)
    Status
    Ended Jul 8, 2013 (FDA lists it as terminated)
    FDA recall number
    F-1588-2013
    View in FDA's recall database
  17. ENDEDClass II · ModerateRecalled May 3, 2013

    Senora Verde Taco Dinner Kit, 12ct, 9.75 oz (276g), 12 cartons per case.

    The incorrect taco seasoning pouch, which contained wheat, was placed into the Senora Verde Taco Dinner Kit, which didn't declare wheat, so the produc...

    Gruma Corp · IRVING, TX

    Where it was sold: TX

    Show details
    Product, as FDA describes it
    Senora Verde Taco Dinner Kit, 12ct, 9.75 oz (276g), 12 cartons per case.
    Reason, in FDA's words
    The incorrect taco seasoning pouch, which contained wheat, was placed into the Senora Verde Taco Dinner Kit, which didn't declare wheat, so the product contained undeclared wheat.
    Codes on the package
    DA OCT 29 13 A 09:37
    Where it was sold
    TX
    Amount recalled
    132 cases were shipped and retrieved
    Status
    Ended Jul 29, 2013 (FDA lists it as terminated)
    FDA recall number
    F-1405-2013
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled May 3, 2013

    Talenti Roman Raspberry Sorbetto, 16fl oz, Crafted by Talenti, Marietta, GA 30062

    Undeclared Allergen, Pecans

    Talenti Gelato · Marietta, GA

    Where it was sold: IN

    UPC 186852000822
    Show details
    Product, as FDA describes it
    Talenti Roman Raspberry Sorbetto, 16fl oz, Crafted by Talenti, Marietta, GA 30062
    Reason, in FDA's words
    Undeclared Allergen, Pecans
    Codes on the package
    UPC 1 86852 00082 2, Lot #10/19/2014 M2
    Where it was sold
    IN
    Amount recalled
    420 cases (2260/16 fl oz units)
    Status
    Ended Sep 3, 2013 (FDA lists it as terminated)
    FDA recall number
    F-1464-2013
    View in FDA's recall database
  19. ENDEDClass I · Most seriousRecalled May 1, 2013

    XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Join...

    Undeclared Soy and Milk on the label.

    Atlantic Pro Nutrients, Inc. dba XYMOGEN · Orlando, FL

    Where it was sold: AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NM, NY, OH, OK, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY, District of Columbia ...

    Show details
    Product, as FDA describes it
    XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and 180 capsule bottles
    Reason, in FDA's words
    Undeclared Soy and Milk on the label.
    Codes on the package
    All SKUs
    Where it was sold
    AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NM, NY, OH, OK, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY, District of Columbia and Hawaii
    Amount recalled
    16,268 units
    Status
    Ended Jan 15, 2014 (FDA lists it as terminated)
    FDA recall number
    F-1523-2013
    View in FDA's recall database
  20. ENDEDClass I · Most seriousRecalled Apr 30, 2013

    CARSON'S HOMEMADE PIES AND OTHER GOOD THINGS brand FUDGE BROWNIE COOKIES, NET WT. 14 OZ., UPC 7 5318...

    Carson's Fudge Brownie Cookies contain undeclared walnuts, wheat (flour) and soy (lecithin).

    Carson's Country Market · Lockport, NY

    Where it was sold: New York State

    UPC 753182152400
    Show details
    Product, as FDA describes it
    CARSON'S HOMEMADE PIES AND OTHER GOOD THINGS brand FUDGE BROWNIE COOKIES, NET WT. 14 OZ., UPC 7 53182 15240 0 --- Corner Rt 31 + Rt 93, Lockport, NY 14094 - 716-433-2248 (phone) --- The cookies are packaged in clear, hard plastic containers with seven or eight cookies per container. --- INGREDIENTS: COOKIE: Flour, Sugar, Vegetable Shortening, Evaporated Milk, Eggs, Chocolate Chips, Cocoa, Baking Powder, Vanilla. FROSTING: Sugar, Vegetable Oil, Corn Syrup, Cocoa, Mono + Diglycerides, Polysorbate 60, Potassium Sorbate, Citric Acid, Lecithin, Salt, Flavorings.
    Reason, in FDA's words
    Carson's Fudge Brownie Cookies contain undeclared walnuts, wheat (flour) and soy (lecithin).
    Codes on the package
    "Sell by Dates" of 4/26/2013 to 5/03/13 (date code can be found on the white sticker label found on the top of the hard plastic container)
    Where it was sold
    New York State
    Amount recalled
    UNKNOWN
    Status
    Ended Mar 30, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1382-2013
    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.