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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 501 to 520

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  1. ENDEDClass I · Most seriousRecalled Nov 21, 2025

    Pinna Grated Pecorino Romano 2/10, 10-pound plastic bags (units)

    Product tested positive for Listeria Monocytogenes.

    Ambriola Co., Inc., The · West Caldwell, NJ

    Where it was sold: The recalled product was distributed to the following states: AZ, CA, CO, CT, DE, FL, GA, IL, IN, MA, ME, NJ, NY, OH, OR, PA, TX, VA, WA, WI

    Show details
    Product, as FDA describes it
    Pinna Grated Pecorino Romano 2/10, 10-pound plastic bags (units)
    Reason, in FDA's words
    Product tested positive for Listeria Monocytogenes.
    Codes on the package
    Lot number(s): 1000572486
    Where it was sold
    The recalled product was distributed to the following states: AZ, CA, CO, CT, DE, FL, GA, IL, IN, MA, ME, NJ, NY, OH, OR, PA, TX, VA, WA, WI
    Amount recalled
    45 Bags (Units)
    Status
    Ended (FDA lists it as completed)
    FDA recall number
    H-0369-2026
    View in FDA's recall database
  2. ENDEDClass I · Most seriousRecalled Nov 21, 2025

    Boar's Head Grated Pecorino Romano, 6 oz Plastic Cup & Lid, 12 units per case

    Product tested positive for Listeria Monocytogenes.

    Ambriola Co., Inc., The · West Caldwell, NJ

    Where it was sold: The recalled product was distributed to the following states: AZ, CA, CO, CT, DE, FL, GA, IL, IN, MA, ME, NJ, NY, OH, OR, PA, TX, VA, WA, WI

    Show details
    Product, as FDA describes it
    Boar's Head Grated Pecorino Romano, 6 oz Plastic Cup & Lid, 12 units per case
    Reason, in FDA's words
    Product tested positive for Listeria Monocytogenes.
    Codes on the package
    Lot number(s): 1000572486
    Where it was sold
    The recalled product was distributed to the following states: AZ, CA, CO, CT, DE, FL, GA, IL, IN, MA, ME, NJ, NY, OH, OR, PA, TX, VA, WA, WI
    Amount recalled
    2,106 Units
    Status
    Ended (FDA lists it as completed)
    FDA recall number
    H-0370-2026
    View in FDA's recall database
  3. ENDEDClass I · Most seriousRecalled Nov 21, 2025

    Sam's Pecorino Romano grated, 1.5 lb Plastic Bags, 12 units per case

    Product tested positive for Listeria Monocytogenes.

    Ambriola Co., Inc., The · West Caldwell, NJ

    Where it was sold: The recalled product was distributed to the following states: AZ, CA, CO, CT, DE, FL, GA, IL, IN, MA, ME, NJ, NY, OH, OR, PA, TX, VA, WA, WI

    Show details
    Product, as FDA describes it
    Sam's Pecorino Romano grated, 1.5 lb Plastic Bags, 12 units per case
    Reason, in FDA's words
    Product tested positive for Listeria Monocytogenes.
    Codes on the package
    Lot number(s): 1000570107 1000570766 1000572513
    Where it was sold
    The recalled product was distributed to the following states: AZ, CA, CO, CT, DE, FL, GA, IL, IN, MA, ME, NJ, NY, OH, OR, PA, TX, VA, WA, WI
    Amount recalled
    1,015 Bags (Units)
    Status
    Ended (FDA lists it as completed)
    FDA recall number
    H-0371-2026
    View in FDA's recall database
  4. ENDEDClass I · Most seriousRecalled Nov 21, 2025

    Boar's Head Pecorino Romano Grated, 5-pound plastic bag (unit)

    Product tested positive for Listeria Monocytogenes.

    Ambriola Co., Inc., The · West Caldwell, NJ

    Where it was sold: The recalled product was distributed to the following states: AZ, CA, CO, CT, DE, FL, GA, IL, IN, MA, ME, NJ, NY, OH, OR, PA, TX, VA, WA, WI

    Show details
    Product, as FDA describes it
    Boar's Head Pecorino Romano Grated, 5-pound plastic bag (unit)
    Reason, in FDA's words
    Product tested positive for Listeria Monocytogenes.
    Codes on the package
    Lot number(s): 1000570093 1000570738
    Where it was sold
    The recalled product was distributed to the following states: AZ, CA, CO, CT, DE, FL, GA, IL, IN, MA, ME, NJ, NY, OH, OR, PA, TX, VA, WA, WI
    Amount recalled
    405 Bags (Units)
    Status
    Ended (FDA lists it as completed)
    FDA recall number
    H-0372-2026
    View in FDA's recall database
  5. ENDEDClass I · Most seriousRecalled Nov 21, 2025

    Ambriola Piccante grated Pecorino Romano, 5 and 10-pound plastic bags (units)

    Product tested positive for Listeria Monocytogenes.

    Ambriola Co., Inc., The · West Caldwell, NJ

    Where it was sold: The recalled product was distributed to the following states: AZ, CA, CO, CT, DE, FL, GA, IL, IN, MA, ME, NJ, NY, OH, OR, PA, TX, VA, WA, WI

    Show details
    Product, as FDA describes it
    Ambriola Piccante grated Pecorino Romano, 5 and 10-pound plastic bags (units)
    Reason, in FDA's words
    Product tested positive for Listeria Monocytogenes.
    Codes on the package
    Lot number(s): 1000572981 1000570737 1000570092 1000572487
    Where it was sold
    The recalled product was distributed to the following states: AZ, CA, CO, CT, DE, FL, GA, IL, IN, MA, ME, NJ, NY, OH, OR, PA, TX, VA, WA, WI
    Amount recalled
    179 Bags (Units)
    Status
    Ended (FDA lists it as completed)
    FDA recall number
    H-0373-2026
    View in FDA's recall database
  6. ENDEDClass I · Most seriousRecalled Nov 21, 2025

    Locatelli Grated Pecorino Romano 48/8oz Shipper, Plastic Cup & Lid, 48 units per case

    Product tested positive for Listeria Monocytogenes.

    Ambriola Co., Inc., The · West Caldwell, NJ

    Where it was sold: The recalled product was distributed to the following states: AZ, CA, CO, CT, DE, FL, GA, IL, IN, MA, ME, NJ, NY, OH, OR, PA, TX, VA, WA, WI

    Show details
    Product, as FDA describes it
    Locatelli Grated Pecorino Romano 48/8oz Shipper, Plastic Cup & Lid, 48 units per case
    Reason, in FDA's words
    Product tested positive for Listeria Monocytogenes.
    Codes on the package
    Lot numbers: 1000570750 1000572499 1000572514
    Where it was sold
    The recalled product was distributed to the following states: AZ, CA, CO, CT, DE, FL, GA, IL, IN, MA, ME, NJ, NY, OH, OR, PA, TX, VA, WA, WI
    Amount recalled
    184 Units
    Status
    Ended (FDA lists it as completed)
    FDA recall number
    H-0374-2026
    View in FDA's recall database
  7. ENDEDClass I · Most seriousRecalled Nov 20, 2025

    Doughy brand Chocolate Chip Cookie Dough; 12 oz

    Product may be contaminated with Salmonella

    HUDSON RIVER FOODS CORP · Castleton, NY

    Where it was sold: TX,NY,PA,FL,NJ,IL,MT,CA,MA,OH,AZ,OR,NC,MD,CO

    Show details
    Product, as FDA describes it
    Doughy brand Chocolate Chip Cookie Dough; 12 oz
    Reason, in FDA's words
    Product may be contaminated with Salmonella
    Codes on the package
    Best By/Expiration Date: July 4, 2026
    Where it was sold
    TX,NY,PA,FL,NJ,IL,MT,CA,MA,OH,AZ,OR,NC,MD,CO
    Amount recalled
    113 units
    Status
    Ended Feb 11, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0239-2026
    View in FDA's recall database
  8. ENDEDClass II · ModerateRecalled Nov 20, 2025

    Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to stop viral replication, expectorant pro...

    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

    A New Life Herbs, LLC · Somerville, TN

    Where it was sold: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN

    UPC 283162814429
    Show details
    Product, as FDA describes it
    Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to stop viral replication, expectorant properties, Contains: Forsethia blossoms, Sumac berries, Pine needles; packaged in a 2 oz. glass dropper bottle, UPC 283162814429
    Reason, in FDA's words
    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
    Codes on the package
    T801AV EXP 9/30 T686AV EXP 12/29 T636AV EXP 9/29 T564AV EXP 9/28
    Where it was sold
    AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
    Amount recalled
    116 bottles
    Status
    Ended Aug 28, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0340-2026
    View in FDA's recall database
  9. ENDEDClass II · ModerateRecalled Nov 20, 2025

    Baby Allergy Herbal Supplement, Contains: Echinacea Purpurea, Oregon Grape Root, Dandelion & Burdock...

    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

    A New Life Herbs, LLC · Somerville, TN

    Where it was sold: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN

    UPC 249953949282
    Show details
    Product, as FDA describes it
    Baby Allergy Herbal Supplement, Contains: Echinacea Purpurea, Oregon Grape Root, Dandelion & Burdock Root, Fenugreek, Ginger Root in vegetable glycerin; packaged in a 2 oz. glass dropper bottle, UPC 249953949282
    Reason, in FDA's words
    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
    Codes on the package
    E166SA EXP 4/28
    Where it was sold
    AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
    Amount recalled
    23 bottles
    Status
    Ended Aug 28, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0341-2026
    View in FDA's recall database
  10. ENDEDClass II · ModerateRecalled Nov 20, 2025

    Baby Soothe Herbal Supplement, Promotes rest, helps ease colic, upset stomach, and teething discomfo...

    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

    A New Life Herbs, LLC · Somerville, TN

    Where it was sold: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN

    Show details
    Product, as FDA describes it
    Baby Soothe Herbal Supplement, Promotes rest, helps ease colic, upset stomach, and teething discomfort, Contains: Catnip, Chamomile, Vegetable Glycerin, water; packaged in a 2 oz. glass dropper bottle
    Reason, in FDA's words
    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
    Codes on the package
    E164BS EXP 1/27 E128BS EXP 7/26
    Where it was sold
    AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
    Amount recalled
    49 bottles
    Status
    Ended Aug 28, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0342-2026
    View in FDA's recall database
  11. ENDEDClass II · ModerateRecalled Nov 20, 2025

    Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Extracted from Frankincense with powerful a...

    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

    A New Life Herbs, LLC · Somerville, TN

    Where it was sold: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN

    UPC 284260392420
    Show details
    Product, as FDA describes it
    Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Extracted from Frankincense with powerful anti-inflammatory properties, useful for pain & inflammation; packaged in a 2 oz. glass dropper bottle, UPC 284260392420
    Reason, in FDA's words
    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
    Codes on the package
    T848B EXP 11/30 T836B EXP 10/30 T808B EXP 9/30 T771B EXP 7/30 T723B EXP 3/30 T696B EXP 1/29 T655B EXP 10/29 T594B EXP 4/29 T536B EXP 10/28
    Where it was sold
    AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
    Amount recalled
    278 bottles
    Status
    Ended Aug 28, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0343-2026
    View in FDA's recall database
  12. ENDEDClass II · ModerateRecalled Nov 20, 2025

    Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract, Supports a healthy immune system with ...

    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

    A New Life Herbs, LLC · Somerville, TN

    Where it was sold: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN

    UPC 284588087831
    Show details
    Product, as FDA describes it
    Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract, Supports a healthy immune system with anti-cancer properties; packaged in a 2 oz. glass dropper bottle, UPC 284588087831
    Reason, in FDA's words
    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
    Codes on the package
    T720CH EXP 3/30 T656CH EXP 10/29 T618CH EXP 7/29 T568CH EXP 1/29 T532CH EXP 10/28
    Where it was sold
    AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
    Amount recalled
    144 bottles
    Status
    Ended Aug 28, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0344-2026
    View in FDA's recall database
  13. ENDEDClass II · ModerateRecalled Nov 20, 2025

    Ear Drops Herbal Supplement, Mullein flower alcohol tincture 1:5, Pain relieving and antibiotic prop...

    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

    A New Life Herbs, LLC · Somerville, TN

    Where it was sold: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN

    Show details
    Product, as FDA describes it
    Ear Drops Herbal Supplement, Mullein flower alcohol tincture 1:5, Pain relieving and antibiotic properties, packaged in a 0.5 oz. plastic dropper bottle
    Reason, in FDA's words
    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
    Codes on the package
    T553MF EXP 12/28
    Where it was sold
    AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
    Amount recalled
    22 bottles
    Status
    Ended Aug 28, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0345-2026
    View in FDA's recall database
  14. ENDEDClass II · ModerateRecalled Nov 20, 2025

    Organic Ginger Root Herbal Supplement, Natural anti-inflammatory properties, supports gut, increases...

    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

    A New Life Herbs, LLC · Somerville, TN

    Where it was sold: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN

    Show details
    Product, as FDA describes it
    Organic Ginger Root Herbal Supplement, Natural anti-inflammatory properties, supports gut, increases circulation, 50 capsules/560 mg, packaged in a plastic bag
    Reason, in FDA's words
    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
    Codes on the package
    C132GR EXP 7/27 C131GR EXP 6/27 C121GR EXP 2/27 C115GR EXP 12/26 C108GR EXP 1/26 C93GR EXP 7/25
    Where it was sold
    AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
    Amount recalled
    48 bags
    Status
    Ended Aug 28, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0346-2026
    View in FDA's recall database
  15. ENDEDClass II · ModerateRecalled Nov 20, 2025

    Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, Wood Betony & White Willow in...

    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

    A New Life Herbs, LLC · Somerville, TN

    Where it was sold: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN

    UPC 231946534537
    Show details
    Product, as FDA describes it
    Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, Wood Betony & White Willow in vegetable glycerin, packaged in a 4.5 oz. glass bottle or 9 oz. glass bottle, UPC 231946534537
    Reason, in FDA's words
    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
    Codes on the package
    E170PA EXP 7/28 E174PA EXP 9/28 E161PA EXP 12/27 E146PA EXP 12/26 E123PA EXP 7/26 E110PA EXP 10/25 E93PA EXP 2/25
    Where it was sold
    AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
    Amount recalled
    275 bottles
    Status
    Ended Aug 28, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0347-2026
    View in FDA's recall database
  16. ENDEDClass II · ModerateRecalled Nov 20, 2025

    Sinus Cap Herbal Supplement, Herbs containing antibiotic, drying, expectorant, and emollient propert...

    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

    A New Life Herbs, LLC · Somerville, TN

    Where it was sold: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN

    Show details
    Product, as FDA describes it
    Sinus Cap Herbal Supplement, Herbs containing antibiotic, drying, expectorant, and emollient properties, Fenugreek, Thyme, Oregon Grape Root, & Bentonite Clay, 50 capsules/510 mg; packaged in a plastic bag
    Reason, in FDA's words
    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
    Codes on the package
    C136SC EXP 10/27 C128SC EXP 5/27 C110SC EXP 9/26 C109SC EXP 4/26 C102SC EXP 10/25
    Where it was sold
    AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
    Amount recalled
    38 bags
    Status
    Ended Aug 28, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0348-2026
    View in FDA's recall database
  17. ENDEDClass I · Most seriousRecalled Nov 19, 2025

    Sonex brand aluminum pot; ISO 9001:2000; Made in Pakistan

    Products found to contain leachable lead levels (0.323mg/L)

    Alanwar Food Corp. · Brooklyn, NY

    Where it was sold: NY

    Show details
    Product, as FDA describes it
    Sonex brand aluminum pot; ISO 9001:2000; Made in Pakistan
    Reason, in FDA's words
    Products found to contain leachable lead levels (0.323mg/L)
    Codes on the package
    No codes
    Where it was sold
    NY
    Amount recalled
    2 units
    Status
    Ended Mar 6, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0234-2026
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled Nov 19, 2025

    Chef brand Milk Pan 24cm

    Products found to contain leachable lead levels (3.00 mg/L)

    Shata Traders Inc. · Brooklyn, NY

    Where it was sold: NY, NJ, CT, MA, MD, VA PA

    Show details
    Product, as FDA describes it
    Chef brand Milk Pan 24cm
    Reason, in FDA's words
    Products found to contain leachable lead levels (3.00 mg/L)
    Codes on the package
    No codes
    Where it was sold
    NY, NJ, CT, MA, MD, VA PA
    Amount recalled
    145 boxes
    Status
    Ended Mar 9, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0306-2026
    View in FDA's recall database
  19. ENDEDClass II · ModerateRecalled Nov 19, 2025

    Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case

    Product tested high for lead.

    GUSTO GROUP, INC. · Paterson, NJ

    Where it was sold: The recalled product was distributed to the following states: IA, NJ

    Show details
    Product, as FDA describes it
    Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case
    Reason, in FDA's words
    Product tested high for lead.
    Codes on the package
    DPA159 Shrimp Paste (Klong Kone) 'M'
    Where it was sold
    The recalled product was distributed to the following states: IA, NJ
    Amount recalled
    7 cases
    Status
    Ended Apr 7, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0389-2026
    View in FDA's recall database
  20. ENDEDClass II · ModerateRecalled Nov 19, 2025

    DPA161 Shrimp Paste (Klong Kone) 'L' , 32 oz, 12 count , PLastic Jar, 12 packages / cases

    Product tested high for lead.

    GUSTO GROUP, INC. · Paterson, NJ

    Where it was sold: The recalled product was distributed to the following states: IA, NJ

    Show details
    Product, as FDA describes it
    DPA161 Shrimp Paste (Klong Kone) 'L' , 32 oz, 12 count , PLastic Jar, 12 packages / cases
    Reason, in FDA's words
    Product tested high for lead.
    Codes on the package
    DPA161 Shrimp Paste (Klong Kone) 'L'
    Where it was sold
    The recalled product was distributed to the following states: IA, NJ
    Amount recalled
    7 cases
    Status
    Ended Apr 7, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0390-2026
    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.