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

1,060 active recalls · showing 201 to 220

Back to the first page

  1. ACTIVEClass II · ModerateRecalled May 15, 2026

    Ruby, Artichoke Hearts Quartered, 5 LB 8 OZ (2500 G) DRAINED WT 3 LBS 6 OZ (1550G), Can, 6 cans per ...

    Foreign material (Glass) was found in the product.

    GELLERT GLOBAL GROUP · Elizabeth, NJ

    Where it was sold: The adulterated product was sent to the following states. NY,PA,NJ,CT,

    Show details
    Product, as FDA describes it
    Ruby, Artichoke Hearts Quartered, 5 LB 8 OZ (2500 G) DRAINED WT 3 LBS 6 OZ (1550G), Can, 6 cans per case, Store in dry conditions .
    Reason, in FDA's words
    Foreign material (Glass) was found in the product.
    Codes on the package
    P: 25/06/2026 BN: 186/2A E: 24/06/2028 Q.A NG
    Where it was sold
    The adulterated product was sent to the following states. NY,PA,NJ,CT,
    Amount recalled
    1,150 cases
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1176-2026
    View in FDA's recall database
  2. ACTIVEClass I · Most seriousRecalled May 14, 2026

    Enoki Mushroom, Net Weight 150g; Product of Korea; Distributed by IQ Produce UPC: 8809316 814286

    Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Listeria Monocytogenes.

    IQ PRODUCE, LLC · Vernon, CA

    Where it was sold: Product was distributed to 3 California customers.

    UPC 8809316814286
    Show details
    Product, as FDA describes it
    Enoki Mushroom, Net Weight 150g; Product of Korea; Distributed by IQ Produce UPC: 8809316 814286
    Reason, in FDA's words
    Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Listeria Monocytogenes.
    Codes on the package
    Lot UI775
    Where it was sold
    Product was distributed to 3 California customers.
    Amount recalled
    319 units
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0898-2026
    View in FDA's recall database
  3. ACTIVEClass I · Most seriousRecalled May 13, 2026

    Hellas Meze Golden Smoked Whole Herring

    Un-eviscerated fish may be contaminated with clostridium botulinum

    Terra Medi LLC · Long Island City, NY

    Where it was sold: MA, NJ, IL, and NY

    Show details
    Product, as FDA describes it
    Hellas Meze Golden Smoked Whole Herring
    Reason, in FDA's words
    Un-eviscerated fish may be contaminated with clostridium botulinum
    Codes on the package
    production date of 4/12/2025, best before 4/12/2026, L120425F54
    Where it was sold
    MA, NJ, IL, and NY
    Amount recalled
    20 cases (15 units per case)
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0899-2026
    View in FDA's recall database
  4. ACTIVEClass II · ModerateRecalled May 13, 2026

    Nutrisystem, Chocolate Cheesecake, 2 oz (57g) packages, Flow Wrapped, 48 units per case, Keep frozen

    Undeclared Allergen (Soy)

    Nutrisystem Inc · Fort Washington, PA

    Where it was sold: The recalled product was distributed to the following states: AL, AR, CO,GA, IA, IL, IN, KS, KY, LA, MI, MN, MO, MS, ND, NE, NM, OH, OK, SC, SD, TN, TX, WI, WV, WY

    Show details
    Product, as FDA describes it
    Nutrisystem, Chocolate Cheesecake, 2 oz (57g) packages, Flow Wrapped, 48 units per case, Keep frozen
    Reason, in FDA's words
    Undeclared Allergen (Soy)
    Codes on the package
    Product Code: 40007; Lot Code: CH030426
    Where it was sold
    The recalled product was distributed to the following states: AL, AR, CO,GA, IA, IL, IN, KS, KY, LA, MI, MN, MO, MS, ND, NE, NM, OH, OK, SC, SD, TN, TX, WI, WV, WY
    Amount recalled
    5,184 units
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0947-2026
    View in FDA's recall database
  5. ACTIVEClass II · ModerateRecalled May 12, 2026

    STRAUS FAMILY CREAMERY Vanilla Bean ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced and D...

    Potential contamination with foreign objects (metal pieces).

    Straus Family Creamery · Petaluma, CA

    Where it was sold: Domestic: CA, CO, AZ, CT, FL, GA, IA, IL, IN, MD, NJ, OR, PA, SC, TX, WA, WI. Foreign: Not Applicable.

    UPC 784830100306
    Show details
    Product, as FDA describes it
    STRAUS FAMILY CREAMERY Vanilla Bean ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced and Distributed by Straus Family Creamery, Petaluma, CA 94952 UPC: 784830100306
    Reason, in FDA's words
    Potential contamination with foreign objects (metal pieces).
    Codes on the package
    BEST BY: 23 DEC 26; BEST BY: 28 DEC 26
    Where it was sold
    Domestic: CA, CO, AZ, CT, FL, GA, IA, IL, IN, MD, NJ, OR, PA, SC, TX, WA, WI. Foreign: Not Applicable.
    Amount recalled
    3,515 cases (8 units/case)
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0893-2026
    View in FDA's recall database
  6. ACTIVEClass II · ModerateRecalled May 12, 2026

    STRAUS FAMILY CREAMERY Strawberry ORGANIC SUPER PREMIUM ICE CREAM ONE QUART (946mL) ONE PINT (473mL)...

    Potential contamination with foreign objects (metal pieces).

    Straus Family Creamery · Petaluma, CA

    Where it was sold: Domestic: CA, CO, AZ, CT, FL, GA, IA, IL, IN, MD, NJ, OR, PA, SC, TX, WA, WI. Foreign: Not Applicable.

    Show details
    Product, as FDA describes it
    STRAUS FAMILY CREAMERY Strawberry ORGANIC SUPER PREMIUM ICE CREAM ONE QUART (946mL) ONE PINT (473mL) Produced and Distributed by Straus Family Creamery, Petaluma, CA 94952 UPC for QUART: 784830100979 UPC for PINT: 784830100955
    Reason, in FDA's words
    Potential contamination with foreign objects (metal pieces).
    Codes on the package
    QUART - BEST BY: 24 DEC 26; PINT - BEST BY: 25 DEC 26
    Where it was sold
    Domestic: CA, CO, AZ, CT, FL, GA, IA, IL, IN, MD, NJ, OR, PA, SC, TX, WA, WI. Foreign: Not Applicable.
    Amount recalled
    QUART - 273.5 cases (6 units/case); PINT - 754 cases (8 units/case)
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0894-2026
    View in FDA's recall database
  7. ACTIVEClass II · ModerateRecalled May 12, 2026

    STRAUS FAMILY CREAMERY Cookie Dough ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced and D...

    Potential contamination with foreign objects (metal pieces).

    Straus Family Creamery · Petaluma, CA

    Where it was sold: Domestic: CA, CO, AZ, CT, FL, GA, IA, IL, IN, MD, NJ, OR, PA, SC, TX, WA, WI. Foreign: Not Applicable.

    UPC 784830101044
    Show details
    Product, as FDA describes it
    STRAUS FAMILY CREAMERY Cookie Dough ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced and Distributed by Straus Family Creamery, Petaluma, CA 94952 UPC: 784830101044
    Reason, in FDA's words
    Potential contamination with foreign objects (metal pieces).
    Codes on the package
    BEST BY: 26 DEC 26
    Where it was sold
    Domestic: CA, CO, AZ, CT, FL, GA, IA, IL, IN, MD, NJ, OR, PA, SC, TX, WA, WI. Foreign: Not Applicable.
    Amount recalled
    547.375 cases (8 units/case)
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0895-2026
    View in FDA's recall database
  8. ACTIVEClass II · ModerateRecalled May 12, 2026

    STRAUS FAMILY CREAMERY Dutch Chocolate ORGANIC SUPER PREMIUM ICE CREAM ONE QUART (946mL) Produced a...

    Potential contamination with foreign objects (metal pieces).

    Straus Family Creamery · Petaluma, CA

    Where it was sold: Domestic: CA, CO, AZ, CT, FL, GA, IA, IL, IN, MD, NJ, OR, PA, SC, TX, WA, WI. Foreign: Not Applicable.

    UPC 784830100122
    Show details
    Product, as FDA describes it
    STRAUS FAMILY CREAMERY Dutch Chocolate ORGANIC SUPER PREMIUM ICE CREAM ONE QUART (946mL) Produced and Distributed by Straus Family Creamery, Petaluma, CA 94952 UPC: 784830100122
    Reason, in FDA's words
    Potential contamination with foreign objects (metal pieces).
    Codes on the package
    BEST BY: 27 DEC 26
    Where it was sold
    Domestic: CA, CO, AZ, CT, FL, GA, IA, IL, IN, MD, NJ, OR, PA, SC, TX, WA, WI. Foreign: Not Applicable.
    Amount recalled
    637.1665 cases (6 units/case)
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0896-2026
    View in FDA's recall database
  9. ACTIVEClass II · ModerateRecalled May 12, 2026

    STRAUS FAMILY CREAMERY Mint Chip ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced and Dist...

    Potential contamination with foreign objects (metal pieces).

    Straus Family Creamery · Petaluma, CA

    Where it was sold: Domestic: CA, CO, AZ, CT, FL, GA, IA, IL, IN, MD, NJ, OR, PA, SC, TX, WA, WI. Foreign: Not Applicable.

    UPC 784830100504
    Show details
    Product, as FDA describes it
    STRAUS FAMILY CREAMERY Mint Chip ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced and Distributed by Straus Family Creamery, Petaluma, CA 94952 UPC: 784830100504
    Reason, in FDA's words
    Potential contamination with foreign objects (metal pieces).
    Codes on the package
    BEST BY: 30 DEC 26
    Where it was sold
    Domestic: CA, CO, AZ, CT, FL, GA, IA, IL, IN, MD, NJ, OR, PA, SC, TX, WA, WI. Foreign: Not Applicable.
    Amount recalled
    1,127 cases (8 units/case)
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0897-2026
    View in FDA's recall database
  10. ACTIVEClass II · ModerateRecalled May 12, 2026

    Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containing 90 gummies. Net weight: 11.36 ...

    Undeclared melatonin.

    Dkiru LLC · Sheridan, WY

    Where it was sold: Will be provided when available.

    UPC 860008784551
    Show details
    Product, as FDA describes it
    Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containing 90 gummies. Net weight: 11.36 ounces. Serving size: 2 gummies. UPC: 860008784551 Firm name and address listed on label: Dkiru Ltd, Keepers Cottage, 3 Dublin Rd, Leixlip, Co. Kildare W23 H3C4, Ireland
    Reason, in FDA's words
    Undeclared melatonin.
    Codes on the package
    LOT 190824 Expiration Date: 08/19/2026, LOT 240923 Expiration Date: 09/22/2026, and LOT 240929 Expiration Date: 09/28/2026
    Where it was sold
    Will be provided when available.
    Amount recalled
    13,920 bottles
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1079-2026
    View in FDA's recall database
  11. ACTIVEClass I · Most seriousRecalled May 11, 2026

    HH Fresh Trading Corp. (branded) ENOKI MUSHROOM; Premium Quality; Net WT/ Poids Net 150g(5.29oz) Dis...

    Imported Enoki Mushrooms tested positive for Listeria Monocytogenes.

    HH FRESH TRADING CORP · Los Angeles, CA

    Where it was sold: Product was distributed to a single customer located in Texas. Product was further distributed as samples were collected in Florida.

    UPC 4711498860002
    Show details
    Product, as FDA describes it
    HH Fresh Trading Corp. (branded) ENOKI MUSHROOM; Premium Quality; Net WT/ Poids Net 150g(5.29oz) Distributed by HH Fresh Trading Exported by JIA YANG INTERNATIONAL ENTERPRISES CO., LTD. Produced by Green Farm (Taiwan) UPC: 4711498860002
    Reason, in FDA's words
    Imported Enoki Mushrooms tested positive for Listeria Monocytogenes.
    Codes on the package
    No lot codes
    Where it was sold
    Product was distributed to a single customer located in Texas. Product was further distributed as samples were collected in Florida.
    Amount recalled
    120 cases
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0939-2026
    View in FDA's recall database
  12. ACTIVEClass II · ModerateRecalled May 8, 2026

    Lunds & Byerly's Curry Powder Sweet

    Sesame Seeds White were labeled as Curry Powder Sweet.

    J and J Bunting, Inc · Rogers, MN

    Where it was sold: WI

    Show details
    Product, as FDA describes it
    Lunds & Byerly's Curry Powder Sweet
    Reason, in FDA's words
    Sesame Seeds White were labeled as Curry Powder Sweet.
    Codes on the package
    Lot Code 0082026U00232 Best By date: 01/26/2029
    Where it was sold
    WI
    Amount recalled
    144 units (bottles)
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0914-2026
    View in FDA's recall database
  13. ACTIVEClass II · ModerateRecalled May 7, 2026

    Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, Net Wt. 8 FL Oz (237mL) Amber PET mode...

    Foreign object: black particulate matter

    Llorens Pharmaceuticals International Division, Inc. · Miami, FL

    Where it was sold: Distributed to MO, IL, NJ, NY, TX, FL, PR, MA, OK, VA, MN, IA, OH, GA, WI, WA, CA, IN, NC, CO, TN, MA, MO, WV, AZ, DE

    Show details
    Product, as FDA describes it
    Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, Net Wt. 8 FL Oz (237mL) Amber PET modern round 24-400 bottle, 47 SERVING PER BOTTLE, 24 bottles- 8 FL Oz (237mL) Amber PET modern round bottles per package, Store at room. Mnfg by: Llorens Pharmaceutical Miami, FL
    Reason, in FDA's words
    Foreign object: black particulate matter
    Codes on the package
    Lot: B2025 Expiration Date:08/27
    Where it was sold
    Distributed to MO, IL, NJ, NY, TX, FL, PR, MA, OK, VA, MN, IA, OH, GA, WI, WA, CA, IN, NC, CO, TN, MA, MO, WV, AZ, DE
    Amount recalled
    4,196 units
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0809-2026
    View in FDA's recall database
  14. ACTIVEClass II · ModerateRecalled May 6, 2026

    CANNOLI SICILIANI intended use: DESSERT condition: shelf stable shelf life: 12 month type of pack...

    The product contains unapproved colors chlorophyll E140 and E141.

    MID DOLCIARIA SRL · Belpasso

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

    Where it was sold: USA

    UPC 8056093851380
    Show details
    Product, as FDA describes it
    CANNOLI SICILIANI intended use: DESSERT condition: shelf stable shelf life: 12 month type of packaging: box, Net wt. 240g 8.47 oz UPC: 8056093851380 firm name & address listed on label: MID DOLCIARIA SRL VIA CASALINI, 8 -95032 - BELPASSO (CT)
    Reason, in FDA's words
    The product contains unapproved colors chlorophyll E140 and E141.
    Codes on the package
    product code: .110 Sicilian cannoli code, lot/batch code: 2523000008, BEST BEFORE: 10/17/2026
    Where it was sold
    USA
    Amount recalled
    263 boxes total
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0945-2026
    View in FDA's recall database
  15. ACTIVEClass II · ModerateRecalled May 6, 2026

    .155 CRUNCHY CANNOLI GLUTEN FREE intended use: DESSERT condition: shelf stable shelf life: 12 month...

    The product contains unapproved colors chlorophyll E140 and E141.

    MID DOLCIARIA SRL · Belpasso

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

    Where it was sold: USA

    Show details
    Product, as FDA describes it
    .155 CRUNCHY CANNOLI GLUTEN FREE intended use: DESSERT condition: shelf stable shelf life: 12 month type of packaging: box, 190g 6.70 oz - 20 packages per case LOT: 2523000012 - BEST BEFORE: 10/17/2026 firm name & address listed on label: MID DOLCIARIA SRL VIA CASALINI, 8 -95032 - BELPASSO (CT)
    Reason, in FDA's words
    The product contains unapproved colors chlorophyll E140 and E141.
    Codes on the package
    LOT: 2523000012 -10/17/2026
    Where it was sold
    USA
    Amount recalled
    263 boxes total
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0946-2026
    View in FDA's recall database
  16. ACTIVEClass II · ModerateRecalled May 6, 2026

    NEURO NOURISH dietary supplement; 6-IN-1 PREBIOTIC, PROBIOTIC, VITAMIN, MINERAL, FATTY ACID, AND ANT...

    Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste.

    SENSORY SUPPLEMENT LLC · Beverly Hills, CA

    Where it was sold: Product is available nationwide and sold through the firm's online website direct to consumers.

    Show details
    Product, as FDA describes it
    NEURO NOURISH dietary supplement; 6-IN-1 PREBIOTIC, PROBIOTIC, VITAMIN, MINERAL, FATTY ACID, AND ANTIOXIDANT NUTRITIONAL SUPPLEMENT TO SUPPORT DRAIN AND GUT HEALTH NET WT. 5.9 OZ; UPC: 310M5951601
    Reason, in FDA's words
    Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste.
    Codes on the package
    LOT number: 310M5951601 Expiration: 0250A6 EXP 03/2028
    Where it was sold
    Product is available nationwide and sold through the firm's online website direct to consumers.
    Amount recalled
    512 units
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-1109-2026
    View in FDA's recall database
  17. ACTIVEClass I · Most seriousRecalled May 5, 2026

    Southern Style Nuts Gourmet Hunter Mix 23 oz plastic jar UPC 085839073319 and 36 oz plastic jar UPC ...

    potential presence of Salmonella

    JOHN B SANFILIPPO & SONS INC · Elgin, IL

    Where it was sold: Nationwide

    UPC 085839073319UPC 085839071483
    Show details
    Product, as FDA describes it
    Southern Style Nuts Gourmet Hunter Mix 23 oz plastic jar UPC 085839073319 and 36 oz plastic jar UPC 085839071483. 23 oz 6 jars per case case and 96 jars per display. 36 oz 6 jars per case
    Reason, in FDA's words
    potential presence of Salmonella
    Codes on the package
    BEST BY 01/28/27 BEST BY 02/05/27 BEST BY 02/12/27 BEST BY 02/17/27 BEST BY 03/03/27 BEST BY 03/14/27 BEST BY 02/05/27 BEST BY 26/FEB/2027 BEST BY 13/MAR/2027 BEST BY 02/APR/2027
    Where it was sold
    Nationwide
    Amount recalled
    33,176 cases and 22 displays
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0831-2026
    View in FDA's recall database
  18. ACTIVEClass I · Most seriousRecalled May 5, 2026

    Southern Style Nuts Hunter Mix 30 oz plastic jar UPC 085839916302, 4 jars per case

    potential presence of Salmonella

    JOHN B SANFILIPPO & SONS INC · Elgin, IL

    Where it was sold: Nationwide

    UPC 085839916302
    Show details
    Product, as FDA describes it
    Southern Style Nuts Hunter Mix 30 oz plastic jar UPC 085839916302, 4 jars per case
    Reason, in FDA's words
    potential presence of Salmonella
    Codes on the package
    BEST BY 01/29/27 BEST BY 02/03/27 BEST BY 02/10/27 BEST BY 02/19/27 BEST BY 02/24/27 BEST BY 03/02/27 BEST BY 03/10/27 BEST BY 03/16/27
    Where it was sold
    Nationwide
    Amount recalled
    30,515 cases
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0832-2026
    View in FDA's recall database
  19. ACTIVEClass I · Most seriousRecalled May 5, 2026

    Squirrel Brand Travelers Mix 16 oz can UPC 07223899166, 12 cans per case

    potential presence of Salmonella

    JOHN B SANFILIPPO & SONS INC · Elgin, IL

    Where it was sold: Nationwide

    UPC 072238991665
    Show details
    Product, as FDA describes it
    Squirrel Brand Travelers Mix 16 oz can UPC 07223899166, 12 cans per case
    Reason, in FDA's words
    potential presence of Salmonella
    Codes on the package
    BEST BY 04/30/27 BEST BY 05/28/27 BEST BY 06/24/27
    Where it was sold
    Nationwide
    Amount recalled
    3,858 cases
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0833-2026
    View in FDA's recall database
  20. ACTIVEClass I · Most seriousRecalled May 5, 2026

    Squirrel Brand Town & Country Mix 16 oz can UPC 07223805251 and 7.5 oz can UPC 07223805450. 16 oz 1...

    potential presence of Salmonella

    JOHN B SANFILIPPO & SONS INC · Elgin, IL

    Where it was sold: Nationwide

    UPC 072238052519UPC 072238054506
    Show details
    Product, as FDA describes it
    Squirrel Brand Town & Country Mix 16 oz can UPC 07223805251 and 7.5 oz can UPC 07223805450. 16 oz 12 cans per case. 7.5 oz 6 cans per case
    Reason, in FDA's words
    potential presence of Salmonella
    Codes on the package
    BEST BY 05/01/27 BEST BY 05/25/27 BEST BY 05/28/27 BEST BY 02/10/27
    Where it was sold
    Nationwide
    Amount recalled
    3,147 cases
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0834-2026
    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.