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.

44401–44425 of 50511

  • HighNHTSA·12V572000·2012-12-11

    Daimler Recalls Thomas Built Buses Due to Fan Pulley Fatigue Risk

    Daimler Trucks North America is recalling 2011-2013 Thomas Built Buses equipped with specific Cummins diesel engines because a fan pulley can fail, causing engine overheating and potential vehicle disablement.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·13064·2012-12-11

    Fu San Machinery Recalls Low Lead Ball Valves Due to Fire Hazards

    Fu San Machinery is recalling approximately 163,000 low lead ball valves installed in flammable gas lines because they can crack and leak gas, posing fire and explosion risks.

    Product
    Low Lead Ball Valve/Shut-Off Gas Valves
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·12V570000·2012-12-11

    Thomas Built School Buses Recalled for Engine Fan Pulley Defect

    Daimler Trucks North America is recalling 2011-2013 Thomas Built school buses equipped with specific Cummins diesel engines due to a fan pulley defect that can cause engine overheating and vehicle disablement.

    Product
    THOMAS BUILT — THOMAS BUILT, THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V579000·2012-12-10

    Spartan Emergency Chassis Recalled for Wiper Motor Shaft Defect

    Spartan Chassis is recalling 2012-2013 emergency rescue chassis cabs because wiper motor and arm shafts have different sized splines, which may cause windshield wipers to become inoperative.

    Product
    SPARTAN — SPARTAN METROSTAR, GLADIATOR, FORCE, METROSTAR-X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V567000·2012-12-07

    Hyundai Recalls 2012 Veloster Vehicles Due to Parking Brake Binding

    Hyundai is recalling 2012 Veloster vehicles with manual transmissions because parking brake components may bind, potentially causing the vehicle to move unintentionally.

    Product
    HYUNDAI — HYUNDAI VELOSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V568000·2012-12-07

    Hyundai Recalls 2012 Veloster Vehicles Due to Sunroof Defect

    Hyundai is recalling 2012 Veloster vehicles with panoramic sunroofs because the glass assembly may be weakened, posing a risk of breakage while driving.

    Product
    HYUNDAI — HYUNDAI VELOSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V564000·2012-12-06

    Prevost Recalls 2011-2012 X3-45 Coach Buses Due to Fire Suppression Defect

    Prevost is recalling 87 model year 2011-2012 X3-45 coach buses because high engine temperatures may cause the fire suppression system to release prematurely, potentially preventing it from operating during a fire.

    Product
    PREVOST — PREVOST X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·13710·2012-12-06

    Grandin Road Recalls Metal Chairs Due to Fall Hazard

    Grandin Road is recalling about 2,200 metal chairs because the back legs can bend when a person leans back, posing a fall and injury hazard.

    Product
    Metal Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·12V565000·2012-12-06

    Spartan Recalls 2013 Motorhome Chassis Due to Brake Hose Damage Risk

    Spartan Chassis is recalling 2013 K2, K3, and MM motorhome chassis because front brake hoses or ABS sensor cables may be damaged by the swaybar, potentially increasing stopping distances or disabling ABS.

    Product
    SPARTAN — SPARTAN MM, K3, K2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·13059·2012-12-06

    Ridgid Pneumatic Nailers Recalled Due to Laceration Hazard

    One World Technologies is recalling Ridgid pneumatic nailers sold at Home Depot because the trigger assembly can malfunction and discharge fasteners, posing an injury risk.

    Product
    RIDGID Coil Roofing Nailer and RIDGID Clipped Head Framing Nailer
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-071-2013·2012-12-05

    Ranbaxy Recalls Atorvastatin Calcium Tablets Due to Glass Particulates

    Ranbaxy Inc. is recalling certain lots of Atorvastatin Calcium tablets because they may contain small glass particulates.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0728-2013·2012-12-05

    Mercer's Ice Cream Recalled for Undeclared Soy Allergen

    Quality Dairy Farms Inc. is recalling Mercer's Ice Cream Cookies 'N Cream because the product contains soy lecithin but the label only lists lecithin.

    Product
    Mercer's Ice Cream Cookies 'N Cream, Half Gallon (1.89 Liter), UPC 036667 200392
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0441-2013·2012-12-05

    Medtronic Recalls Vertex Max Drill Tubes Due to Threading Defect

    Medtronic is recalling 12 Vertex Max Drill Tubes due to a defect in the internal threading used for component setup.

    Product
    The Vertex Max Drill Tube is a component within the Navigated Vertex Max Drill Guide Set (item 9733370). The Navigated Vertex Max Drill Guide Set is intended to be used with a Medtronic Computer Assisted Surgery System to help assist with screw placement during spine surgical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0443-2013·2012-12-05

    Parks Medical Electronics Recalls Vascular Blood Flow Machines Due to Connection Error

    Parks Medical Electronics is recalling 349 vascular blood flow machines after two incidents where an air supply tube was connected to a patient's IV instead of a blood pressure cuff.

    Product
    Devices includes a Multi Port Inflator or without Multi Port Inflator (MPI). All the devices are vascular blood flow machines. Devices are distributed with pressure cuffs of varying sizes as accessories. Affected models include *2100-SX, 3000 series, 2017, 2016, 2015…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0729-2013·2012-12-05

    Mercer's Ice Cream Recalled for Undeclared Soy Lecithin

    Quality Dairy Farms Inc. is recalling Mercer's Ice Cream Cream N' Coffee Fudge because the product contains soy lecithin, which was not explicitly listed on the ingredient statement.

    Product
    Mercer's Ice Cream Cream N' Coffee Fudge, Half Gallon, (1.89 Liter), UPC 074513 003513
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0727-2013·2012-12-05

    Mercer's Ice Cream Recalled for Undeclared Soy Allergen

    Quality Dairy Farms Inc. is recalling Mercer's Ice Cream Old Fashioned Cookie Dough because the product contains soy lecithin, which was not explicitly listed on the ingredient statement.

    Product
    Mercer's Ice Cream Old Fashioned Cookie Dough, Half Gallon, (1.89 Liter), UPC 036667 200231
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0440-2013·2012-12-05

    Cooper Surgical Recalls Advincula Arch Uterine Manipulator Handles

    Cooper Surgical is recalling Advincula Arch handles because the internal steel rod may protrude through the shaft, posing a risk of injury during surgery.

    Product
    Cooper Surgical Advincula Arch , Reusable Uterine Manipulator Handle Ref: UMH750 The intended use of the RUMI Arch is in an operative endoscopy (laparoscopy) where a uterus is present and where positioning of the uterus, fallopian tubes and ovaries is desirable. These types…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0437-2013·2012-12-05

    Zimmer Recalls NexGen Knee Components Due to Manufacturing Cleaning Defects

    Zimmer is recalling specific lots of NexGen knee components because they were processed outside validated cleaning parameters, potentially leaving residual particulate.

    Product
    NexGen CompleteKnee Solution Stemmed Nonaugmentable Tibial component The NexGen¿¿ system is a semiconstrained, nonlinked condylar knee prostheses. The device is indicated for patients with severe knee pain and disability due to rheumatoid arthritis; osteoarthritis; traumatic…
    Category
    Medical Device
    Distribution
    13 states
  • HighNHTSA·12V561000·2012-12-04

    Lamborghini Recalls 2012 Aventador Vehicles for Headlight Aiming Defect

    Lamborghini is recalling 144 model year 2012 Aventador vehicles because the headlights may not aim vertically, potentially reducing visibility and blinding oncoming traffic.

    Product
    LAMBORGHINI — LAMBORGHINI AVENTADOR
    Category
    Vehicle
    Distribution
    Distributed nationwide