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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 341 to 360

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  1. ACTIVEClass II · ModerateRecalled Apr 15, 2026

    Chocolate Showers Ice Cream - 32 oz (5 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine...

    Undeclared Soy (with mitigating circumstances)

    Silver Moon LP dba Loard's Ice Cream · San Leandro, CA

    Where it was sold: Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.

    UPC 812017009187
    Show details
    Product, as FDA describes it
    Chocolate Showers Ice Cream - 32 oz (5 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods, and Berkeley Bowl) UPC: 8-12017-00918
    Reason, in FDA's words
    Undeclared Soy (with mitigating circumstances)
    Codes on the package
    UPC: 8-12017-00918
    Where it was sold
    Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.
    Amount recalled
    1396 TOTAL units (32 oz/unit)
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0760-2026
    View in FDA's recall database
  2. ACTIVEClass II · ModerateRecalled Apr 13, 2026

    52USA brand POPPING BOBA; STRAWBERRY FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fruct...

    Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).

    Guangdong Zonegoing Food Co., LTD · Huizhou

    Where it was sold: NY

    UPC 810185421237
    Show details
    Product, as FDA describes it
    52USA brand POPPING BOBA; STRAWBERRY FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food additives (hydroxypropyl distarch phosphate (E1442), calcium lactate (E327), DL-malic acid (E296), sodium alginate (E401), citric acid (E330), carageenan (EE407), potassium chloride (E508), potassium sorbate (E202), guar gum (E412), trisodium citrate (E331), sucralose (E955), allura red (E129), food flavors.; CONTAINS NO JUICE; Shelf Life: 18 months; Distributed for Felicific Inc., Queens, NY 11435; PRODUCT OF CHINA; UPC 8 10185 42123 7
    Reason, in FDA's words
    Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).
    Codes on the package
    Lot Numbers: 20250813 Expiration Date: Feb 8, 2027
    Where it was sold
    NY
    Amount recalled
    5,196 units (total)
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0676-2026
    View in FDA's recall database
  3. ACTIVEClass II · ModerateRecalled Apr 13, 2026

    52USA brand POPPING BOBA; PASSION FRUIT FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fr...

    Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).

    Guangdong Zonegoing Food Co., LTD · Huizhou

    Where it was sold: NY

    UPC 810184212515
    Show details
    Product, as FDA describes it
    52USA brand POPPING BOBA; PASSION FRUIT FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food additives (hydroxypropyl distarch phosphate (E1442), calcium lactate (E327), DL-malic acid (E296), sodium alginate (E401), citric acid (E330), carrageenan (EE407), potassium chloride (E508), potassium sorbate (E202), guar gum (E412), trisodium citrate (E331), beta-carotene (E160a). sucralose (E955), tartrazine (E102), sunset yellow (E110)), food flavors.; CONTAINS NO JUICE; Shelf Life: 18 months; Distributed for Felicific Inc., Queens, NY 11435; PRODUCT OF CHINA; UPC 8 1018 42125 1
    Reason, in FDA's words
    Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).
    Codes on the package
    Lot Numbers: 20250813 Expiration Date: Feb 8, 2027
    Where it was sold
    NY
    Amount recalled
    5,196 units (total)
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0677-2026
    View in FDA's recall database
  4. ACTIVEClass II · ModerateRecalled Apr 13, 2026

    52USA brand POPPING BOBA; MANGO FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose s...

    Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).

    Guangdong Zonegoing Food Co., LTD · Huizhou

    Where it was sold: NY

    UPC 810184212447
    Show details
    Product, as FDA describes it
    52USA brand POPPING BOBA; MANGO FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food additives (hydroxypropyl distarch phosphate (E1442), calcium lactate (E327), DL-malic acid (E296), sodium alginate (E401), citric acid (E330), carrageenan (EE407), potassium chloride (E508), potassium sorbate (E202), guar gum (E412), trisodium citrate (E331), beta-carotene (E160a). sucralose (E955), tartrazine (E102), sunset yellow (E110)), food flavors.; CONTAINS NO JUICE; Shelf Life: 18 months; Distributed for Felicific Inc., Queens, NY 11435; PRODUCT OF CHINA; UPC 8 1018 42124 4
    Reason, in FDA's words
    Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).
    Codes on the package
    Lot Numbers: 20250813 Expiration Date: Feb 8, 2027
    Where it was sold
    NY
    Amount recalled
    5,196 units (total)
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0678-2026
    View in FDA's recall database
  5. ACTIVEClass II · ModerateRecalled Apr 7, 2026

    Bulk Horchata Powder 3951 (100547) 1/25 HORCHATA UPC: 042743-19015-0 Item: 100547

    Undeclared milk.

    Marquez Brothers International, Inc. · Fresno, CA

    Where it was sold: Domestic distribution: AK, AL, AR, AZ, CA, CO, FL, IA, ID, IL, IN, KS, LA, MI, MN, MO, MT, NE, NM, NV, OH, OK, OR, TN, TX, UT, VA, WA, WI. Foreign distribution: Canada, Japan.

    UPC 042743190150
    Show details
    Product, as FDA describes it
    Bulk Horchata Powder 3951 (100547) 1/25 HORCHATA UPC: 042743-19015-0 Item: 100547
    Reason, in FDA's words
    Undeclared milk.
    Codes on the package
    Lot, Expiration: HR02224, 01/23/26; HR06124, 03/05/26; HR16524, 06/14/26; HR23624, 08/27/26; HR34124, 12/11/26; HR07125, 03/13/27; HR09025, 04/03/27; HR23425, 08/27/27; HR34425, 12/15/27; HR01926, 01/28/28.
    Where it was sold
    Domestic distribution: AK, AL, AR, AZ, CA, CO, FL, IA, ID, IL, IN, KS, LA, MI, MN, MO, MT, NE, NM, NV, OH, OK, OR, TN, TX, UT, VA, WA, WI. Foreign distribution: Canada, Japan.
    Amount recalled
    2,494 cases (25 lbs/case)
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0672-2026
    View in FDA's recall database
  6. ACTIVEClass II · ModerateRecalled Apr 7, 2026

    EL MEXICANO horchata casera Instant Horchata Drink NET WT 14oz (396g) INGREDIENTS: *** MILK SUBSTITU...

    Undeclared milk.

    Marquez Brothers International, Inc. · Fresno, CA

    Where it was sold: Domestic distribution: AK, AL, AR, AZ, CA, CO, FL, IA, ID, IL, IN, KS, LA, MI, MN, MO, MT, NE, NM, NV, OH, OK, OR, TN, TX, UT, VA, WA, WI. Foreign distribution: Canada, Japan.

    UPC 042743190266
    Show details
    Product, as FDA describes it
    EL MEXICANO horchata casera Instant Horchata Drink NET WT 14oz (396g) INGREDIENTS: *** MILK SUBSTITUTE (WHEY *** LACTOSE *** DISTRIBUTED BY MARQUEZ BROTHERS INTERNATIONAL, INC. San Jose CA 95138 UPC: 042743190266 Item: 102284
    Reason, in FDA's words
    Undeclared milk.
    Codes on the package
    Lot, Expiration: HC10124, 04/11/26; HC16524, 06/14/26; HC21324, 08/01/26; HC29924, 10/28/26; HC06625, 03/06/27; HC06625, 03/07/27; HC16325, 06/13/27; HC19525, 07/15/27; HC28325, 10/13/27; HC28325, 10/14/27.
    Where it was sold
    Domestic distribution: AK, AL, AR, AZ, CA, CO, FL, IA, ID, IL, IN, KS, LA, MI, MN, MO, MT, NE, NM, NV, OH, OK, OR, TN, TX, UT, VA, WA, WI. Foreign distribution: Canada, Japan.
    Amount recalled
    40,032 packages (16 packages/case; 2,502 cases)
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0673-2026
    View in FDA's recall database
  7. ACTIVEClass II · ModerateRecalled Apr 7, 2026

    EL MEXICANO agua fresca de horchata Instant Horchata Drink NET WT 12oz (340g) INGREDIENTS: *** MILK ...

    Undeclared milk.

    Marquez Brothers International, Inc. · Fresno, CA

    Where it was sold: Domestic distribution: AK, AL, AR, AZ, CA, CO, FL, IA, ID, IL, IN, KS, LA, MI, MN, MO, MT, NE, NM, NV, OH, OK, OR, TN, TX, UT, VA, WA, WI. Foreign distribution: Canada, Japan.

    UPC 042743190204
    Show details
    Product, as FDA describes it
    EL MEXICANO agua fresca de horchata Instant Horchata Drink NET WT 12oz (340g) INGREDIENTS: *** MILK SUBSTITUTE (WHEY *** LACTOSE *** DISTRIBUTED BY MARQUEZ BROTHERS INTERNATIONAL, INC. San Jose CA 95138 UPC: 042743190204 Item: 102279
    Reason, in FDA's words
    Undeclared milk.
    Codes on the package
    Lot, Expiration: HR02324, 01/26/26; HR02324, 01/29/26; HR06424, 03/07/26; HR09924, 04/09/26; HR10024, 04/10/26; HR12924, 05/09/26; HR13024, 05/13/26; HR13024, 05/14/26; HR16424, 06/13/26; HR17824, 06/27/26; HR17824, 06/28/26; HR21124, 07/30/26; HR21224, 07/31/26; HR23524, 08/26/26; HR23624, 08/27/26; HR26724, 09/25/26; HR29724, 10/24/26; HR29824, 10/25/26; HR29924, 11/19/26; HR32424, 11/20/26; HR02225, 01/23/27; HR02225, 01/24/27; HR05825, 03/05/27; HR05925, 03/06/27; HR08625, 03/28/27; HR08625, 03/31/27; HR08725, 04/01/27; HR15725, 06/09/27; HR16025, 06/10/27; HR16225, 06/12/27; HR16325, 06/13/27; HR19125, 07/11/27; HR19225, 07/15/27; HR23325, 08/22/27; HR23225, 08/21/27; HR27925, 10/08/27; HR28225, 10/13/27; HR34425, 12/15/27; HR34525, 12/16/27.
    Where it was sold
    Domestic distribution: AK, AL, AR, AZ, CA, CO, FL, IA, ID, IL, IN, KS, LA, MI, MN, MO, MT, NE, NM, NV, OH, OK, OR, TN, TX, UT, VA, WA, WI. Foreign distribution: Canada, Japan.
    Amount recalled
    405,136 packages (16 packages/case; 25,321 cases)
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0674-2026
    View in FDA's recall database
  8. ACTIVEClass II · ModerateRecalled Apr 6, 2026

    Liquid Blenz Soursop Bitters 16 oz and 32 oz.

    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

    LIQUID BLENZ CORP · Rockville Centre, NY

    Where it was sold: NY and online sales

    UPC 860005735006UPC 860005735013
    Show details
    Product, as FDA describes it
    Liquid Blenz Soursop Bitters 16 oz and 32 oz.
    Reason, in FDA's words
    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
    Codes on the package
    16 oz with upc: 860005735006 & 32 oz with upc: 860005735013 Lots: SS75223, SS00669, SS95811, SS95114, SS11139, SS54495, SS81258, SS44886
    Where it was sold
    NY and online sales
    Amount recalled
    18,190 bottles total
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0782-2026
    View in FDA's recall database
  9. ACTIVEClass II · ModerateRecalled Apr 6, 2026

    Blackseed Bitters 16 oz and 32 oz.

    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

    LIQUID BLENZ CORP · Rockville Centre, NY

    Where it was sold: NY and online sales

    UPC 860005735020UPC 860005735037
    Show details
    Product, as FDA describes it
    Blackseed Bitters 16 oz and 32 oz.
    Reason, in FDA's words
    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
    Codes on the package
    16 oz. with upc: 860005735020 & 32 oz with upc: 860005735037 Lots: BS62367, BS25400, BS11595, BS75444, BS75721, BS90605, BS34888
    Where it was sold
    NY and online sales
    Amount recalled
    18,190 bottles total
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0783-2026
    View in FDA's recall database
  10. ACTIVEClass II · ModerateRecalled Apr 6, 2026

    Sea Moss Tonic 16 oz and 32. oz.

    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

    LIQUID BLENZ CORP · Rockville Centre, NY

    Where it was sold: NY and online sales

    UPC 196852654833UPC 196852456406
    Show details
    Product, as FDA describes it
    Sea Moss Tonic 16 oz and 32. oz.
    Reason, in FDA's words
    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
    Codes on the package
    16 oz with upc: 196852654833 & 32 oz with upc: 196852456406 Lots: not provided
    Where it was sold
    NY and online sales
    Amount recalled
    18,190 bottles total
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0784-2026
    View in FDA's recall database
  11. ACTIVEClass II · ModerateRecalled Apr 6, 2026

    Pure Diabetes Bully 16 oz and 32 oz.

    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

    LIQUID BLENZ CORP · Rockville Centre, NY

    Where it was sold: NY and online sales

    UPC 195893374878UPC 195893984466
    Show details
    Product, as FDA describes it
    Pure Diabetes Bully 16 oz and 32 oz.
    Reason, in FDA's words
    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
    Codes on the package
    16 oz with upc: 195893374878 & 32 oz with upc: 195893984466 Lots: DB58525, DB58885, DB21000, DB58661, DB25909, DB09550, DB66236, DB52855
    Where it was sold
    NY and online sales
    Amount recalled
    18,190 bottles total
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0785-2026
    View in FDA's recall database
  12. ACTIVEClass II · ModerateRecalled Apr 6, 2026

    Pure Libido Drink 16 oz and 32 oz.

    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

    LIQUID BLENZ CORP · Rockville Centre, NY

    Where it was sold: NY and online sales

    UPC 195893463176UPC 195893949991
    Show details
    Product, as FDA describes it
    Pure Libido Drink 16 oz and 32 oz.
    Reason, in FDA's words
    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
    Codes on the package
    16 oz with upc: 195893463176 & 32 oz with upc: 195893949991 Lots: LB08560, LB18863, LB76882, LB84633, LB55881
    Where it was sold
    NY and online sales
    Amount recalled
    18,190 bottles total
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0786-2026
    View in FDA's recall database
  13. ACTIVEClass II · ModerateRecalled Apr 6, 2026

    Immunity Enhancer Elderberry 16 oz and 32 oz.

    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

    LIQUID BLENZ CORP · Rockville Centre, NY

    Where it was sold: NY and online sales

    UPC 860005735099UPC 195893965434
    Show details
    Product, as FDA describes it
    Immunity Enhancer Elderberry 16 oz and 32 oz.
    Reason, in FDA's words
    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
    Codes on the package
    16 oz with upc: 860005735099 & 32 oz with upc: 195893965434 Lots: not provided
    Where it was sold
    NY and online sales
    Amount recalled
    18,190 bottles total
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0787-2026
    View in FDA's recall database
  14. ACTIVEClass II · ModerateRecalled Apr 6, 2026

    Menopause Bully 16 oz and 32 oz.

    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

    LIQUID BLENZ CORP · Rockville Centre, NY

    Where it was sold: NY and online sales

    UPC 860010984420UPC 860010984437
    Show details
    Product, as FDA describes it
    Menopause Bully 16 oz and 32 oz.
    Reason, in FDA's words
    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
    Codes on the package
    16oz with upc: 860010984420 & 32oz with upc: 860010984437 Lots: not provided
    Where it was sold
    NY and online sales
    Amount recalled
    18,190 bottles total
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0788-2026
    View in FDA's recall database
  15. ACTIVEClass II · ModerateRecalled Apr 6, 2026

    Fibroid Bully 16 oz and 32 oz.

    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

    LIQUID BLENZ CORP · Rockville Centre, NY

    Where it was sold: NY and online sales

    UPC 860010984406UPC 860010984413
    Show details
    Product, as FDA describes it
    Fibroid Bully 16 oz and 32 oz.
    Reason, in FDA's words
    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
    Codes on the package
    16 oz with upc: 860010984406 & 32 oz with upc: 860010984413 Lots: not provided
    Where it was sold
    NY and online sales
    Amount recalled
    18,190 bottles total
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0789-2026
    View in FDA's recall database
  16. ACTIVEClass II · ModerateRecalled Apr 6, 2026

    Prostate Bully 16 oz and 32 oz

    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

    LIQUID BLENZ CORP · Rockville Centre, NY

    Where it was sold: NY and online sales

    UPC 860010984444UPC 860010984451
    Show details
    Product, as FDA describes it
    Prostate Bully 16 oz and 32 oz
    Reason, in FDA's words
    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
    Codes on the package
    16 oz with upc: 860010984444 & 32 oz with upc: 860010984451 Lots: PB11333, PB29969, PB57444, PB00880, PB48552;
    Where it was sold
    NY and online sales
    Amount recalled
    18,190 bottles total
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0790-2026
    View in FDA's recall database
  17. ACTIVEClass II · ModerateRecalled Apr 6, 2026

    Pure Shilajit Tonic 16 oz and 32 oz

    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

    LIQUID BLENZ CORP · Rockville Centre, NY

    Where it was sold: NY and online sales

    UPC 860010984482UPC 860010984499
    Show details
    Product, as FDA describes it
    Pure Shilajit Tonic 16 oz and 32 oz
    Reason, in FDA's words
    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
    Codes on the package
    16 oz with upc: 860010984482 & 32 oz with upc: 860010984499 Lots: not provided
    Where it was sold
    NY and online sales
    Amount recalled
    18,190 bottles total
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0791-2026
    View in FDA's recall database
  18. ACTIVEClass II · ModerateRecalled Apr 6, 2026

    Blood Pressure Bully 16 oz and 32 oz

    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

    LIQUID BLENZ CORP · Rockville Centre, NY

    Where it was sold: NY and online sales

    UPC 196852985432UPC 196852553129
    Show details
    Product, as FDA describes it
    Blood Pressure Bully 16 oz and 32 oz
    Reason, in FDA's words
    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
    Codes on the package
    16 oz with upc: 196852985432 & 32 oz with upc: 196852553129 Lots: BP02581, BP83283, BP14888, BP95123, BP75660
    Where it was sold
    NY and online sales
    Amount recalled
    18,190 bottles total
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0792-2026
    View in FDA's recall database
  19. ACTIVEClass II · ModerateRecalled Apr 6, 2026

    Flat Belly Bully 16 oz and 32 oz

    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

    LIQUID BLENZ CORP · Rockville Centre, NY

    Where it was sold: NY and online sales

    UPC 196852337118UPC 196852926770
    Show details
    Product, as FDA describes it
    Flat Belly Bully 16 oz and 32 oz
    Reason, in FDA's words
    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
    Codes on the package
    16 oz with upc: 196852337118 & 32 oz with upc: 196852926770 Lots: : FBB5552, FBB6226, FBB8166, FBB8536, FBB7757, FBB5277
    Where it was sold
    NY and online sales
    Amount recalled
    18,190 bottles total
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0793-2026
    View in FDA's recall database
  20. ACTIVEClass II · ModerateRecalled Apr 6, 2026

    Liquid Blenz Good Brain Tonic 16 oz and 32 oz

    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

    LIQUID BLENZ CORP · Rockville Centre, NY

    Where it was sold: NY and online sales

    UPC 860010984468UPC 860010984475
    Show details
    Product, as FDA describes it
    Liquid Blenz Good Brain Tonic 16 oz and 32 oz
    Reason, in FDA's words
    May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
    Codes on the package
    16 oz with UPC: 860010984468 & 32 oz with UPC: 860010984475 Lots: not provided
    Where it was sold
    NY and online sales
    Amount recalled
    18,190 bottles total
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    H-0794-2026
    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.

At the store?

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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.