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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 341 to 360

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  1. ENDEDClass III · Low riskRecalled Jul 26, 2018

    FP0392, Confidence, Glucosamine Plus, with White Willow Bark & Boswella, 90 Extended Release Tablets...

    Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol 400 and 800 (PEG), Triacetin

    Confidence Inc./Confidence U.S.A. Inc. · Port Washington, NY

    Where it was sold: Nationwide

    UPC 810891022537
    Show details
    Product, as FDA describes it
    FP0392, Confidence, Glucosamine Plus, with White Willow Bark & Boswella, 90 Extended Release Tablets, UPC# 8 10891 02253 7
    Reason, in FDA's words
    Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol 400 and 800 (PEG), Triacetin
    Codes on the package
    Lot# 010216 Lot# 070816 Lot# 090117 Lot# 100817
    Where it was sold
    Nationwide
    Amount recalled
    5,650 bottles in US distribution (total for all products)
    Status
    Ended Oct 22, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1813-2018
    View in FDA's recall database
  2. ENDEDClass III · Low riskRecalled Jul 26, 2018

    FP0292 Confidence Nitro-Cross 60s, UPC# 8 92483 00155 7

    Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol 400 and 800 (PEG), Triacetin

    Confidence Inc./Confidence U.S.A. Inc. · Port Washington, NY

    Where it was sold: Nationwide

    UPC 892483001557
    Show details
    Product, as FDA describes it
    FP0292 Confidence Nitro-Cross 60s, UPC# 8 92483 00155 7
    Reason, in FDA's words
    Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol 400 and 800 (PEG), Triacetin
    Codes on the package
    Lot# 070616
    Where it was sold
    Nationwide
    Amount recalled
    5,650 bottles in US distribution (total for all products)
    Status
    Ended Oct 22, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1814-2018
    View in FDA's recall database
  3. ENDEDClass II · ModerateRecalled Jul 26, 2018

    FP0692, Confidence, Prenatal Multi-V + DHA, 90 tablets per bottle, UPC# 8 10891 02056 4

    Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG), Triacetin, FD&C Yellow #6 ...

    Confidence Inc./Confidence U.S.A. Inc. · Port Washington, NY

    Where it was sold: Nationwide

    UPC 810891020564
    Show details
    Product, as FDA describes it
    FP0692, Confidence, Prenatal Multi-V + DHA, 90 tablets per bottle, UPC# 8 10891 02056 4
    Reason, in FDA's words
    Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG), Triacetin, FD&C Yellow #6 (Sunset Yellow FCF), FD&C Red #40 (Allura Red AC), FD&C Yellow #5 (Tartrazine), and FD&C Blue #2 (Indigotine).
    Codes on the package
    Lot# 110516
    Where it was sold
    Nationwide
    Amount recalled
    5,650 bottles in US distribution (total for all products)
    Status
    Ended Oct 22, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1815-2018
    View in FDA's recall database
  4. ENDEDClass III · Low riskRecalled Jul 26, 2018

    FP0391 Confidence, Glucosamine Plus, With Hyaluronic Acid + Curcumin & Boswellia, 60 Extended Releas...

    Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG), Triacetin.

    Confidence Inc./Confidence U.S.A. Inc. · Port Washington, NY

    Where it was sold: Nationwide

    UPC 892483001069
    Show details
    Product, as FDA describes it
    FP0391 Confidence, Glucosamine Plus, With Hyaluronic Acid + Curcumin & Boswellia, 60 Extended Release Tablets, UPC: 8 92483 00106 9
    Reason, in FDA's words
    Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG), Triacetin.
    Codes on the package
    Lot# 030616
    Where it was sold
    Nationwide
    Amount recalled
    5,650 bottles in US distribution (total for all products)
    Status
    Ended Oct 22, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1816-2018
    View in FDA's recall database
  5. ACTIVEClass III · Low riskRecalled Jul 3, 2018

    PINK LEMONADE COOKIES Byrd's FAMOUS COOKIES; NET WT. 7 OZ .(198g) BOX; BYRD COOKIE COMPANY 6700 WATE...

    Red 40 & Red 3 were not listed in the ingredients statement

    Byrd Cookie Co · Savannah, GA

    Where it was sold: Product was shipped to the following states: AL, CA, GA, OH, OK & PA.

    UPC 748829049465
    Show details
    Product, as FDA describes it
    PINK LEMONADE COOKIES Byrd's FAMOUS COOKIES; NET WT. 7 OZ .(198g) BOX; BYRD COOKIE COMPANY 6700 WATERS SAVANNAH, GA 31406 800-291-2973; UPC 7 48829 04946 5
    Reason, in FDA's words
    Red 40 & Red 3 were not listed in the ingredients statement
    Codes on the package
    Lot Code(s): X356AX, X356BX, Best By Date: 22DEC18 & Lot Code(s): X362AX, X362BX, Best By Date: 28DEC18
    Where it was sold
    Product was shipped to the following states: AL, CA, GA, OH, OK & PA.
    Amount recalled
    20,778 boxes
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    F-1677-2018
    View in FDA's recall database
  6. ENDEDClass II · ModerateRecalled Jun 11, 2018

    FUNKTIONAL FOODS brand SPIRULINA POWDER, NET WEIGHT 3.5 oz (100 g) with UPC Code: 060427570192

    Product contains undeclared sulfites at approx. 40 ppm.

    The TJX Companies, Inc. · Framingham, MA

    Where it was sold: Distributed to TJX retail stored throughout the U.S. with 375 stored listed on the distribution list provided by firm.

    Show details
    Product, as FDA describes it
    FUNKTIONAL FOODS brand SPIRULINA POWDER, NET WEIGHT 3.5 oz (100 g) with UPC Code: 060427570192
    Reason, in FDA's words
    Product contains undeclared sulfites at approx. 40 ppm.
    Codes on the package
    UPC: 060427570192 Lot Code: F-704101
    Where it was sold
    Distributed to TJX retail stored throughout the U.S. with 375 stored listed on the distribution list provided by firm.
    Amount recalled
    1200 units
    Status
    Ended Jul 10, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1609-2018
    View in FDA's recall database
  7. ENDEDClass I · Most seriousRecalled Jun 8, 2018

    Al Reef dried apricot sour, 12 oz., packed in plastic, 24 packages per case

    Golden Star Wholesale, Inc. initiated a voluntary recall of Al Reef dried apricot sour, 12 oz., due to undeclared sulfites.

    Golden Star Wholesale Inc · Troy, MI

    Where it was sold: Domestic: MI, NY,MN,KY,WI,FL,NC,VA,OR,MA,OH,TX,MO Foreign:None

    Show details
    Product, as FDA describes it
    Al Reef dried apricot sour, 12 oz., packed in plastic, 24 packages per case
    Reason, in FDA's words
    Golden Star Wholesale, Inc. initiated a voluntary recall of Al Reef dried apricot sour, 12 oz., due to undeclared sulfites.
    Codes on the package
    Product Code: 061 Dates of distribution: 11/09/2017-05/29/2018
    Where it was sold
    Domestic: MI, NY,MN,KY,WI,FL,NC,VA,OR,MA,OH,TX,MO Foreign:None
    Amount recalled
    816 units
    Status
    Ended Oct 16, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1597-2018
    View in FDA's recall database
  8. ENDEDClass I · Most seriousRecalled May 25, 2018

    WATAN DRY FRUITS PREMIUM QUALITY NATURAL DRIED APRICOT WITH PITT, NET WT. 1 LB, and 0.50 LB, PRODUCE...

    Product contains high levels of undeclared sulfites (2901 ppm).

    Global Commodities Inc · Hicksville, NY

    Where it was sold: VA, NY, VA, NC, MO, FL, GA, ME, NJ

    Show details
    Product, as FDA describes it
    WATAN DRY FRUITS PREMIUM QUALITY NATURAL DRIED APRICOT WITH PITT, NET WT. 1 LB, and 0.50 LB, PRODUCE OF PAKISTAN, IMPORT BY: GLOBAL COMMODITIES INC. NEW YORK USA,
    Reason, in FDA's words
    Product contains high levels of undeclared sulfites (2901 ppm).
    Codes on the package
    Best Before: December 2018
    Where it was sold
    VA, NY, VA, NC, MO, FL, GA, ME, NJ
    Amount recalled
    81 cases (each case contained 30lbs of product)
    Status
    Ended Oct 11, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1565-2018
    View in FDA's recall database
  9. ENDEDClass I · Most seriousRecalled Mar 16, 2018

    EXO Cricket Protein Bar Blueberry Vanilla; Net Wt 2.1 Oz. packaged in a film wrapper, 12 units per c...

    Products contain undeclared sulfites

    Aspire Food Group USA Inc. · Austin, TX

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

    Where it was sold: United States and Germany

    UPC 861703000069
    Show details
    Product, as FDA describes it
    EXO Cricket Protein Bar Blueberry Vanilla; Net Wt 2.1 Oz. packaged in a film wrapper, 12 units per case; UPC: 861703000069
    Reason, in FDA's words
    Products contain undeclared sulfites
    Codes on the package
    26DEC2018 and 06Apr2018
    Where it was sold
    United States and Germany
    Amount recalled
    40,512 units
    Status
    Ended Sep 13, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1111-2018
    View in FDA's recall database
  10. ENDEDClass I · Most seriousRecalled Mar 16, 2018

    EXO Cricket Protein Bar Peanut Butter and Jelly; Net Wt 2.1 Oz. packaged in a film wrapper, 12 units...

    Products contain undeclared sulfites

    Aspire Food Group USA Inc. · Austin, TX

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

    Where it was sold: United States and Germany

    UPC 861703000014
    Show details
    Product, as FDA describes it
    EXO Cricket Protein Bar Peanut Butter and Jelly; Net Wt 2.1 Oz. packaged in a film wrapper, 12 units per case; UPC: 861703000014
    Reason, in FDA's words
    Products contain undeclared sulfites
    Codes on the package
    27DEC2018 and 09Apr2018
    Where it was sold
    United States and Germany
    Amount recalled
    27,128 units
    Status
    Ended Sep 13, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1112-2018
    View in FDA's recall database
  11. ENDEDClass I · Most seriousRecalled Mar 16, 2018

    EXO Cricket Protein Bar Apple Cinnamon; Net Wt. 2.1 Oz. packaged in a film wrapper, 12 units per cas...

    Products contain undeclared sulfites

    Aspire Food Group USA Inc. · Austin, TX

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

    Where it was sold: United States and Germany

    UPC 861703000014
    Show details
    Product, as FDA describes it
    EXO Cricket Protein Bar Apple Cinnamon; Net Wt. 2.1 Oz. packaged in a film wrapper, 12 units per case; UPC: 861703000014
    Reason, in FDA's words
    Products contain undeclared sulfites
    Codes on the package
    08Apr2018
    Where it was sold
    United States and Germany
    Amount recalled
    20,000 units
    Status
    Ended Sep 13, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1113-2018
    View in FDA's recall database
  12. ENDEDClass III · Low riskRecalled Mar 15, 2018

    RALEY'S PISTACHIO GELATO; 10.58 oz. plastic tub UPC: 46567-02382 Ingredients: rehydrated skim...

    Firm was notified by manufacturer in Italy that Pistachio Gelato contained the color sodium copper chlorophyllins (SCC), which is not authorized by FD...

    Raley's Family of Fine Stores · Broderick, CA

    Where it was sold: CA, NV

    UPC 046567023823
    Show details
    Product, as FDA describes it
    RALEY'S PISTACHIO GELATO; 10.58 oz. plastic tub UPC: 46567-02382 Ingredients: rehydrated skimmed milk, sugar, coconut oil, glucose syrup, pure pistachio paste, whole roasted pistachios, milk proteins, mono and diglycerides of fatty acids (emulsifiers), sodium alginate and carob bean gum (thickeners), artificial flavoring, cupric chlorophyllins and turmeric extract (for color). Raley's, West Sacramento, CA
    Reason, in FDA's words
    Firm was notified by manufacturer in Italy that Pistachio Gelato contained the color sodium copper chlorophyllins (SCC), which is not authorized by FDA as a color additive for this product type.
    Codes on the package
    All lots
    Where it was sold
    CA, NV
    Amount recalled
    5,460 units
    Status
    Ended May 22, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1489-2018
    View in FDA's recall database
  13. ENDEDClass I · Most seriousRecalled Mar 6, 2018

    La Marinera, Dried Yellow Potatoes-Papa seca amarilla, NET WEIGHT 10oz (283.5gr.), Imported/Distribu...

    Undeclared Sulfites

    Guixens Food Group, Inc. · Miami, FL

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

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

    Show details
    Product, as FDA describes it
    La Marinera, Dried Yellow Potatoes-Papa seca amarilla, NET WEIGHT 10oz (283.5gr.), Imported/Distributed by: Guixens Food Group, Inc., Expiration date: July 2018
    Reason, in FDA's words
    Undeclared Sulfites
    Codes on the package
    EXPIRATION DATE: JULY 2018
    Where it was sold
    U.S. consignees only.
    Amount recalled
    157 cases/1884 units
    Status
    Ended Feb 12, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1000-2018
    View in FDA's recall database
  14. ENDEDClass I · Most seriousRecalled Mar 6, 2018

    The Peru Chef Dry Potato, Product of Peru, Net Wt. 15oz/425gr, Imported and Distributed by MAS FOOD ...

    A sample was collected by the Florida Department of Agriculture and Consumer Services and the analysis revealed that the product contains undeclared s...

    M.a.s Food Services Co · Lauderdale Lakes, FL

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

    Where it was sold: U.S. consignees and one (1) foreign consignee.

    Show details
    Product, as FDA describes it
    The Peru Chef Dry Potato, Product of Peru, Net Wt. 15oz/425gr, Imported and Distributed by MAS FOOD SERVICES Co.,
    Reason, in FDA's words
    A sample was collected by the Florida Department of Agriculture and Consumer Services and the analysis revealed that the product contains undeclared sulfites.
    Codes on the package
    Exp. Date August 2019
    Where it was sold
    U.S. consignees and one (1) foreign consignee.
    Amount recalled
    50 cases (1200 units)
    Status
    Ended Jun 27, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1115-2018
    View in FDA's recall database
  15. ENDEDClass III · Low riskRecalled Jan 2, 2018

    Wahon Slice Shitake Mushroom 2.5 oz. (71g) UPC : #737483336851

    Undeclared sulfites.

    Vinh Sanh Trading Corp · City of Industry, CA

    Where it was sold: U.S. distribution to the following: CA, IN, VA, PA, FL, CO, GA, KY, AL, TN. No foreign distribution.

    Show details
    Product, as FDA describes it
    Wahon Slice Shitake Mushroom 2.5 oz. (71g) UPC : #737483336851
    Reason, in FDA's words
    Undeclared sulfites.
    Codes on the package
    Expiration Date 2020/03/24
    Where it was sold
    U.S. distribution to the following: CA, IN, VA, PA, FL, CO, GA, KY, AL, TN. No foreign distribution.
    Amount recalled
    141 cartons
    Status
    Ended May 8, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0556-2018
    View in FDA's recall database
  16. ENDEDClass III · Low riskRecalled Nov 17, 2017

    Pure Encapsulations Systemic Enzyme Complex DIETARY SUPPLEMENT 180 CAPSULES UPC: 7 66298 00862 2

    Product contains undeclared sulfites.

    Pure Encapsulations, Inc. · Sudbury, MA

    Where it was sold: NH, AZ, CO, OH, NC

    UPC 766298008622
    Show details
    Product, as FDA describes it
    Pure Encapsulations Systemic Enzyme Complex DIETARY SUPPLEMENT 180 CAPSULES UPC: 7 66298 00862 2
    Reason, in FDA's words
    Product contains undeclared sulfites.
    Codes on the package
    All lots within expiry. Lot/Serial Number: 50074561 50085867 50102085 50107811 50113681 50117860 50121029 50122279 50123772 50129551
    Where it was sold
    NH, AZ, CO, OH, NC
    Amount recalled
    N/A
    Status
    Ended Dec 27, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0396-2018
    View in FDA's recall database
  17. ENDEDClass III · Low riskRecalled Nov 17, 2017

    pure encapsulations AI Enzymes DIETARY SUPPLEMENT 120 CAPSULES UPC: 7 66298 00318 4 and 60 CAPSULES ...

    Product contains undeclared sulfites.

    Pure Encapsulations, Inc. · Sudbury, MA

    Where it was sold: NH, AZ, CO, OH, NC

    UPC 766298003184UPC 766298003177
    Show details
    Product, as FDA describes it
    pure encapsulations AI Enzymes DIETARY SUPPLEMENT 120 CAPSULES UPC: 7 66298 00318 4 and 60 CAPSULES UPC: 7 66298 00317 7
    Reason, in FDA's words
    Product contains undeclared sulfites.
    Codes on the package
    All lots within expiry. AI Enzymes 120: 50048025 50058242 50063516 50067188 50076912 50080121 50092381 50092382 50104459 50108093 50114435 50118464 50125714 AI Enzymes 60: 50048027 50058243 50063517 50067189 50080122 50097606 50104460 50108094 50114436 50118465
    Where it was sold
    NH, AZ, CO, OH, NC
    Amount recalled
    N/A
    Status
    Ended Dec 27, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0397-2018
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled Oct 13, 2017

    038267 - Wegmans Cheese Danish Twist, 13 oz. UPC: 0 77890 38267 7

    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 077890382677
    Show details
    Product, as FDA describes it
    038267 - Wegmans Cheese Danish Twist, 13 oz. UPC: 0 77890 38267 7
    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-0079-2018
    View in FDA's recall database
  19. ENDEDClass II · ModerateRecalled Oct 13, 2017

    038973 - Wegmans Half Cheese Danish Twist, 6 oz. UPC: 0 77890 38973 7

    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 077890389737
    Show details
    Product, as FDA describes it
    038973 - Wegmans Half Cheese Danish Twist, 6 oz. UPC: 0 77890 38973 7
    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-0080-2018
    View in FDA's recall database
  20. ENDEDClass II · ModerateRecalled Oct 13, 2017

    085194 - Wegmans Turnovers, Assorted, 2 Pack, 9 oz. UPC: 0 77890 85194 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 077890851944
    Show details
    Product, as FDA describes it
    085194 - Wegmans Turnovers, Assorted, 2 Pack, 9 oz. UPC: 0 77890 85194 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-0081-2018
    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.