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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 ยท Source: U.S. Food and Drug Administration

541 ended recalls ยท showing 301 to 320

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  1. ENDEDClass II ยท 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. ยท 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
  2. ENDEDClass II ยท 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. ยท 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
  3. ENDEDClass I ยท 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. ยท 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
  4. ENDEDClass II ยท 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 ยท 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
  5. ENDEDClass II ยท ModerateRecalled Aug 4, 2017

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

    Product contains undeclared sulfites.

    EL Chilar Huff ยท 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
  6. ENDEDClass II ยท 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 ยท 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
  7. ENDEDClass II ยท 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 ยท 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
  8. ENDEDClass III ยท Low riskRecalled Mar 31, 2017

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

    Presence of Undeclared Sulfites

    GLOBAL COMMODITIES INC ยท 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
  9. ENDEDClass II ยท 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 ยท 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
  10. ENDEDClass II ยท 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 ยท 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
  11. ENDEDClass II ยท 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 ยท 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
  12. ENDEDClass II ยท 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 ยท 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
  13. ENDEDClass II ยท 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 ยท 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
  14. ENDEDClass II ยท 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 ยท 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
  15. ENDEDClass II ยท ModerateRecalled Dec 9, 2016

    The Sweet Dessert Corp., Tres Leches (Three Milk Cake), Peso Neto (Net Weight) 3oz and 4 oz., and 4o...

    Undeclared food color: Yellow #5, Yellow #5 lake, and Yellow #6 and Yellow #6 lake

    Sweets & Desserts, Inc. ยท Aguas Buenas, PR

    Where it was sold: Puerto Rico only

    Show details
    Product, as FDA describes it
    The Sweet Dessert Corp., Tres Leches (Three Milk Cake), Peso Neto (Net Weight) 3oz and 4 oz., and 4oz (large label) Carr. 173 Km 7.1 Bo. Sumidero, Aguas Buenas, P.R. 00703
    Reason, in FDA's words
    Undeclared food color: Yellow #5, Yellow #5 lake, and Yellow #6 and Yellow #6 lake
    Codes on the package
    Unknown
    Where it was sold
    Puerto Rico only
    Amount recalled
    8160 units
    Status
    Ended Oct 15, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1603-2017
  16. ENDEDClass II ยท ModerateRecalled Dec 9, 2016

    The Sweet Dessert Corp., Tres Leches Chocolate (Three Milk Cake with chocolate), Peso Neto (Net Weig...

    Undeclared food color: Yellow #5 and Yellow #5 lake, and Yellow #6 and Yellow #6 lake

    Sweets & Desserts, Inc. ยท Aguas Buenas, PR

    Where it was sold: Puerto Rico only

    Show details
    Product, as FDA describes it
    The Sweet Dessert Corp., Tres Leches Chocolate (Three Milk Cake with chocolate), Peso Neto (Net Weight) 3oz and 4 oz., Carr. 173 Km 7.1 Bo. Sumidero, Aguas Buenas, P.R. 00703
    Reason, in FDA's words
    Undeclared food color: Yellow #5 and Yellow #5 lake, and Yellow #6 and Yellow #6 lake
    Codes on the package
    Unknown
    Where it was sold
    Puerto Rico only
    Amount recalled
    200 units
    Status
    Ended Oct 15, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1604-2017
  17. ENDEDClass II ยท ModerateRecalled Nov 23, 2016

    LONGAN ARIL, NET WT: 10.6oz (300g), contains blue labeling

    The item is subject to Import Alert 21-04 in that it appears to bear or contain cyclamate and dulcin which are unsafe food additives, the item does no...

    Midwest International Corp ยท Brooklyn, NY

    Where it was sold: IL, MA, TX thru 5 retail stores

    Show details
    Product, as FDA describes it
    LONGAN ARIL, NET WT: 10.6oz (300g), contains blue labeling
    Reason, in FDA's words
    The item is subject to Import Alert 21-04 in that it appears to bear or contain cyclamate and dulcin which are unsafe food additives, the item does not declare saccharin on it's labeling and the the product appears to contain or bear the following unsafe color additive such as FD&C Yellow #5 (C.I. No. 19140 - tartrazine) FD&C Red #3 (C.I. No. 45430 - Erythrosine), and Carmoisine (C.I. No. 14720 - former ext. D&C Red #10).
    Codes on the package
    none
    Where it was sold
    IL, MA, TX thru 5 retail stores
    Amount recalled
    39 cartons/30 units
    Status
    Ended Jun 20, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1162-2017
  18. ENDEDClass II ยท ModerateRecalled Nov 23, 2016

    LONGAN ARIL, Net Wt: 7.4oz (210g), contains yellow and orange labeling

    The item is subject to Import Alert 21-04 in that it appears to bear or contain cyclamate and dulcin which are unsafe food additives, the item does no...

    Midwest International Corp ยท Brooklyn, NY

    Where it was sold: IL, MA, TX thru 5 retail stores

    Show details
    Product, as FDA describes it
    LONGAN ARIL, Net Wt: 7.4oz (210g), contains yellow and orange labeling
    Reason, in FDA's words
    The item is subject to Import Alert 21-04 in that it appears to bear or contain cyclamate and dulcin which are unsafe food additives, the item does not declare saccharin on it's labeling and the the product appears to contain or bear the following unsafe color additive such as FD&C Yellow #5 (C.I. No. 19140 - tartrazine) FD&C Red #3 (C.I. No. 45430 - Erythrosine), and Carmoisine (C.I. No. 14720 - former ext. D&C Red #10).
    Codes on the package
    MFD 06/16/2016 EXP 06/15/2018
    Where it was sold
    IL, MA, TX thru 5 retail stores
    Amount recalled
    7 cartons/30 units
    Status
    Ended Jun 20, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1163-2017
  19. ENDEDClass II ยท ModerateRecalled Nov 18, 2016

    Streit's Quinoa with Mushrooms & Herbs, Net Wt. 7.7 oz (220g). Product of Israel

    The Commonwealth of Virginia sampled the product and revealed the presence of undeclared sulfites at 57 ppm and 10 ppm

    ARON STREIT INC ยท Orangeburg, NY

    Where it was sold: IL, MD, CA, & IL

    Show details
    Product, as FDA describes it
    Streit's Quinoa with Mushrooms & Herbs, Net Wt. 7.7 oz (220g). Product of Israel
    Reason, in FDA's words
    The Commonwealth of Virginia sampled the product and revealed the presence of undeclared sulfites at 57 ppm and 10 ppm
    Codes on the package
    Lot numbers: 0045 & 2743
    Where it was sold
    IL, MD, CA, & IL
    Amount recalled
    162 cases
    Status
    Ended Jun 21, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0945-2017
  20. ENDEDClass I ยท Most seriousRecalled Nov 14, 2016

    The Popcorn Shoppe Popcorn Balls (4) 5 oz balls, sold under the brand names of Olde Tyme Recipe, Edw...

    The firm was notified by the state that the labeling for their product failed to declare milk, soy and yellow #5 on their label.

    The Popcorn Shoppe ยท Tiffin, OH

    Where it was sold: Product was shipped to IL & OH.

    Show details
    Product, as FDA describes it
    The Popcorn Shoppe Popcorn Balls (4) 5 oz balls, sold under the brand names of Olde Tyme Recipe, Edwards Orchards & Edwards Orchards West.
    Reason, in FDA's words
    The firm was notified by the state that the labeling for their product failed to declare milk, soy and yellow #5 on their label.
    Codes on the package
    No codees available
    Where it was sold
    Product was shipped to IL & OH.
    Amount recalled
    156cs/30/5 oz bags
    Status
    Ended May 2, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0608-2017

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What the classes mean

Class I ยท Most serious. FDA's highest level: products that could cause serious health problems or death.

Class II ยท Moderate. It may cause temporary health problems, or the risk of serious harm is remote.

Class III ยท 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.