The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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13951–13975 of 27735

  • HighCPSC·24740·2024-02-22

    Polaris MATRYX Snowmobiles Recalled for Primary Clutch Failure Hazard

    Polaris is recalling Model Year 2022–2024 MATRYX snowmobiles with PATRIOT 650 and 850 engines because the primary clutch can fail and separate from the vehicle, creating an injury hazard. Polaris has received 109 reports of clutch failure, including one incident resulting in a laceration injury.

    Product
    Model Year 2022-2024 MATRYX Snowmobiles equipped with PATRIOT 650 and 850 Engines
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24738·2024-02-22

    Magik & Kover Pack and Play Mattresses Recalled for Suffocation Hazard

    Magik & Kover Pack and Play Mattresses sold on Amazon are being recalled because they violate federal safety regulations for crib mattresses and pose a suffocation hazard to infants. Consumers should immediately stop using the mattresses and contact the company for a refund.

    Product
    Magik & Kover Pack and Play Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24124·2024-02-22

    EVAS 20-lb Propane Exchange Cylinders Recalled for Fire Hazard

    Worthington Enterprises is recalling about 146,160 EVAS 20-lb propane exchange cylinders that could leak gas and pose a fire hazard. Consumers should stop using them immediately and return them to AmeriGas for free replacement.

    Product
    EVAS 20-lb. propane exchange cylinders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0868-2024·2024-02-21

    Al Amir Fresh Foods Hummus recalled for undeclared sesame allergen

    Al Amir Fresh Foods Harissa Spicy Hummus With a Kick is being recalled due to an undeclared sesame allergen. The product declares tahini but not sesame, which could cause serious allergic reactions in people with sesame sensitivity.

    Product
    Al Amir Fresh Foods Harissa Spicy Hummus With a Kick, packaged in round plastic clear container, net wt. 8oz. There are 12 containers per case. UPC on 8oz container: 7 55134 12352 0. The recalled product label declares: Ingredients: Garbanzo Beans, Tahini Paste, Garlico (Fresh G
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0874-2024·2024-02-21

    Mighty Fine Chocolate Ice Cream Recalled for Undeclared Peanuts

    Byrne Dairy, Inc is recalling Mighty Fine Chocolate Ice Cream because it contains undeclared peanuts. Consumers with peanut allergies should not consume this product.

    Product
    Mighty Fine Chocolate Ice Cream
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0867-2024·2024-02-21

    Al Amir Fresh Foods Hummus Recalled for Undeclared Sesame Allergen

    Al Amir Fresh Foods Classic Hummus Creamy Garbanzo is recalled because it contains sesame (tahini) but the label does not declare sesame as an allergen. Consumers with sesame allergies may experience allergic reactions.

    Product
    Al Amir Fresh Foods Classic Hummus Creamy Garbanzo, packaged in round plastic clear container, net wt. 8oz. There are 12 containers per case. UPC on 8oz container: 7 55134 12341 4. The recalled product label declares: Ingredients: Garbanzo Beans, Tahini Paste, Garlico (Fresh G
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0875-2024·2024-02-21

    Fresh Express Chopped Salad Kit Southwest Recalled for Listeria Risk

    Fresh Express Incorporated is recalling Chopped Salad Kit Southwest products due to potential Listeria monocytogenes contamination in the cheese condiment pack. Consumers should not consume the product.

    Product
    Chopped Salad Kit Southwest with condiments(toppings that include cheese), labeled salad bag (Green Cabbage, Green Leaf Lettuce, Kale, Red Cabbage, Carrots, Green Onions, Tortilla Strips, Cheddar Cheese, and Chipotle Ranch Dressing), Net Wt 13.4 oz, 6 bags per case. UPC 681131305
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-0962-2024·2024-02-21

    GE Healthcare Lullaby Incubator bedside panels may fail to latch properly

    GE Healthcare Lullaby Incubator bedside panels and portholes may appear closed but not be properly latched. If impacted, these panels can disengage and fall open, creating a fall risk for patients.

    Product
    GE Healthcare Lullaby Incubator Model Hood Door FRU kit, Part Numbers: M1169767, M1160674, M1187512, M1206646, M1166822
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0959-2024·2024-02-21

    GE Healthcare Care Plus Incubator Hood Latching Defect Increases Fall Risk

    GE Healthcare incubator hoods can appear closed but may not be properly latched, posing a fall risk if patients impact an unsecured panel.

    Product
    GE Healthcare Care Plus Hood Field Replacement Unit (FRU) kit, Part Numbers: 6600-0047-851, 6600-0033-850, 6600-0081-850, 6600-0961-500, 6600-0083-850
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0958-2024·2024-02-21

    GE Healthcare Care Plus and Lullaby incubators recalled for bedside panel latching defect

    GE Healthcare is recalling 1,410 neonatal incubators worldwide because bedside panels and portholes can appear closed while not properly latched. If impacted, they may fall open and fail to protect patients from falls.

    Product
    GE Healthcare neonatal incubator, models: a) Lullaby Incubator, b) Lullaby Incubator XP, c) Lullaby Incubator TR
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0865-2024·2024-02-21

    Dragonfly Jelly Bar Handbags and Backpacks Recalled for Choking Hazard

    U.S. Tov, Inc. is recalling Dragonfly Jelly Bar Handbags and Backpacks due to a potential choking hazard from konjac. The products were distributed nationwide.

    Product
    Dragonfly Jelly Bar Handbag 11.64oz, 17.63oz UPC Code 721557357156, 721557357163 Dragonfly Jelly Bar Backpack 7.93oz, 28.22oz UPC Code 721557357170, 721557357187
    Category
    Food
    Distribution
    38 states
  • SevereFDA (Food)·F-0876-2024·2024-02-21

    Fresh Express Salad Kit Recalled for Potential Listeria Contamination

    Fresh Express Kit Salsa! Ensalada salad kits are recalled for potential Listeria monocytogenes contamination in the cheese condiment. The affected 12.1 oz bags were distributed to AL, FL, GA, CA, UT, WA, and Canada.

    Product
    Fresh Express Kit Salsa! Ensalada with condiments(toppings that include cheese), labeled salad bag (Iceberg & Romaine Lettuce, Salsa Ranch Dressing, Nacho Taco Seasoned Cheese Yellow & Blue Tortilla Strips), Net Wt 12.1 oz, 6 bags per case. UPC 071279309026
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-0961-2024·2024-02-21

    GE Healthcare Incubators Bedside Panel Latch Failure Poses Fall Risk

    GE Healthcare incubators have defective bedside panels that may appear closed but not be properly latched, creating a patient fall risk when the panels disengage upon impact.

    Product
    GE Healthcare Lullaby Incubator Model Hood FRU kit, Part Numbers: M1169566, M1160659, M1206259, M1206260, M1166836, M1166814
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0957-2024·2024-02-21

    GE Healthcare neonatal incubator bedside panels may fail to latch properly

    GE Healthcare is recalling neonatal incubators because the bedside panel can appear closed while unlatched. Impact could cause it to fall open, risking patient injury.

    Product
    GE Healthcare neonatal incubator, models: a) Care Plus, b) Care Plus 1000, c) Care Plus 2000, d) Care Plus 3000, e) Care Plus 4000, Plus 4000
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0903-2024·2024-02-21

    Mexican Style Quinoa Salad Recalled for Undeclared Soy and Egg Allergens

    Hans Kissle Company is recalling Mexican Style Quinoa Salad due to undeclared soy and egg allergens. The product was distributed in the Northeast and may pose serious risk to consumers with allergies.

    Product
    MEXICAN STYLE QUINOA SALAD
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0869-2024·2024-02-21

    Al Amir Baba Ghannooj Recalled for Undeclared Sesame Allergen

    Al Amir Fresh Foods Baba Ghannooj Grilled Eggplant is recalled for undeclared sesame. The product contains tahini but the label does not list sesame as an ingredient, posing a risk to consumers with sesame allergies.

    Product
    Al Amir Fresh Foods Baba Ghannooj Grilled Eggplant, packaged in round plastic clear container, net wt. 8oz. There are 12 containers per case. UPC on 8oz container: 7 55134 12342 1. The recalled product label declares: Ingredients: Fresh Grilled Eggplant, Tahini Paste, Garlico (F
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0866-2024·2024-02-21

    Utz Wavy Originals Potato Chips recalled for undeclared milk allergen

    Utz Wavy Originals Potato Chips (2.75 oz) distributed in New York may contain undeclared milk and could pose a risk to people with milk allergies.

    Product
    Utz Wavy Originals Potato Chips, Net WT. 2.75 oz (78g), UPC 0-41780-19014-7.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0960-2024·2024-02-21

    GE Healthcare incubator bedside panel may disengage and fall open

    The bedside panel on GE Healthcare Care Plus incubators may appear closed while unlatched. If impacted, the panel can fall open, exposing patients to injury risk.

    Product
    GE Healthcare Care Plus Hood Door FRU kit, Part Numbers: 6600-0082-850, 6600-0504-800, 6600-0148-800, and 6600-0970-500
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0980-2024·2024-02-21

    Impella Cardiac Support Catheters: Risk of Left Ventricle Perforation

    Impella cardiac catheters are being recalled due to risk of left ventricle perforation during operator use. The FDA has classified this Class I recall affecting 91,914 units worldwide.

    Product
    Impella catheters - Intravascular micro axial blood pumps that support a patient's circulatory system. (1) Product Code 005042 - Impella 2.5 (2) Product Code 005062 - Impella 5.0 (3) Product Code 005082- Impella LD (7) Product Codes 0550-0008 and 1000100 - Impella 5.5 wit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1075-2024·2024-02-21

    Medical Device Control Panel Contaminated with Norovirus, Causes False Positive Results

    Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet) negative control is contaminated with Norovirus. Users testing this control will incorrectly receive positive Norovirus results.

    Product
    Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet), REF 8184.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1066-2024·2024-02-21

    Bone Filler Tubes Recalled Due to Manufacturing Process Defect

    The FDA is recalling 89 AFT Bone Filler Tubes due to a manufacturing process defect that could cause extrudability issues during surgery. The filling process did not demonstrate adequate capability.

    Product
    AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1085-2024·2024-02-21

    Stryker Trevo Trak 21 Microcatheter Recalled for Unevaluated Intended Use

    Stryker, Inc. is recalling 63 units of the Trevo Trak 21 Microcatheter because the device instructions contain an intended use that has not been evaluated by the FDA.

    Product
    Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1089-2024·2024-02-21

    global Medium embryo culture media recalled for potential development impairment

    CooperSurgical is recalling three specific lots of global Medium embryo culture media distributed to fertility clinics worldwide due to performance issues that may impair embryo development during culture.

    Product
    global Medium, Model Numbers LGGG-020 (20mL bottle), LGGG-050 (50mL bottle), LGGG-100 (100mL bottle). Intended use: Culture of human embryos from zygote to blastocyst, embryo transfer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1074-2024·2024-02-21

    Impella Catheters: Warnings Added for Potential Fiber Ingestion Risk

    Abiomed is adding safety warnings to Instructions for Use for all Impella catheter models to prevent fibers from entering the device, which could result in reduced flow. The warning applies to all Impella models distributed worldwide.

    Product
    Impella catheters - Intravascular micro axial blood pumps that support a patient's circulatory system. (1) Product Code 005042 - Impella 2.5 (2) Product Code 005062 - Impella 5.0 (3) Product Code 005082- Impella LD (4) Product Code 004334 - Impella RP (5) Product Code 0046-0035
    Category
    Medical Device
    Distribution
    Distributed nationwide