The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

11726–11750 of 53044

  • HighFDA (Devices)·Z-2517-2023·2023-09-13

    Philips 3D9-3v Ultrasound Transducer may separate due to bonding defect

    Philips 3D9-3v Transducer units may separate at the chassis bonding, risking electric shock and tissue damage if safety systems fail. Affected units distributed worldwide.

    Product
    3D9-3v Transducer, accessory to Philips Ultrasound Systems: EPIQ Elite; Affiniti 30, 50, and 70; ClearVue 850; HD15; iU22; and Compact 5000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2403-2023·2023-09-13

    Azurion imaging systems recalled for stuck foot switch causing unintended radiation

    Philips recalls Azurion imaging systems because the foot switch pedal may stick in the active position, causing unintended radiation emission. Facilities should stop using the systems and contact Philips for guidance.

    Product
    Azurion
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1170-2023·2023-09-13

    Digoxin Tablets Recalled Due to Reversed Dosage Labeling

    Marlex Pharmaceuticals is recalling Digoxin Tablets because bottles labeled as 0.125mg contain 0.25mg strength, and vice versa. Approximately 94 100-count bottles distributed nationwide are affected.

    Product
    Digoxin Tablets, USP 0.25mg, 100-count bottles, Rx Only, Manufactured for/Distributed by: Marlex Pharmaceuticals, Inc. New Castle, DE NDC 10135-0748-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-09132023-01·2023-09-13

    Kirkland Signature Chicken Tortilla Soup Recalled for Gluten Misbranding

    USDA FSIS issued a public health alert for Kirkland Signature Chicken Tortilla Soup labeled as gluten-free but containing gluten. No illnesses have been reported.

    Product
    Kettle Cuisine Midco, LLC — FSIS Issues Public Health Alert for Kirkland Signature Chicken Tortilla Soup Product Due to Misbranding
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-2402-2023·2023-09-13

    Philips Allura Xper X-ray Systems Foot Pedal May Stick, Causing Unintended Radiation

    Philips Allura Xper X-ray imaging systems are being recalled because the foot switch pedal may become stuck in the active position, potentially causing unintended radiation emission. The recall affects 5,432 systems distributed nationwide.

    Product
    Allura Xper series
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2523-2023·2023-09-13

    Reusable Endoscopy Distal Attachments Recalled for Excessive DEHP Levels

    Aomori Olympus recalls 1,252 reusable distal attachment devices with DEHP chemical levels exceeding safe exposure limits per medical device standards. Devices distributed nationwide in the United States.

    Product
    Reusable distal attachments Models: MH-462, MH-463, MH-464, MH-465, MH-466, MH-483, MH-587, MH-588(US), MH-589, MH-590, MH-591, MH-592, MH-593, MH-594, MH-595, MH-596, MH-597, MH-598, MAJ-289, MAJ-290, MAJ-291, MAJ-292, MAJ-293, MAJ-294, MAJ-295, MAJ-296, MAJ-297, MAJ-663…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1490-2023·2023-09-13

    Cooperstown Cheese Company multiple cheese products recalled for Listeria risk

    Cooperstown Cheese Company recalled 12 cheese varieties distributed in New York due to potential Listeria monocytogenes contamination. Consumers should not consume affected products.

    Product
    Cooperstown Cheese Company 1. Jersey Girl 2. Toma Celena 3. Abbie 4. SK 5. Jersey Girl with garlic/rosemary 6.Jersey Girl spring onion 7. Bobby s got the Blues 8.Toma Torino 9. Jersey Gold with garlic 10. Abbie. 11. Jersey Gold 12. Marielle
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2404-2023·2023-09-13

    Medical Imaging System Recalled for Foot Pedal Malfunction Risk

    Philips MultiDiagnost-Eleva imaging systems may emit unintended radiation if the foot pedal gets stuck in the active position. The FDA is alerting healthcare facilities to this potential equipment malfunction.

    Product
    MultiDiagnost-Eleva
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V209000·2023-09-13

    School buses recalled for automatic electrical disconnect switch failure

    Certain 2021-2023 Thomas Built school buses may lose critical driving functions due to automatic electrical switch failure. Dealers will remove the faulty switch at no cost.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2522-2023·2023-09-13

    Olympus Distal Attachment Recalled for Phthalate Exceeding Permissible Levels

    Aomori Olympus Co., Ltd. recalls 1,048 Olympus Distal Attachment units used in EMR kits due to di-2-ethylhexyl phthalate (DEHP) exceeding permissible exposure limits per ISO 10993-17: 2002. Devices were distributed nationwide.

    Product
    Olympus Distal Attachment (in Olympus Disposable EMR Kit)- Designed to be attached to the distal end of the endoscope. Disposable EMR Kit: K-001, K-002, K-003, K-004, K-011, K-012
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1491-2023·2023-09-13

    Nestle Toll House Cookie Dough Recalled for Potential Wood Fragments

    Nestle USA is recalling Toll House Chocolate Chip Cookie Dough due to potential wood fragments. The recall affects 147,816 packages distributed across multiple U.S. states.

    Product
    Nestle Toll House, Chocolate Chip Cookie Dough, 16.5 oz. Cookie dough in bar form packaged in paperboard tray with plastic overwrap, 12 packages per case, Keep Refrigerated
    Category
    Food
    Distribution
    28 states
  • HighNHTSA·23V631000·2023-09-12

    Spartan Fire Recalls Emergency Vehicles Due to Parking Brake Defect

    Spartan Fire is recalling 660 emergency vehicles because a parking brake defect may allow the vehicle to move unintentionally.

    Product
    SPARTAN FIRE — SPARTAN FIRE, KME GLADIATOR, FC-94, METROSTAR, redundant PREDATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V632000·2023-09-12

    Kentucky Trailer XL-12 Recalled for Refrigeration Unit Fire Risk

    Kentucky Trailer is recalling 2019-2023 XL-12 trailers because a refrigeration unit clutch may overheat and break, posing a fire risk.

    Product
    KENTUCKY TRAILER — KENTUCKY TRAILER XL-12
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V630000·2023-09-11

    2021-2022 Genesis vehicles fuel pump failure increases crash risk

    Hyundai is recalling certain 2021-2022 Genesis G80, GV80, and GV70 vehicles due to potential fuel pump failures that may cause loss of drive power and increase crash risk. Dealers will replace the fuel pump free of charge.

    Product
    GENESIS — GENESIS G80, GV80, GV70
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V628000·2023-09-08

    Nissan Altima and Sentra rearview camera harness defect increases crash risk

    Nissan is recalling certain 2019-2021 Altima and 2020-2021 Sentra vehicles because the rearview camera harness can become damaged, preventing the camera display from working. This reduces rear visibility and increases the risk of crashes when backing.

    Product
    NISSAN — NISSAN SENTRA, ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23790·2023-09-07

    ARGO Xplorer ATVs Recalled for Fire Hazard from Fuel Overflow

    ARGO USA Inc. is recalling about 500 ARGO Xplorer ATVs due to incorrectly installed check valves and vent hoses that can cause fuel overflow and pose a fire hazard. The firm has received two reports of fuel overflow incidents, including one fire, with no injuries reported.

    Product
    ARGO Xplorer ATVs
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23791·2023-09-07

    Whirlpool ADC Commercial Clothes Dryers Recalled for Fire Hazard

    Whirlpool has recalled about 2,500 ADC brand 30 lb. capacity stacked commercial clothes dryers because they can overheat and ignite clothes, creating a fire hazard. The company has received two reports of fuel overflow incidents, including one fire, with no injuries reported.

    Product
    ADC brand 30 lb. capacity stacked commercial clothes dryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23276·2023-09-07

    Pirelli P ZERO Race TLR Bicycle Tires Recalled for Fall Hazard

    Pirelli is recalling about 14,500 P ZERO Race TLR bicycle tires because the tire bead can unseat from the rim, causing rapid air loss and loss of control. Consumers should stop using the tires and contact Pirelli for a free replacement or refund.

    Product
    Pirelli P ZERO Race TLR Bicycle Tires
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V622000·2023-09-07

    2023-2024 BMW Models Recall: Front Passenger Knee Air Bag Deployment Failure

    BMW is recalling certain 2023 BMW XM and 2024 BMW X5, X6, X7, and Alpina XB7 vehicles because the front passenger knee air bag may not deploy as intended, increasing injury risk in a crash.

    Product
    BMW — BMW X6, XM, X5, X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23789·2023-09-07

    Lectric eBikes Disc Brake Calipers Recalled for Crash and Injury Hazards

    Lectric eBikes is recalling about 45,000 disc brake calipers on certain e-bicycle models because the brakes can fail, causing loss of control and crashes. The firm has received four reports of lost braking power, including two injuries.

    Product
    Disc brake calipers sold on Lectric e-bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23274·2023-09-07

    Emporia Smart Plugs Recalled Due to Electric Shock Hazard

    Emporia Energy Corp. is recalling about 80,000 smart plugs sold online from July 2022 through May 2023 because they are not adequately grounded and can pose an electric shock hazard.

    Product
    Emporia Smart Plugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1114-2023·2023-09-06

    Neonatal TPN Starter Bag recalled for sterility assurance concerns

    Central Admixture Pharmacy Services is recalling a neonatal TPN bag due to lack of validated sanitation cycles, affecting 84 units distributed nationwide.

    Product
    Neonatal TPN Starter Bag, Amino Acids (Trophamine) 2.5%/Dextrose 10% with CALCIUM and HEPARIN, total volume = 250mL, EVA Bag, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0418-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2498-2023·2023-09-06

    Olympus Bronchovideoscope Recalled Due to Lodging Risk in Airway

    Olympus is recalling Bronchovideoscope Model BF-XT190 units because the device diameter is too large, causing the endoscope to become lodged in endotracheal tube connectors.

    Product
    Olympus Bronchovideoscope, Models BF-XT190.
    Category
    Medical Device
    Distribution
    Distributed nationwide