The Recall Desk

Severity 4 of 5

Severe recalls

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

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.

5001–5025 of 29102

  • SevereNHTSA·23V430000·2023-06-15

    2023 Honda Civic recalled for brake modulator fluid leak

    Honda recalls 2023 Civic vehicles with a defective brake modulator that may leak fluid, potentially causing unintended vehicle movement or increased brake pedal travel.

    Product
    HONDA — HONDA, ACURA ACCORD, INTEGRA, RDX, CIVIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1649-2023·2023-06-14

    Philips Respironics Ventilators Recalled for Flow Sensor Debris Accumulation

    Philips Respironics recalled approximately 57,395 ventilators due to environmental debris potentially accumulating on the flow sensor, which may prevent accurate delivery of pressure and volume to patients, risking hypoxemia.

    Product
    Trilogy Evo, Garbin Evo, and Aeris EVO, Model Numbers DS2110X11B, IN2110X15B, JP2110X16B, AU2110X15B, LA2110X15B, CA2110X12B, BR2110X18B, KR2110X15B, IA2110X15B, FP2110X10, FR2110X14B, ND2110X15B, IT2110X21B, ES2110X15B, DE2110X13B, BL2110X15B, GB2110X15B, EU2110X15B, EE2110X15B,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1630-2023·2023-06-14

    StealthStation Cranial Software Depth Gauge Synchronization Failure Risk

    A software anomaly in StealthStation Cranial Software causes depth gauge displays to lose synchronization during cranial biopsy procedures, risking inaccurate surgical guidance and tissue injury.

    Product
    StealthStation Cranial Software, Models: 9735585, 9735586 (kit), 9735587 (kit), used with StealthStation S7/i7 systems
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0979-2023·2023-06-14

    TETAS Mireya Galleta Maria Cookies Recalled for Undeclared Soy and Wheat

    DIBE LLC is recalling TETAS Mireya SABOR Galleta Maria cookies due to undeclared soy and wheat allergens. Consumers with allergies to these ingredients should not consume the product.

    Product
    TETAS Mireya, SABOR Galleta Maria
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0975-2023·2023-06-14

    Food Recall: Meijer Express Dark Chocolate Covered Almonds Due to Undeclared Milk

    Meijer Inc is recalling Meijer Express Dark Chocolate Covered Almonds due to undeclared milk, a serious risk for consumers with milk allergies. The recall affects 9,030 units in Michigan, Indiana, Illinois, Ohio, Kentucky, and Wisconsin.

    Product
    Meijer Express Dark Chocolate Covered Almonds, 7.5oz plastic cup with lid, UPC 7-60236-19787-4
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1651-2023·2023-06-14

    Trilogy Evo O2 EV300 respiratory devices recalled for debris accumulation

    Philips Respironics recalled 18,855 Trilogy Evo O2 EV300 devices because environmental debris may accumulate on the flow sensor, potentially causing inaccurate delivery of pressure or flow. This could result in patient hypoxemia if not promptly addressed.

    Product
    Trilogy Evo O2 EV300, Model Numbers DS2200X11B, IN2200X15B, FX2200X15B, CA2200X12B, FR2200X14B, ND2200X15B, ES2200X15B, BL2200X15B, GB2200X15B, EU2200X15B, EE2200X15B, and TR2200X15B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V427000·2023-06-14

    Great Dane Recalls 2024 Trailers Due to Tire Pressure Loss Risk

    Great Dane is recalling 2024 Champion and Everest trailers because tire pressure may drop at speeds over 45 mph, increasing crash risk.

    Product
    GREAT DANE — GREAT DANE EVEREST, CHAMPION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0977-2023·2023-06-14

    Onion Powder Premium Recalled for Potential Salmonella Contamination

    Olam Food Ingredients is recalling Onion Powder Premium sold in bulk fiber bags due to potential Salmonella contamination. Affected product was distributed to Canada, Arkansas, and Illinois.

    Product
    Onion Powder Premium, 44.9 and 50 lb. fiber bags sold as bulk ingredient
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-1633-2023·2023-06-14

    FDA Recalls Walnut Wearable Smart Thermometer Due to Reported Skin Burns

    BearCare's Walnut Wearable Smart Thermometer (Model WT20) is being recalled due to reports of skin burns in children ages 0-6. The device was distributed nationwide; 1818 units were affected.

    Product
    Walnut Wearable Smart Thermometer, intended for continuous chest temperature monitoring of children ages 0-6 years in non-emergency medical situations, Model Number WT20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1652-2023·2023-06-14

    Trilogy Evo Universal Ventilator Class I Recall—22,237 Units Affected

    The FDA has issued a Class I recall for the Trilogy Evo Universal Ventilator Model DS2000X11B, affecting 22,237 units distributed nationwide and globally. The device is manufactured by Philips Respironics, Inc.

    Product
    Trilogy Evo Universal Ventilator, Model Number DS2000X11B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0974-2023·2023-06-14

    Dark Chocolate Almonds Recalled Due to Undeclared Milk Allergen

    Meijer Inc is recalling Frederik's by Meijer Dark Chocolate Almonds due to undeclared milk. The product was distributed to Meijer stores in six Midwest states.

    Product
    Frederik's by Meijer Dark Chocolate Almonds, 12oz stand-up pouch, UPC 7-08820-68730-1
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0980-2023·2023-06-14

    TETAS Mireya candy recalled for undeclared soy and walnut allergens

    DIBE LLC is recalling TETAS Mireya candy due to undeclared soy and walnut allergens. Consumers with allergies to these ingredients should not consume the product.

    Product
    TETAS Mireya, SABOR Ferrero
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·23V425000·2023-06-13

    Blue Bird Recalls School Buses Due to Air Brake Warning Failure

    Blue Bird is recalling 2021-2024 All American and 2021-2022 Vision school buses because a software error may prevent air pressure warnings from functioning, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V424000·2023-06-13

    Blue Bird Recalls 2022-2024 All American Transit Buses for Brake Warning Defect

    Blue Bird is recalling 2022-2024 All American transit buses because a software error may prevent air pressure gauges and low air warnings from functioning, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V421000·2023-06-12

    2022 Nissan Sentra: Driver Cowl Seal Defect May Cause Electrical Failures

    The 2022 Nissan Sentra may have a defective driver's side cowl seal, allowing water intrusion and electrical corrosion. This could cause loss of airbag function, exterior lighting, and braking safety features, increasing crash and fire risk.

    Product
    NISSAN — NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·022-2023·2023-06-09

    J.T.M. Provisions Recalls Homestyle Chili Topping for Undeclared Soy Allergen

    J.T.M. Provisions is recalling approximately 200 pounds of ready-to-eat Homestyle Chili Topping because it may contain beef taco filling with undeclared soy.

    Product
    J.T.M. Provisions Company — J.T.M. Provisions Company Recalls Ready-To-Eat Homestyle Chili Topping Product Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V413000·2023-06-08

    Jeep Grand Cherokee Models Recalled for Detaching Rear Coil Springs

    Chrysler is recalling certain 2022-2023 Jeep Grand Cherokee and 2021-2023 Jeep Grand Cherokee L vehicles. Rear coil springs may detach while driving, creating a crash risk; dealers will repair them free.

    Product
    JEEP — JEEP GRAND CHEROKEE 4XE, GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V411000·2023-06-08

    Chrysler Recalls Jeep and Ram Vehicles for Engine Stall Risk

    Chrysler is recalling 2014-2020 Jeep Grand Cherokee and 2014-2019 Ram 1500 vehicles with 3.0L Diesel engines because a sensor defect may cause the engine to stall, increasing crash risk.

    Product
    JEEP — JEEP, RAM GRAND CHEROKEE, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V417000·2023-06-08

    Altec Recalls 2022-2023 TG-124S Trailers Due to Loose Axle U-Bolts

    Altec is recalling 2022-2023 TG-124S trailers because axle U-bolts may loosen and detach, increasing crash risk. Owners should contact Altec for a free inspection and tightening.

    Product
    ALTEC — ALTEC TG-124S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0963-2023·2023-06-07

    Bean Sprouts from Chang & Son Enterprises Recalled for Listeria Contamination

    Bean sprouts produced by Chang & Son Enterprises, Inc. are recalled due to potential Listeria monocytogenes contamination. Affected products include 10-pound bags and 12-ounce packages with sell-by dates before May 28, 2023.

    Product
    a.) BEAN SPROUTS, 10 LBS, PRODUCT OF USA; CHANG FARM; SO.DEERFIELD, MA; KEEP REFRIGERATED; package in plastic bags b.) Nature's Wonder brand Premium BEAN SPROUTS; ALL NATURAL AND READY TO COOK; NET WT 12 oz (340 g); REFRIGERATE
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-0964-2023·2023-06-07

    Soybean Sprouts Recalled Due to Potential Listeria Contamination

    Nature's Wonder Premium Soybean Sprouts are recalled due to potential Listeria monocytogenes contamination. Affected products (12 oz bags, UPC 815098001347) were distributed in seven states; discard or return if purchased.

    Product
    Nature's Wonder Premium Soybean Sprouts 12oz bag (UPC: 815098001347)
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0868-2023·2023-06-07

    Pediatric Cough Suppressant G-SUPRESS DX Recalled Due to Product Mix-Up

    G-SUPRESS DX pediatric drops are being recalled due to a product mix-up: an incorrect product was found inside some cartons in Puerto Rico. The recall affects 9,077 bottles (Lot D20911, expires Oct/25).

    Product
    G-SUPRESS DX — G-SUPRESS DX (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-0970-2023·2023-06-07

    Organic Pineapple Chunks Recalled for Potential Listeria Contamination

    SunOpta Grains and Foods Inc. is recalling Organic Pineapple Chunks due to potential Listeria monocytogenes contamination. Affected lots 8FQ229702000MX and 8FQ229802000MX were distributed in Oregon.

    Product
    Organic Pineapple Chunks, Item 4510-000, packed in 30 lb. poly-lined boxes.
    Category
    Food
    Distribution
    1 state