Skip to content
NutraDetective

FDA FOOD RECALLS

Look up any food recall

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

Clear all filters
  1. ACTIVEClass III · Low riskRecalled Aug 28, 2026

    Hexing Haw Balls candy, 200g/0.44 lb./7.05 oz bag

    The candy contains the unapproved dye Ponceau 4R.

    Tiffany Food Corp · Brooklyn, NY

    Where it was sold: AZ, NY, CA, FL, GA, IL, MA, MN, NC, NJ, OH, PA, NY, TN, TX, VA

    UPC 6920603810025
    Show details
    Product, as FDA describes it
    Hexing Haw Balls candy; packaged in 200g/0.44 lb./7.05 oz clear plastic bag; Ingredients: haw, white sugar, water.; Serving suggestion: ready to eat. Storage: keep in cool and dry place and keep tightly closed in refrigerator after opening.; PRODUCT OF CHINA; UPC 6 920603 810025
    Reason, in FDA's words
    Unapproved dye Ponceau 4R
    Codes on the package
    Best Before 10/01/2026
    Where it was sold
    AZ, NY, CA, FL, GA, IL, MA, MN, NC, NJ, OH, PA, NY, TN, TX, VA
    Amount recalled
    38 cartons
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1387-2026
    View in FDA's recall database
  2. ACTIVEClass III · Low riskRecalled Jul 28, 2026

    Honeyville YELLOW COLOR 1 GALLON NFI: WATER, FD&C YELLOW #5, FD&C YELLOW #6, CITRIC ACID, AND SODIU...

    Undeclared Red #40.

    FlavorsandColor.Com · Diamond Bar, CA

    Where it was sold: Product is sold to independent manufacturer locations in Nevada, Arizona, Oregon, and California.12 locations total.

    Show details
    Product, as FDA describes it
    Honeyville YELLOW COLOR 1 GALLON NFI: WATER, FD&C YELLOW #5, FD&C YELLOW #6, CITRIC ACID, AND SODIUM BENZOATE. MANUFACTURED FOR: HONEYVILLE, INC. RANCHO CUCAMONGA, CA 91730
    Reason, in FDA's words
    Undeclared Red #40.
    Codes on the package
    Lot: 60609-8 EXP: 06/08/28
    Where it was sold
    Product is sold to independent manufacturer locations in Nevada, Arizona, Oregon, and California.12 locations total.
    Amount recalled
    80 cases
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1225-2026
    View in FDA's recall database
  3. ACTIVEClass III · Low riskRecalled Jul 28, 2026

    Wonton Specialist Inc. Pan Fried Noodle, 16 oz and 5lb

    FD&C Red No. 40 not listed on the label.

    Wonton Specialists · Brooklyn, NY

    Where it was sold: NY, NJ, PA

    Show details
    Product, as FDA describes it
    Wonton Specialist Inc. Pan Fried Noodle, 16 oz and 5lb packaged in clear plastic bags
    Reason, in FDA's words
    Undeclared FD&C Red No. 40
    Codes on the package
    No codes.
    Where it was sold
    NY, NJ, PA
    Amount recalled
    500 bags
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1320-2026
    View in FDA's recall database
  4. ACTIVEClass III · Low riskRecalled Jul 28, 2026

    Wonton Specialist Inc. Wonton Noodle, 12 oz and 5lb

    FD&C Red No. 40 not listed on the label.

    Wonton Specialists · Brooklyn, NY

    Where it was sold: NY, NJ, PA

    Show details
    Product, as FDA describes it
    Wonton Specialist Inc. Wonton Noodle, 12 oz - packaged in foam tray overwrapped with clear plastic and 5lb - packaged in clear plastic bags
    Reason, in FDA's words
    Undeclared FD&C Red No. 40
    Codes on the package
    No codes
    Where it was sold
    NY, NJ, PA
    Amount recalled
    550 bags
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1321-2026
    View in FDA's recall database
  5. ACTIVEClass III · Low riskRecalled Jul 28, 2026

    Wonton Specialist Inc. Lo Mein Noodle, 16 oz

    FD&C Red No. 40 was not listed on the label.

    Wonton Specialists · Brooklyn, NY

    Where it was sold: NY, NJ, PA

    Show details
    Product, as FDA describes it
    Wonton Specialist Inc. Lo Mein Noodle, 16 oz, packaged in clear plastic bags
    Reason, in FDA's words
    Undeclared FD&C Red No. 40
    Codes on the package
    No codes
    Where it was sold
    NY, NJ, PA
    Amount recalled
    300 bags
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1322-2026
    View in FDA's recall database
  6. ACTIVEClass III · Low riskRecalled Jul 28, 2026

    Wonton Specialist Inc. Wonton Skin, 16 oz

    FD&C Red No. 40 not listed on the label.

    Wonton Specialists · Brooklyn, NY

    Where it was sold: NY, NJ, PA

    Show details
    Product, as FDA describes it
    Wonton Specialist Inc. Wonton Skin, 16 oz - packaged in foam tray overwrapped with clear plastic
    Reason, in FDA's words
    Undeclared FD&C Red No. 40
    Codes on the package
    No codes
    Where it was sold
    NY, NJ, PA
    Amount recalled
    480 bags
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1323-2026
    View in FDA's recall database
  7. ACTIVEClass III · Low riskRecalled Jul 28, 2026

    Wonton Specialist Inc. Dumpling Skin, 16 oz

    FD&C Red No. 40 was not listed on the label.

    Wonton Specialists · Brooklyn, NY

    Where it was sold: NY, NJ, PA

    Show details
    Product, as FDA describes it
    Wonton Specialist Inc. Dumpling Skin, 16 oz - packaged in foam tray overwrapped with clear plastic
    Reason, in FDA's words
    Undeclared FD&C Red No. 40
    Codes on the package
    No codes
    Where it was sold
    NY, NJ, PA
    Amount recalled
    240 bags
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1324-2026
    View in FDA's recall database
  8. ACTIVEClass III · Low riskRecalled Jul 28, 2026

    Wonton Specialist Inc. Cooked Noodle, 16 oz and 5 lb

    FD&C Red No. 40 not listed on the label.

    Wonton Specialists · Brooklyn, NY

    Where it was sold: NY, NJ, PA

    Show details
    Product, as FDA describes it
    Wonton Specialist Inc. Cooked Noodle, 16 oz and 5 lb - packaged in clear plastic bags
    Reason, in FDA's words
    Undeclared FD&C Red No. 40
    Codes on the package
    No codes.
    Where it was sold
    NY, NJ, PA
    Amount recalled
    700 bags
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1325-2026
    View in FDA's recall database
  9. ACTIVEClass II · ModerateRecalled Jul 24, 2026

    Elegant Foods Coconut Flakes, 5 Pounds

    Sulfites not listed on the label.

    Elegant Foods, LLC · Madison, WI

    Where it was sold: WI

    Show details
    Product, as FDA describes it
    Elegant Foods Coconut Flakes, 5 Pounds. 537 Atlas Ave, Madison, WI 53714.
    Reason, in FDA's words
    Undeclared sulfites
    Codes on the package
    No code applied.
    Where it was sold
    WI
    Amount recalled
    6 - 5 lb. bags
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1383-2026
    View in FDA's recall database
  10. ACTIVEClass II · ModerateRecalled Jul 24, 2026

    Elegant Foods Golden Raisins, 5 pound

    Sulfites not listed on the label.

    Elegant Foods, LLC · Madison, WI

    Where it was sold: WI

    Show details
    Product, as FDA describes it
    Elegant Foods Golden Raisins, 5 pound. 537 Atlas Ave, Madison, WI 53714.
    Reason, in FDA's words
    Undeclared sulfites
    Codes on the package
    No code applied.
    Where it was sold
    WI
    Amount recalled
    8 - 5 pound bags
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1384-2026
    View in FDA's recall database
  11. ACTIVEClass II · ModerateRecalled Jul 24, 2026

    Elegant Foods Carrot Cake, 9", 14 Servings

    The carrot decoration contains Yellow #5 and Yellow #6, which are not listed on the finished product label.

    Elegant Foods, LLC · Madison, WI

    Where it was sold: WI

    Show details
    Product, as FDA describes it
    Elegant Foods Carrot Cake, 9". 14 Servings. Keep Refrigerated/Frozen. 537 Atlas Ave., Madison, WI 53714.
    Reason, in FDA's words
    Carrot decoration contains Yellow #5 and Yellow #6 which is not listed on finished product label.
    Codes on the package
    No code applied.
    Where it was sold
    WI
    Amount recalled
    300 cakes
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1385-2026
    View in FDA's recall database
  12. ENDEDClass II · ModerateRecalled Jul 8, 2026

    Man Fon Inc. Won Ton Wrappers Extra Thin; Net Wt. 10 oz; UPC# 757168 977315, Keep Refrigerated, Can ...

    Undeclared colors: Yellow#5, and Yellow#6.

    Man Fon, Inc. · San Gabriel, CA

    Where it was sold: Firm distributes primarily to local restaurants (CA) with some of the product intended for retail distribution in grocery stores via a wholesaler (NM).

    UPC 757168977315
    Show details
    Product, as FDA describes it
    Man Fon Inc. Won Ton Wrappers Extra Thin; Net Wt. 10 oz; UPC# 757168 977315, Keep Refrigerated, Can be Frozen. Sold in 48 units (10oz)/case.
    Reason, in FDA's words
    Undeclared colors: Yellow#5, and Yellow#6.
    Codes on the package
    No lot codes.
    Where it was sold
    Firm distributes primarily to local restaurants (CA) with some of the product intended for retail distribution in grocery stores via a wholesaler (NM).
    Amount recalled
    300 lbs
    Status
    Ended Aug 28, 2026 (FDA lists it as terminated)
    FDA recall number
    H-1187-2026
    View in FDA's recall database
  13. ACTIVEClass II · ModerateRecalled Jun 18, 2026

    Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9; Dietary Supplement, 200 Capsules. Serving Size...

    Dietary supplement product Ocular Plus contains undeclared Yellow#5.

    Provision Health Corp. dba PH Labs · San Diego, CA

    Where it was sold: Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.

    Show details
    Product, as FDA describes it
    Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9; Dietary Supplement, 200 Capsules. Serving Size: 4 Capsules; Distributed by: L.A. Farmacia Natural, Burbank, CA 91504 UPC: PHF-C023
    Reason, in FDA's words
    Dietary supplement product Ocular Plus contains undeclared Yellow#5.
    Codes on the package
    Lots: 509011; 506013; 409012; Expiration: 09/27; 06/27; 09/26
    Where it was sold
    Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.
    Amount recalled
    6,967 units across all lots
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1134-2026
    View in FDA's recall database
  14. ACTIVEClass II · ModerateRecalled Jun 18, 2026

    Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Vision of Heal...

    Dietary supplement product Vista MAX contains undeclared Yellow#5.

    Provision Health Corp. dba PH Labs · San Diego, CA

    Where it was sold: Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.

    Show details
    Product, as FDA describes it
    Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Vision of Health, Bell, CA 90201 UPC: PHF-C023
    Reason, in FDA's words
    Dietary supplement product Vista MAX contains undeclared Yellow#5.
    Codes on the package
    Lots: 509011; 506013; 409012; Expiration: 09/27; 06/27; 09/26
    Where it was sold
    Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.
    Amount recalled
    6,967 units across all lots
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1135-2026
    View in FDA's recall database
  15. ENDEDClass II · ModerateRecalled Jun 13, 2026

    Vintage Roots Root Beer Syrup, packaged in glass bottle. Net Wt. 8oz. (236.6 mL). Distributed by Vin...

    Unapproved food additive: sassafras bark.

    Vintage Roots LLC · Conrad, MT

    Where it was sold: Distributed in MT only

    Show details
    Product, as FDA describes it
    Vintage Roots Root Beer Syrup, packaged in glass bottle. Net Wt. 8oz. (236.6 mL). Distributed by Vintage Roots, PO Box 12, Brady, MT 59416. The product label declares: Ingredients: Filtered Water, Pure Cane Sugar, Sassafras Bark, Burdock Roots, Wild Cherry Bark, Molasses, Fresh Lemon Juice, Star Anise, Coriander Seeds, Whole Clove, Wintergreen Extract (no alcohol).
    Reason, in FDA's words
    Unapproved food additive: sassafras bark.
    Codes on the package
    Lot Code: 051626-1 Use By May 2027
    Where it was sold
    Distributed in MT only
    Amount recalled
    7 bottles
    Status
    Ended Jul 28, 2026 (FDA lists it as terminated)
    FDA recall number
    H-1177-2026
    View in FDA's recall database
  16. ENDEDClass III · Low riskRecalled Jun 5, 2026

    The Shadow Loose-Leaf Tea - Winter Spice Black Tea, net wt. 2oz (56 g). Product is packaged in cell...

    Dry tea blends product containing Ashwagandha root which is an unsafe food additive.

    Wild Coast Brew LLC · Coquille, OR

    Where it was sold: Distributed nationwide.

    UPC 198168252543
    Show details
    Product, as FDA describes it
    The Shadow Loose-Leaf Tea - Winter Spice Black Tea, net wt. 2oz (56 g). Product is packaged in cellophane bag within tubular container. UPC 00198168252543. Ingredients: Black Tea ( Keemun & Assam), Cinnamon, Holy Basil, Milky Oats, Licorice Root, Ashwagandha, Ginger. Produced By Wild Coast Brew, Myrtle Point, OR.
    Reason, in FDA's words
    Dry tea blends product containing Ashwagandha root which is an unsafe food additive.
    Codes on the package
    Lot Codes: 09122024 10092025 11252025 02172026
    Where it was sold
    Distributed nationwide.
    Amount recalled
    706 pkg.
    Status
    Ended (FDA lists it as completed)
    FDA recall number
    H-1369-2026
    View in FDA's recall database
  17. ENDEDClass III · Low riskRecalled Jun 5, 2026

    The Creator Loose-Leaf Tea - Ginger Lemongrass Tisane, net wt. 1.5oz (42 g). Product is packaged in...

    Dry tea blends product containing Ashwagandha root which is an unsafe food additive.

    Wild Coast Brew LLC · Coquille, OR

    Where it was sold: Distributed nationwide.

    UPC 198168088265
    Show details
    Product, as FDA describes it
    The Creator Loose-Leaf Tea - Ginger Lemongrass Tisane, net wt. 1.5oz (42 g). Product is packaged in cellophane bag within tubular container. UPC 00198168088265. Ingredients: Oxidized Fireweed, Coriander Seed, Lemongrass, Peppermint, Ginger, Coconut Flakes, Lemon Peel, Ashwagandha, Calendula, Red Pepper Flakes. Produced by Wild Coast Brew, Myrtle Point, OR.
    Reason, in FDA's words
    Dry tea blends product containing Ashwagandha root which is an unsafe food additive.
    Codes on the package
    Lot Codes: 07102025 11052025 11252025 12312025 02262026
    Where it was sold
    Distributed nationwide.
    Amount recalled
    794 pkg.
    Status
    Ended (FDA lists it as completed)
    FDA recall number
    H-1370-2026
    View in FDA's recall database
  18. ENDEDClass III · Low riskRecalled Jun 5, 2026

    The Lover Loose-Leaf Tea - Tart Chocolaty Tisane, net wt. 1.5oz (42 g). Product is packaged in cell...

    Dry tea blends product containing Ashwagandha root which is an unsafe food additive.

    Wild Coast Brew LLC · Coquille, OR

    Where it was sold: Distributed nationwide.

    UPC 198168682364
    Show details
    Product, as FDA describes it
    The Lover Loose-Leaf Tea - Tart Chocolaty Tisane, net wt. 1.5oz (42 g). Product is packaged in cellophane bag within tubular container. UPC 00198168682364. Ingredients: Hibiscus, Cacao Husks, Oxidized Blackberry Leaf, Raspberry Leaf, Rose, Lemon Peel, Peppermint, Ashwagandha, Tangerine oil. Produced By Wild Coast Brew, Myrtle Point, OR.
    Reason, in FDA's words
    Dry tea blends product containing Ashwagandha root which is an unsafe food additive.
    Codes on the package
    Lot Codes: 05222025 06122025 08212025 01222026
    Where it was sold
    Distributed nationwide.
    Amount recalled
    603 pkg.
    Status
    Ended (FDA lists it as completed)
    FDA recall number
    H-1371-2026
    View in FDA's recall database
  19. ACTIVEClass II · ModerateRecalled May 28, 2026

    Wise Onion Rings, 3.75 oz, metalized film in cardboard cartons, 14 bags per case,

    The product contains undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3.

    Wise Foods Inc · Berwick, PA

    Where it was sold: The adulterated product was distributed to the following States: NC, VA, PA, NJ, NY, SC, FL

    UPC 041262288874
    Show details
    Product, as FDA describes it
    Wise Onion Rings, 3.75 oz, metalized film in cardboard cartons, 14 bags per case,
    Reason, in FDA's words
    The product contains undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3.
    Codes on the package
    UPC: 041262288874 Internal production number: 4228887 Lot Codes (expiration date): AUG0326, AUG1026, AUG1726
    Where it was sold
    The adulterated product was distributed to the following States: NC, VA, PA, NJ, NY, SC, FL
    Amount recalled
    490 cases
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1146-2026
    View in FDA's recall database
  20. ACTIVEClass II · ModerateRecalled May 21, 2026

    El David Gelee, Bonbons with fruits Soft & Juicy, 400g. Packaged in decorated paperboard box and cov...

    Undeclared colors (FD&C Yellow 5 and FD&C Red 40).

    Alb-USA Enterprises Inc · Bronx, NY

    Where it was sold: NY, NJ

    UPC 5304000050757
    Show details
    Product, as FDA describes it
    El David Gelee, Bonbons with fruits Soft & Juicy, 400g. Packaged in decorated paperboard box and covered entirely in transparent, flexible plastic wrap. (20 bonbon pieces per 400g box). UPC 5304000050757
    Reason, in FDA's words
    Undeclared colors (FD&C Yellow 5 and FD&C Red 40).
    Codes on the package
    Expiration Date(s): 12.05.2027
    Where it was sold
    NY, NJ
    Amount recalled
    15 (400g) boxed units (20 pieces/box)
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1110-2026
    View in FDA's recall database

Show more recalls

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?

Scan a barcode with the NutraDetective app to check for recalls and see a grade in seconds.

Get the App

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.