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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

28,403 ended recalls · showing 181 to 200

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  1. ENDEDClass II · ModerateRecalled May 5, 2026

    My Wife's Slaw Jalapeno Heat, packaged in 8 oz. and 16 oz. glass mason jars with metal lids/bands, M...

    Product was manufactured and distributed without the benefit of an approved food establishment inspection and the required regulatory safety parameter...

    Jesse Withrow · Zanesville, OH

    Where it was sold: Products distributed directly to end consumers in AL, OH, TX, WV.

    Show details
    Product, as FDA describes it
    My Wife's Slaw Jalapeno Heat, packaged in 8 oz. and 16 oz. glass mason jars with metal lids/bands, MyWifeslaw.web.app, Zanesville, Ohio. Ingredients: Cabbage, Sugar, Vinegar, Mustard, Carrots, Onion, Bell Pepper, Salt, Black Pepper, Cayenne Pepper, Jalapenos, Red Pepper Flakes.
    Reason, in FDA's words
    Product was manufactured and distributed without the benefit of an approved food establishment inspection and the required regulatory safety parameters could not be verified.
    Codes on the package
    No codes applied
    Where it was sold
    Products distributed directly to end consumers in AL, OH, TX, WV.
    Amount recalled
    10 individual units (TOTAL)
    Status
    Ended Jun 26, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0902-2026
    View in FDA's recall database
  2. ENDEDClass II · ModerateRecalled May 4, 2026

    Market of Choice Vegan Kale Caesar Salad, Net Wt. 9.5oz. Finished product is pre-packaged into a cle...

    Undeclared allergen (sesame). Ingredients panel does not list sesame as sub-ingredient of Za'atar spice and Contains statement does not declare sesame...

    Market of Choice Inc · Eugene, OR

    Where it was sold: Only in OR state.

    UPC 210126010993
    Show details
    Product, as FDA describes it
    Market of Choice Vegan Kale Caesar Salad, Net Wt. 9.5oz. Finished product is pre-packaged into a clear flexible plastic clamshell container. Label has UPC 0 210126 01099 3. Market Central Kitchen 1150 Owen Loop S. Eugene, OR 97402 The Za'atar spice, which contains Sesame Seeds, is mixed with chickpeas and packaged into a 2-oz plastic cup. This 2-oz. cup with chickpeas is then assembled into the finished product: a 9.5oz flexible clear plastic clamshell container of Vegan Kale Caesar Salad.
    Reason, in FDA's words
    Undeclared allergen (sesame). Ingredients panel does not list sesame as sub-ingredient of Za'atar spice and Contains statement does not declare sesame.
    Codes on the package
    Expiration dates: 4/20/2026 4/21/2026 4/24/2026 4/25/2026 4/27/2026 4/28/2026 5/1/2026 5/2/2026 5/4/2026 5/5/2026
    Where it was sold
    Only in OR state.
    Amount recalled
    289 (9.5oz) units
    Status
    Ended Jun 8, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0904-2026
    View in FDA's recall database
  3. ENDEDClass I · Most seriousRecalled May 4, 2026

    White Cheddar Seasoning packed in the following sizes and configurations: 1. Net Wt. 1.2 oz (34g)...

    Products were made with recalled California Dairies milk powder due to Salmonella.

    Jonco Industries · Milwaukee, WI

    Where it was sold: MS, WI

    UPC 736659265018
    Show details
    Product, as FDA describes it
    White Cheddar Seasoning packed in the following sizes and configurations: 1. Net Wt. 1.2 oz (34g) Distributed by: Fireworks Popcorn, Division of Jonco Industries, Milwaukee, WI 53218. Sold in a Fireworks Popcorn, Natural American Popcorn Popping & Toppings gift set. Contains: 3 popcorns & 3 popcorns seasonings. 2. Net Wt. 1.6 oz. (45g) UPC 7 36659-26501 8. Distributed by: Fireworks Popcorn, Division of Jonco Industries, Milwaukee, WI 53218. Sold at West Allis Cheese and Sausage retail store. 3. Net Wt 0.7 oz (19g) Williams Sonoma, Not for Retail Sale. Sold in a Williams Sonoma branded Popcorn Sampler Gift Box. Set includes 2 popcorns, oil, seasoning and salt.
    Reason, in FDA's words
    Products were made with recalled California Dairies milk powder due to Salmonella.
    Codes on the package
    1. Lot# 088594-5-1 2. Lot# 088594-7-1 3. Lot# 088594-2-1
    Where it was sold
    MS, WI
    Amount recalled
    1407 jars total
    Status
    Ended Jul 17, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0953-2026
    View in FDA's recall database
  4. ENDEDClass II · ModerateRecalled May 1, 2026

    ...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63oz, 30oz); 126oz UP...

    Undeclared allergen ingredient (fish)

    Ocinet, Inc. · Downey, CA

    Where it was sold: Product was distributed to locations in California, Texas and Georgia.

    UPC 854120040862UPC 085412004112
    Show details
    Product, as FDA describes it
    ...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63oz, 30oz); 126oz UPC- 8541200408 62oz UPC- 8651200409 30oz UPC- 8541200411
    Reason, in FDA's words
    Undeclared allergen ingredient (fish)
    Codes on the package
    No lot numbers provided. Recall includes all product.
    Where it was sold
    Product was distributed to locations in California, Texas and Georgia.
    Amount recalled
    199,750 units (across 3 different sizes)
    Status
    Ended Aug 4, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0780-2026
    View in FDA's recall database
  5. ENDEDClass I · Most seriousRecalled May 1, 2026

    a2 Platinum Premium infant formula Milk-based Powder with Iron 31.7oz (900g) Intended use: infant fo...

    Possible contamination with Cereulide toxin.

    The a2 Milk Company · Boulder, CO

    Where it was sold: The recalled product was distributed throughout the United States.

    UPC 813267020335
    Show details
    Product, as FDA describes it
    a2 Platinum Premium infant formula Milk-based Powder with Iron 31.7oz (900g) Intended use: infant formula (0 12 months). Condition: shelf stable product Type of packaging: metal tin with plastic dust cap. Net weight: 31.7oz (900gm). UPC: 813267020335. Firm name listed on label: The a2 Milk Company. 4909 Pearl East Circle, Suite 300 Boulder CO 80301.
    Reason, in FDA's words
    Possible contamination with Cereulide toxin.
    Codes on the package
    Lot # 2210321712 with Expiration Date: 01/14/2027, Lot # 2210324609 with Expiration Date 01/21/2027, Lot # 2210269454 with Expiration Date 07/15/2026
    Where it was sold
    The recalled product was distributed throughout the United States.
    Amount recalled
    51,202 units
    Status
    Ended Jul 31, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0891-2026
    View in FDA's recall database
  6. ENDEDClass II · ModerateRecalled May 1, 2026

    SECOND NATURE KETO CRUNCH SMART MIX, 10-ounce retail-sized plastic pouch, UPC 077034013405, 6-10oz u...

    The product may contain undeclared allergens (cashews, pistachios), and dried cherries.

    SECOND NATURE BRAND · Madison Heights, MI

    Where it was sold: Distributed nationwide in retail stores and through online orders.

    UPC 077034013405
    Show details
    Product, as FDA describes it
    SECOND NATURE KETO CRUNCH SMART MIX, 10-ounce retail-sized plastic pouch, UPC 077034013405, 6-10oz units per case.
    Reason, in FDA's words
    The product may contain undeclared allergens (cashews, pistachios), and dried cherries.
    Codes on the package
    Best if Used By: 2/12/2027
    Where it was sold
    Distributed nationwide in retail stores and through online orders.
    Amount recalled
    24,756 (10-oz pouch) total units
    Status
    Ended Aug 21, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0905-2026
    View in FDA's recall database
  7. ENDEDClass I · Most seriousRecalled Apr 29, 2026

    6/11oz Sunflower Seeds Salted

    The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

    George J Howe Company, Inc. · Grove City, PA

    Where it was sold: The recalled product was distributed to the following States: AL, AR, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TN, VA,WI,WV,

    Show details
    Product, as FDA describes it
    6/11oz Sunflower Seeds Salted
    Reason, in FDA's words
    The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
    Codes on the package
    07317100316
    Where it was sold
    The recalled product was distributed to the following States: AL, AR, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TN, VA,WI,WV,
    Amount recalled
    1797.67 Cases
    Status
    Ended Sep 10, 2026 (FDA lists it as terminated)
    FDA recall number
    H-1118-2026
    View in FDA's recall database
  8. ENDEDClass I · Most seriousRecalled Apr 29, 2026

    6/11oz No Salt Sunflower Seeds

    The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

    George J Howe Company, Inc. · Grove City, PA

    Where it was sold: The recalled product was distributed to the following States: AL, AR, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TN, VA,WI,WV,

    Show details
    Product, as FDA describes it
    6/11oz No Salt Sunflower Seeds
    Reason, in FDA's words
    The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
    Codes on the package
    07317100320
    Where it was sold
    The recalled product was distributed to the following States: AL, AR, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TN, VA,WI,WV,
    Amount recalled
    578.50 Cases
    Status
    Ended Sep 10, 2026 (FDA lists it as terminated)
    FDA recall number
    H-1119-2026
    View in FDA's recall database
  9. ENDEDClass I · Most seriousRecalled Apr 29, 2026

    8/9.5oz Tub Nut - Sunflower Seed

    The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

    George J Howe Company, Inc. · Grove City, PA

    Where it was sold: The recalled product was distributed to the following States: AL, AR, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TN, VA,WI,WV,

    Show details
    Product, as FDA describes it
    8/9.5oz Tub Nut - Sunflower Seed
    Reason, in FDA's words
    The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
    Codes on the package
    07317102701
    Where it was sold
    The recalled product was distributed to the following States: AL, AR, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TN, VA,WI,WV,
    Amount recalled
    8.00 Cases
    Status
    Ended Sep 10, 2026 (FDA lists it as terminated)
    FDA recall number
    H-1120-2026
    View in FDA's recall database
  10. ENDEDClass I · Most seriousRecalled Apr 29, 2026

    5# Sunflower Seeds C/S

    The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

    George J Howe Company, Inc. · Grove City, PA

    Where it was sold: The recalled product was distributed to the following States: AL, AR, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TN, VA,WI,WV,

    Show details
    Product, as FDA describes it
    5# Sunflower Seeds C/S
    Reason, in FDA's words
    The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
    Codes on the package
    00501138
    Where it was sold
    The recalled product was distributed to the following States: AL, AR, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TN, VA,WI,WV,
    Amount recalled
    19.00 Cases
    Status
    Ended Sep 10, 2026 (FDA lists it as terminated)
    FDA recall number
    H-1121-2026
    View in FDA's recall database
  11. ENDEDClass I · Most seriousRecalled Apr 29, 2026

    5# Sunflower Seeds C/NS

    The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

    George J Howe Company, Inc. · Grove City, PA

    Where it was sold: The recalled product was distributed to the following States: AL, AR, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TN, VA,WI,WV,

    Show details
    Product, as FDA describes it
    5# Sunflower Seeds C/NS
    Reason, in FDA's words
    The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
    Codes on the package
    00501139
    Where it was sold
    The recalled product was distributed to the following States: AL, AR, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TN, VA,WI,WV,
    Amount recalled
    7.00 Cases
    Status
    Ended Sep 10, 2026 (FDA lists it as terminated)
    FDA recall number
    H-1122-2026
    View in FDA's recall database
  12. ENDEDClass I · Most seriousRecalled Apr 29, 2026

    25# Sunflower Seeds C/S

    The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

    George J Howe Company, Inc. · Grove City, PA

    Where it was sold: The recalled product was distributed to the following States: AL, AR, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TN, VA,WI,WV,

    Show details
    Product, as FDA describes it
    25# Sunflower Seeds C/S
    Reason, in FDA's words
    The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
    Codes on the package
    00601138
    Where it was sold
    The recalled product was distributed to the following States: AL, AR, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TN, VA,WI,WV,
    Amount recalled
    2.00 Cases
    Status
    Ended Sep 10, 2026 (FDA lists it as terminated)
    FDA recall number
    H-1123-2026
    View in FDA's recall database
  13. ENDEDClass II · ModerateRecalled Apr 28, 2026

    Prospector Popcorn brand Belgian Chocolate Toffee flavored popcorn; Ingredients: Non-GMO popcorn, br...

    Products contain undeclared soy, specifically soy lecithin.

    Prospector Popcorn, LLC · Ridgefield, CT

    Where it was sold: CT and NY

    UPC 850073852125
    Show details
    Product, as FDA describes it
    Prospector Popcorn brand Belgian Chocolate Toffee flavored popcorn; Ingredients: Non-GMO popcorn, brown sugar, corn syrup, butter, vanilla, baking soda, sea salt, white chocolate (sugar, palm kernel fat, skimmed milk powder [12%], emulsifier [lecithins], natural vanilla flavoring), dark chocolate (sugar, palm kernel fat, fat reduced cocoa powder [20%], emulsifiers [lecithins], natural vanilla flavoring), pretzels (flour, water, salt, malt, dextrose, canola oil, yeast, soda), tofee bits (sugar, butter, almonds), coarse sea salt.; CONTAINS: MILK, TREE NUTS (ALMONDS), WHEAT; Produced in a facility that is shared with gluten, nuts, dairy, and soy.; Manufactured by: Prospector Popcord, LLC, Ridgefield, CT 06877; UPC: 850073852125
    Reason, in FDA's words
    Products contain undeclared soy, specifically soy lecithin.
    Codes on the package
    Expiration dates August 5 - October 24, 2026
    Where it was sold
    CT and NY
    Amount recalled
    140 - 3.5 oz bags
    Status
    Ended (FDA lists it as completed)
    FDA recall number
    H-0779-2026
    View in FDA's recall database
  14. ENDEDClass I · Most seriousRecalled Apr 28, 2026

    MA Cohen's Kippered Herring vacuum packed, weight provided at retail, UPC 7232577992

    Clostridium botulinum is an uncontrolled hazard

    Shining Sea Fish Co. LLC · Detroit, MI

    Where it was sold: MI

    UPC 072325779923
    Show details
    Product, as FDA describes it
    MA Cohen's Kippered Herring vacuum packed, weight provided at retail, UPC 7232577992
    Reason, in FDA's words
    Clostridium botulinum is an uncontrolled hazard
    Codes on the package
    LOT 25079 Expiration May 03 2026, LOT 25055 Expiration May 12 2026, LOT 25028 Expiration June 03 2026, LOT 26344 Expiration July 22 2026
    Where it was sold
    MI
    Amount recalled
    675 pounds
    Status
    Ended Jun 17, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0810-2026
    View in FDA's recall database
  15. ENDEDClass I · Most seriousRecalled Apr 27, 2026

    Kroger HOMESTYLE Cheese AND Garlic CROUTONS NET WT 5 OZ (141g) UPC 0 11110 81353 4 DISTRIBUTED BY TH...

    Possible Salmonella in croutons. The firm was notified by their supplier that the non-fat milk powder used to manufacture the product was recalled due...

    Sugar Foods LLC · Villa Rica, GA

    Where it was sold: Product was shipped to distribution centers in the following states: IN, TN & WI.

    UPC 011110813534
    Show details
    Product, as FDA describes it
    Kroger HOMESTYLE Cheese AND Garlic CROUTONS NET WT 5 OZ (141g) UPC 0 11110 81353 4 DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202
    Reason, in FDA's words
    Possible Salmonella in croutons. The firm was notified by their supplier that the non-fat milk powder used to manufacture the product was recalled due to possible salmonella.
    Codes on the package
    BEST IF USED BY FEB 17 27 BEST IF USED BY FEB 18 27 BEST IF USED BY FEB 27 27 BEST IF USED BY FEB 28 27 BEST IF USED BY MAR 6 27 BEST IF USED BY MAR 9 27 BEST IF USED BY MAR 21 27 BEST IF USED BY APR 1 27 BEST IF USED BY APR 7 27
    Where it was sold
    Product was shipped to distribution centers in the following states: IN, TN & WI.
    Amount recalled
    13,739cs/12/5oz pouches
    Status
    Ended (FDA lists it as completed)
    FDA recall number
    H-0781-2026
    View in FDA's recall database
  16. ENDEDClass II · ModerateRecalled Apr 27, 2026

    Winfield's CWB Chocolate Bar, packed in clear cello bag with fabric bow on top. Manufactured by CBSL...

    Undeclared milk allergen.

    Chocolate Bar Holdings LLC · Houston, TX

    Where it was sold: Houston, TX

    UPC 810079833030UPC 810079833405UPC 810079837892
    Show details
    Product, as FDA describes it
    Winfield's CWB Chocolate Bar, packed in clear cello bag with fabric bow on top. Manufactured by CBSL Commissary (DBA Winfield's Chocolate Bar) 9127 Stella Link Rd Houston Texas. Multiple product shapes/sizes: 1) Cat, Net wt. 8oz (226.8g), UPC: 00810079833030, Unit size 5 x 3 1/2 x 2. 2) Teddy Bear, Net wt. 8oz (226.8g), UPC: 00810079833405, Unit size 5 1/2 x 2 1/2 x 2. 3) Easter Bunny, Net wt. 16oz (453.59g), UPC: 00810079837892, Unit size 4 x 1 x 8 1/2.
    Reason, in FDA's words
    Undeclared milk allergen.
    Codes on the package
    No lot numbers are on these products, so the firm's recall scope is for the entire production line for the following product numbers: 00810079833030 00810079833405 00810079837892
    Where it was sold
    Houston, TX
    Amount recalled
    24 total units (various shapes/sizes)
    Status
    Ended (FDA lists it as completed)
    FDA recall number
    H-1156-2026
    View in FDA's recall database
  17. ENDEDClass II · ModerateRecalled Apr 24, 2026

    Good & Gather Fresh from Our Deli. Sesame Teriyaki Chicken with Rice. Net Wt 18.0 oz (1.125lb). K...

    Undeclared allergens (sesame and soy)

    Target Corporation · Minneapolis, MN

    Where it was sold: AL, AZ, CA, CO, FL, GA, IA, IL, IN, KS, LA, MN, MO, NC, ND, NE, OK, TN, TX, UT, VA, WI

    Show details
    Product, as FDA describes it
    Good & Gather Fresh from Our Deli. Sesame Teriyaki Chicken with Rice. Net Wt 18.0 oz (1.125lb). Keep Refrigerated. DPCI # 878-02-0227. UPC (01) 00250086000009 (3922) 00999. Distributed by SuperTarget Mpls, MN 55403.
    Reason, in FDA's words
    Undeclared allergens (sesame and soy)
    Codes on the package
    Use or Freeze By: 4/15/26 through 4/27/26
    Where it was sold
    AL, AZ, CA, CO, FL, GA, IA, IL, IN, KS, LA, MN, MO, NC, ND, NE, OK, TN, TX, UT, VA, WI
    Amount recalled
    558 units
    Status
    Ended Jul 9, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0761-2026
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled Apr 23, 2026

    Calypso Tropic Tango Lemonade. 16 FL oz (1PT) (473 ML). UPC 0 79581-18709 7. Keep Refrigerated Af...

    Product contains undeclared Yellow No. 5.

    King Juice Company, Inc. · Milwaukee, WI

    Where it was sold: Nationwide. Outside the US to Australia, New Zealand, Singapore, and Trinidad and Tobago

    UPC 079581187097
    Show details
    Product, as FDA describes it
    Calypso Tropic Tango Lemonade. 16 FL oz (1PT) (473 ML). UPC 0 79581-18709 7. Keep Refrigerated After Opening. King Juice Company, Inc., Milwaukee, Wisconsin 53221.
    Reason, in FDA's words
    Product contains undeclared Yellow No. 5.
    Codes on the package
    All Lot Codes including and prior to 01APR2027
    Where it was sold
    Nationwide. Outside the US to Australia, New Zealand, Singapore, and Trinidad and Tobago
    Amount recalled
    299,779 cases (12 bottles per case)
    Status
    Ended Jul 10, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0685-2026
    View in FDA's recall database
  19. ENDEDClass I · Most seriousRecalled Apr 23, 2026

    french broad CHOCOLATE bette's bake sale (a multi-flavor bonbon assortment). 6-piece NET WT. 2.5 OZ ...

    Undeclared nut allergen (walnut) due to mislabeling. The product's printed tasting guide incorrectly identifies the Walnut Fudge and Peach Cobbler fla...

    French Broad Chocolate Factory · Asheville, NC

    Where it was sold: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DC, FL, GA, IA, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, SC, SD, TN,...

    Show details
    Product, as FDA describes it
    french broad CHOCOLATE bette's bake sale (a multi-flavor bonbon assortment). 6-piece NET WT. 2.5 OZ (70.75G); 12-piece NET WT. 5 OZ (141.75G); and 24-piece NET WT. 10 OZ (283.5G), French Broad Chocolate Crafted in Asheville, NC 28801, USA
    Reason, in FDA's words
    Undeclared nut allergen (walnut) due to mislabeling. The product's printed tasting guide incorrectly identifies the Walnut Fudge and Peach Cobbler flavor chocolates (bonbons). Consumers relying on the printed materials could mistakenly consume a nut-containing bonbon.
    Codes on the package
    6-piece: Batch 260414 Best By Jun. 29 2026 & Batch 260417 Best By Jun. 30 2026 12-piece: Batch 260414 Best By Jun. 22 2026 & Batch 260417 Best By Jun. 30 2026 24-piece: Batch 260414 Best By Jun. 29 2026 & Batch 260417 Best By Jun. 30 2026
    Where it was sold
    Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DC, FL, GA, IA, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI & WV.
    Amount recalled
    34/2.5oz boxes, 400/5oz boxes, 53/10oz boxes
    Status
    Ended Sep 1, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0712-2026
    View in FDA's recall database
  20. ENDEDClass II · ModerateRecalled Apr 23, 2026

    Joint Nourish. Dosage:2 tablespoons (30mL). Liquid. For Oral use. Packaging: Plastic Bottle. Net Vol...

    Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen contamination and possible C. Botulinum concerns.

    Wellnov Supplements LLC · Chandler, AZ

    Where it was sold: Products were distributed nationwide and the United States Territory of Puerto Rico.

    Show details
    Product, as FDA describes it
    Joint Nourish. Dosage:2 tablespoons (30mL). Liquid. For Oral use. Packaging: Plastic Bottle. Net Volume:480 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225.
    Reason, in FDA's words
    Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen contamination and possible C. Botulinum concerns.
    Codes on the package
    Distribution dates: 10/01/2025-04/08/2026 Lot Number JN0925 Expiry Date 09/2027
    Where it was sold
    Products were distributed nationwide and the United States Territory of Puerto Rico.
    Amount recalled
    90 bottles
    Status
    Ended Jul 10, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0795-2026
    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.