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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

610 recalls · showing 361 to 380

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  1. ENDEDClass II · ModerateRecalled Oct 13, 2017

    033710 - Wegmans Puff Fruit Dumplings, 2 Pack, 6 oz. UPC: 0 77890 33710 3

    Product contains undeclared FD&C Yellow 5 & Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.

    Wegmans Food Markets, Inc. · Rochester, NY

    Where it was sold: NY, MD, VA, PA, MA

    UPC 077890337103
    Show details
    Product, as FDA describes it
    033710 - Wegmans Puff Fruit Dumplings, 2 Pack, 6 oz. UPC: 0 77890 33710 3
    Reason, in FDA's words
    Product contains undeclared FD&C Yellow 5 & Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.
    Codes on the package
    All lot/date codes through 10/15/17
    Where it was sold
    NY, MD, VA, PA, MA
    Amount recalled
    Exact quantity is unknown.
    Status
    Ended Jan 10, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0082-2018
    View in FDA's recall database
  2. ENDEDClass II · ModerateRecalled Oct 13, 2017

    034208 Wegmans Round Danish, 6 pack. UPC: 0 77890 34208 4.

    Product contains undeclared FD&C Yellow 5 & Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.

    Wegmans Food Markets, Inc. · Rochester, NY

    Where it was sold: NY, MD, VA, PA, MA

    UPC 077890342084
    Show details
    Product, as FDA describes it
    034208 Wegmans Round Danish, 6 pack. UPC: 0 77890 34208 4.
    Reason, in FDA's words
    Product contains undeclared FD&C Yellow 5 & Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.
    Codes on the package
    All lot/date codes through 10/15/17
    Where it was sold
    NY, MD, VA, PA, MA
    Amount recalled
    Exact quantity is unknown.
    Status
    Ended Jan 10, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0083-2018
    View in FDA's recall database
  3. ENDEDClass II · ModerateRecalled Oct 13, 2017

    549815- Fruit Fillings Inc. PERFECT NATURAL LEMON TART FILLING Net Weight 24 lb (10.88 kg) 12-2 lb t...

    Product contains undeclared FD&C Yellow 5 & Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.

    Wegmans Food Markets, Inc. · Rochester, NY

    Where it was sold: NY, MD, VA, PA, MA

    Show details
    Product, as FDA describes it
    549815- Fruit Fillings Inc. PERFECT NATURAL LEMON TART FILLING Net Weight 24 lb (10.88 kg) 12-2 lb tubes
    Reason, in FDA's words
    Product contains undeclared FD&C Yellow 5 & Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.
    Codes on the package
    lot codes: 17258073 & 17258074
    Where it was sold
    NY, MD, VA, PA, MA
    Amount recalled
    65 cases
    Status
    Ended Jan 10, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0084-2018
    View in FDA's recall database
  4. ENDEDClass II · ModerateRecalled Oct 13, 2017

    FLAVORx Sweetening Enhancer , the product is packaged as follows: "Sweetening Enhancer AQ, 4oz & ...

    FLAVORx Inc. has decided to recall the following product FLAVORx Sweetening Enhancer, which is a food additive used as a Pharmacy Compounding Material...

    FLAVORx Inc. · Columbia, MD

    Where it was sold: Thru out the United Sates and two foreign countries

    Show details
    Product, as FDA describes it
    FLAVORx Sweetening Enhancer , the product is packaged as follows: "Sweetening Enhancer AQ, 4oz & 1oz Bottles, Lot #161269 / Exp. Date 12/2018 "Sweetening Enhancer AQ, 4oz & 1oz Bottles, Lot #170361 / Exp. Date 03/2019 #100 per box 1oz bottles, #50 per box 4oz bottles Package type: Amber Glass Boston Round Bottles
    Reason, in FDA's words
    FLAVORx Inc. has decided to recall the following product FLAVORx Sweetening Enhancer, which is a food additive used as a Pharmacy Compounding Material, because of subsequent testing of the product in there ongoing stability program indicated that there was microbial growth in their sweetening enhancer product.
    Codes on the package
    "Sweetening Enhancer AQ, 4oz & 1oz Bottles, Lot #161269 / Exp. Date 12/2018 "Sweetening Enhancer AQ, 4oz & 1oz Bottles, Lot #170361 / Exp. Date 03/2019
    Where it was sold
    Thru out the United Sates and two foreign countries
    Amount recalled
    24600 Bottles
    Status
    Ended Jan 2, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0427-2018
    View in FDA's recall database
  5. ENDEDClass II · ModerateRecalled Oct 13, 2017

    FLAVORx Sweetening Enhancer , the product is packaged as follows: Fillmaster Auto Sweetening Enha...

    FLAVORx Inc. has decided to recall the following product FLAVORx Sweetening Enhancer, which is a food additive used as a Pharmacy Compounding Material...

    FLAVORx Inc. · Columbia, MD

    Where it was sold: Thru out the United Sates and two foreign countries

    Show details
    Product, as FDA describes it
    FLAVORx Sweetening Enhancer , the product is packaged as follows: Fillmaster Auto Sweetening Enhancer AQ, 4oz Bottle, Lot #3281712 / Exp. Date 12/2018 Fillmaster Auto Sweetening Enhancer AQ, 4oz Bottle, Lot #4281712 / Exp. Date 03/2019 Fillmaster Auto Sweetening Enhancer AQ, 4oz Bottle, Lot #5181712 / Exp. Date 03/2019 Fillmaster Auto Sweetening Enhancer AQ, 4oz Bottle, Lot #8151712 / Exp. Date 03/2019 Fillmaster Auto Sweetening Enhancer AQ, 4oz Bottle, Lot #8311712 / Exp. Date 03/2019 Fillmaster Auto Sweetening Enhancer AQ, 4oz Bottle, Lot #9011712 / Exp. Date 03/2019 #50 per box 4oz bottles Package type: Amber Glass Boston Round Bottles
    Reason, in FDA's words
    FLAVORx Inc. has decided to recall the following product FLAVORx Sweetening Enhancer, which is a food additive used as a Pharmacy Compounding Material, because of subsequent testing of the product in there ongoing stability program indicated that there was microbial growth in their sweetening enhancer product.
    Codes on the package
    Fillmaster Auto Sweetening Enhancer AQ, 4oz Bottle, Lot #3281712 / Exp. Date 12/2018 Fillmaster Auto Sweetening Enhancer AQ, 4oz Bottle, Lot #4281712 / Exp. Date 03/2019 Fillmaster Auto Sweetening Enhancer AQ, 4oz Bottle, Lot #5181712 / Exp. Date 03/2019 Fillmaster Auto Sweetening Enhancer AQ, 4oz Bottle, Lot #8151712 / Exp. Date 03/2019 Fillmaster Auto Sweetening Enhancer AQ, 4oz Bottle, Lot #8311712 / Exp. Date 03/2019 Fillmaster Auto Sweetening Enhancer AQ, 4oz Bottle, Lot #9011712 / Exp. Date 03/2019
    Where it was sold
    Thru out the United Sates and two foreign countries
    Amount recalled
    420 bottles
    Status
    Ended Jan 2, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0428-2018
    View in FDA's recall database
  6. ENDEDClass II · ModerateRecalled Oct 13, 2017

    FLAVORx Sweetening Enhancer , the product is packaged as follows: Vet Sweetening Enhancer AQ, 2oz...

    FLAVORx Inc. has decided to recall the following product FLAVORx Sweetening Enhancer, which is a food additive used as a Pharmacy Compounding Material...

    FLAVORx Inc. · Columbia, MD

    Where it was sold: Thru out the United Sates and two foreign countries

    Show details
    Product, as FDA describes it
    FLAVORx Sweetening Enhancer , the product is packaged as follows: Vet Sweetening Enhancer AQ, 2oz Bottle, Lot #161269 / Exp. Date 12/2018 Package type: Amber Glass Boston Round Bottles
    Reason, in FDA's words
    FLAVORx Inc. has decided to recall the following product FLAVORx Sweetening Enhancer, which is a food additive used as a Pharmacy Compounding Material, because of subsequent testing of the product in there ongoing stability program indicated that there was microbial growth in their sweetening enhancer product.
    Codes on the package
    Vet Sweetening Enhancer AQ, 2oz Bottle, Lot #161269 / Exp. Date 12/2018
    Where it was sold
    Thru out the United Sates and two foreign countries
    Amount recalled
    2068 bottles
    Status
    Ended Jan 2, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0429-2018
    View in FDA's recall database
  7. ENDEDClass I · Most seriousRecalled Aug 11, 2017

    Gazab Green Raisins, 7 oz. 14 oz. packages, 20/25 packs/carton

    United Trading Inc., has initiated a voluntary recall of Gazab Green Raisins, due to undeclared sulfites.

    United Trading Inc. · Des Plaines, IL

    Where it was sold: Domestic Only: IL, MN, WI, IN, FL, MI, and TX NO VA/DOD

    Show details
    Product, as FDA describes it
    Gazab Green Raisins, 7 oz. 14 oz. packages, 20/25 packs/carton
    Reason, in FDA's words
    United Trading Inc., has initiated a voluntary recall of Gazab Green Raisins, due to undeclared sulfites.
    Codes on the package
    Gazab Green Raisins, Lot#: SBN1612, Sanitary #6500D00045, MFD: 11-22-2016
    Where it was sold
    Domestic Only: IL, MN, WI, IN, FL, MI, and TX NO VA/DOD
    Amount recalled
    14oz - 27 cases (675 pcs were packaged) / 7oz  44.48 cases (1,112 pcs were packaged)
    Status
    Ended Jan 23, 2018 (FDA lists it as terminated)
    FDA recall number
    F-3532-2017
    View in FDA's recall database
  8. ENDEDClass II · ModerateRecalled Aug 10, 2017

    Zydot Ultimate Blend Detox Drink Natural Tropical Ice Flavor 32 fl. oz. (946 ml) and 16 fl. oz. (473...

    Undeclared yellow # 5

    Zydot Unlimited, Inc · Tulsa, OK

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

    Where it was sold: United States

    UPC 054515281409
    Show details
    Product, as FDA describes it
    Zydot Ultimate Blend Detox Drink Natural Tropical Ice Flavor 32 fl. oz. (946 ml) and 16 fl. oz. (473 ml) packaged in clear plastic bottles
    Reason, in FDA's words
    Undeclared yellow # 5
    Codes on the package
    lot 071017LT; UPC 5451528140
    Where it was sold
    United States
    Amount recalled
    9101 bottles
    Status
    Ended Oct 6, 2017 (FDA lists it as terminated)
    FDA recall number
    F-3410-2017
    View in FDA's recall database
  9. ENDEDClass II · ModerateRecalled Aug 4, 2017

    El Chilar Whole Ginger, NET WT 1.25 Oz (35g)

    Product contains undeclared sulfites.

    EL Chilar Huff · Apopka, FL

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

    Where it was sold: U.S. Consignees only.

    Show details
    Product, as FDA describes it
    El Chilar Whole Ginger, NET WT 1.25 Oz (35g)
    Reason, in FDA's words
    Product contains undeclared sulfites.
    Codes on the package
    Lot Number 918 (expiration date: 09/2018)
    Where it was sold
    U.S. Consignees only.
    Amount recalled
    1236 units (103 dozens)
    Status
    Ended Mar 22, 2019 (FDA lists it as terminated)
    FDA recall number
    F-3572-2017
    View in FDA's recall database
  10. ENDEDClass II · ModerateRecalled Jun 8, 2017

    1) Key Lime Dessert Cake, Grandma's Bake Shoppe, NET WT. 14 OZ. (400 g), UPC 8 24153 02582 2

    Product contains certified colors Blue 1 and Yellow 5 which are incorrectly declared as "green color (vegetable and turmeric)."

    Beatrice Bakery Co · Beatrice, NE

    Where it was sold: The recalled product was sold in the firm's retail store in Nebraska and shipped to wholesale accounts in Iowa, Florida, Nebraska, and Vermont.

    UPC 824153025822
    Show details
    Product, as FDA describes it
    1) Key Lime Dessert Cake, Grandma's Bake Shoppe, NET WT. 14 OZ. (400 g), UPC 8 24153 02582 2
    Reason, in FDA's words
    Product contains certified colors Blue 1 and Yellow 5 which are incorrectly declared as "green color (vegetable and turmeric)."
    Codes on the package
    Date codes 17066 and 17110
    Where it was sold
    The recalled product was sold in the firm's retail store in Nebraska and shipped to wholesale accounts in Iowa, Florida, Nebraska, and Vermont.
    Amount recalled
    889 cakes
    Status
    Ended Sep 27, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2874-2017
    View in FDA's recall database
  11. ENDEDClass II · ModerateRecalled May 18, 2017

    Dawn's Foods Tropical Fruit Dip. Nwt WT. 4 lbs. (1.82Kg) Keep Refrigerated. For Foodservice Use o...

    undeclared yellow #5

    Morski Brands, Inc. dba Dawn's Fresh Foods · Portage, WI

    Where it was sold: WI

    Show details
    Product, as FDA describes it
    Dawn's Foods Tropical Fruit Dip. Nwt WT. 4 lbs. (1.82Kg) Keep Refrigerated. For Foodservice Use only.
    Reason, in FDA's words
    undeclared yellow #5
    Codes on the package
    Production #13638
    Where it was sold
    WI
    Amount recalled
    80 lbs. (20 containers)
    Status
    Ended Sep 6, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2397-2017
    View in FDA's recall database
  12. ENDEDClass III · Low riskRecalled Mar 31, 2017

    AAHU BARAH, DRY FIG, NET WT. 1 LB, PRODUCT OF PAKISTAN

    Presence of Undeclared Sulfites

    GLOBAL COMMODITIES INC · Hicksville, NY

    Where it was sold: NY, NJ, MA & VA

    Show details
    Product, as FDA describes it
    AAHU BARAH, DRY FIG, NET WT. 1 LB, PRODUCT OF PAKISTAN
    Reason, in FDA's words
    Presence of Undeclared Sulfites
    Codes on the package
    Best Before: December 2019
    Where it was sold
    NY, NJ, MA & VA
    Amount recalled
    93 cases
    Status
    Ended Jun 17, 2019 (FDA lists it as terminated)
    FDA recall number
    F-2371-2017
    View in FDA's recall database
  13. ENDEDClass II · ModerateRecalled Dec 11, 2016

    Plain Fudge, brand Real Fudge. Product is sold in clear plastic deli container in 8, 12,16, and 24 ...

    Plain 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
    Plain Fudge, brand Real Fudge. Product is sold in clear plastic deli container in 8, 12,16, and 24 oz.
    Reason, in FDA's words
    Plain 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
    290/8 oz. units; 60/12 oz. units; 18/16 oz. units; and 5/24 oz. units
    Status
    Ended Jan 31, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0754-2017
    View in FDA's recall database
  14. ENDEDClass II · ModerateRecalled Dec 11, 2016

    Nutty fudge, brand Real Fudge. Product is sold in clear plastic deli container in 8, 12,16, and 24 o...

    Nutty 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
    Nutty fudge, brand Real Fudge. Product is sold in clear plastic deli container in 8, 12,16, and 24 oz.
    Reason, in FDA's words
    Nutty 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
    261/8 oz. units; 60/12 oz. units; 16/16 oz. units; and 11/24 oz. units
    Status
    Ended Jan 31, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0755-2017
    View in FDA's recall database
  15. ENDEDClass II · ModerateRecalled Dec 11, 2016

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

    Rocky Road 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
    Rocky Road Fudge, brand Real Fudge. Product is sold in clear plastic deli container in 8, 12, and 16 oz.
    Reason, in FDA's words
    Rocky Road 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
    59/8 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-0757-2017
    View in FDA's recall database
  16. ENDEDClass II · ModerateRecalled Dec 11, 2016

    Dark Chocolate Fudge, brand Real Fudge. Product is sold in clear plastic deli container in 8, 16,...

    Dark Chocolate 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
    Dark Chocolate Fudge, brand Real Fudge. Product is sold in clear plastic deli container in 8, 16, and 24 oz.
    Reason, in FDA's words
    Dark Chocolate 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
    82/8 oz. units; 5/16 oz. units; and 2/24 oz.
    Status
    Ended Jan 31, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0758-2017
    View in FDA's recall database
  17. ENDEDClass II · ModerateRecalled Dec 11, 2016

    Salted Caramel Fudge, brand Real Fudge. Product is sold in clear plastic deli container in 8, 16, a...

    Salted Caramel 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
    Salted Caramel Fudge, brand Real Fudge. Product is sold in clear plastic deli container in 8, 16, and 24 oz.
    Reason, in FDA's words
    Salted Caramel 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
    73/8 oz. units; 4/16 oz. units; 3/24 oz. units
    Status
    Ended Jan 31, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0759-2017
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled Dec 11, 2016

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

    White 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
    White Fudge, brand Real Fudge. Product is sold in clear plastic deli container in 8 oz.
    Reason, in FDA's words
    White 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
    16/8 oz units
    Status
    Ended Jan 31, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0760-2017
    View in FDA's recall database
  19. ACTIVEClass II · ModerateRecalled Dec 9, 2016

    Opelle Bakery Egg Bagel (C-105), case of 60 (3.5 oz.), Frozen Raw.

    The Egg Bagel flavor lacks declaration of Yellow 5 on its label.

    O'Pelle Enterprises, Inc. · Pompano Beach, FL

    Where it was sold: Distributed only within Florida.

    Show details
    Product, as FDA describes it
    Opelle Bakery Egg Bagel (C-105), case of 60 (3.5 oz.), Frozen Raw.
    Reason, in FDA's words
    The Egg Bagel flavor lacks declaration of Yellow 5 on its label.
    Codes on the package
    All lot codes of 86 and below
    Where it was sold
    Distributed only within Florida.
    Amount recalled
    9 cases still within shelf-life at initiation of recall
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    F-1330-2017
    View in FDA's recall database
  20. ACTIVEClass II · ModerateRecalled Dec 9, 2016

    Opelle Bakery Egg Bagel (B-105), case of 96 (4 oz.), Frozen Raw.

    The Egg Bagel flavor lacks declaration of Yellow 5 on its label.

    O'Pelle Enterprises, Inc. · Pompano Beach, FL

    Where it was sold: Distributed only within Florida.

    Show details
    Product, as FDA describes it
    Opelle Bakery Egg Bagel (B-105), case of 96 (4 oz.), Frozen Raw.
    Reason, in FDA's words
    The Egg Bagel flavor lacks declaration of Yellow 5 on its label.
    Codes on the package
    All lot codes of 369 and below.
    Where it was sold
    Distributed only within Florida.
    Amount recalled
    101 cases still within shelf-life at initiation of recall
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    F-1331-2017
    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.