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.

20776–20800 of 50413

  • HighNHTSA·21V220000·2021-03-30

    Dennis Eagle Elite and Proview Recalled for Incorrect ABS Warning Light

    Dennis Eagle is recalling 2017-2021 Elite and Proview vehicles because the ABS warning light may illuminate incorrectly when brake pads wear out, potentially causing driver confusion.

    Product
    DENNIS EAGLE — DENNIS EAGLE PROVIEW, ELITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E024000·2021-03-30

    Cummins Recalls Electric Drivetrain Parts Due to High Voltage Shock Risk

    Cummins is recalling Electric Drivetrain part number PD7000 because it cannot detect isolation faults, posing a high voltage shock risk to service personnel.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:SHOCK PROTECTION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V223000·2021-03-30

    2020-2021 Lincoln Aviator vehicles recalled for backup camera display failure

    Ford is recalling 2020-2021 Lincoln Aviator vehicles because the backup camera display may not show video feed, affecting rear visibility. Free software updates are available from Ford dealers.

    Product
    LINCOLN — LINCOLN AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V221000·2021-03-30

    2021 Alfa Romeo Stelvio Side Curtain Air Bag May Fail to Deploy

    2021 Alfa Romeo Stelvio vehicles may have improperly crimped clamps in the side curtain air bag assembly, which can fail to deploy in a crash, increasing injury risk. Chrysler will replace the assemblies at no cost.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V222000·2021-03-30

    Pierce Recalls 2016-2018 Trucks Due to Excessively Bright Rear LED Lights

    Pierce Manufacturing is recalling 2016-2018 Enforcer, Freightliner, and Saber trucks because rear LED lights may be too bright, potentially blinding other drivers.

    Product
    PIERCE — PIERCE ENFORCER, SABER, FREIGHTLINER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E023000·2021-03-30

    Nado LED Headlight Bulb Recall for Excessive Glare and Brightness

    Nado Stuff is recalling MICTUNING LED headlight bulbs that create excessive glare, increasing crash risk. Owners will receive a full refund.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21E022000·2021-03-30

    BEAMTECH LED Headlight Bulbs Recalled for Excessive Glare and Brightness

    Guangzhou Lengzhilu Trading Co., Ltd. is recalling specific BEAMTECH LED headlight bulbs because they create excessive glare, failing federal safety standards.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V218000·2021-03-29

    Winnebago Recalls 2020 Minnie RVs Due to Incorrect Tire Labeling

    Winnebago is recalling 2020 Minnie vehicles because the Tire and Loading Information label lists the wrong tire size, which could lead to improper tire installation and increased crash risk.

    Product
    WINNEBAGO — WINNEBAGO MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V219000·2021-03-29

    2021 Forest River Berkshire Class A Motorhomes: Brake Light Reflection Defect

    Forest River is recalling certain 2021 Berkshire Class A motorhomes due to brake lights that may not adequately reflect light. The defect affects visibility and compliance with Federal Motor Vehicle Safety Standards.

    Product
    FOREST RIVER — FOREST RIVER BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V216000·2021-03-26

    2020 Mercedes-Benz E-Class passenger seat limiter safety recall

    Mercedes-Benz is recalling certain 2020-2021 E-Class and AMG models due to a passenger seat limiter defect that may allow the seat to position too close to the frontal airbag, increasing injury risk during airbag deployment.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG E63S, E63 AMG, E 350, AMG E53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V211000·2021-03-25

    Chevrolet Camaro 2017-2021 Air Bag Emblem Separation Recall

    General Motors is recalling certain 2017-2021 Chevrolet Camaro vehicles because the plastic 'Camaro' emblem on the steering wheel air bag cover may separate during air bag deployment, creating a projectile hazard.

    Product
    CHEVROLET — CHEVROLET CAMARO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21733·2021-03-25

    KTM, Husqvarna, and GASGAS Recall Competition Motorcycles Due to Crash Hazard

    KTM, Husqvarna, and GASGAS are recalling about 1,470 model year 2021 closed course competition motorcycles because the drive chain can break, posing a crash hazard.

    Product
    KTM, Husqvarna and GASGAS closed course competition motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V212000·2021-03-25

    2021 Ducati Multistrada engine valve defect increases crash risk

    Certain 2021 Ducati Multistrada V4 S motorcycles may have excessive valve guide wear that could break the valve head, decreasing engine performance and increasing crash risk. Ducati will replace the affected motorcycle engines at no cost.

    Product
    DUCATI — DUCATI MULTISTRADA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1269-2021·2021-03-24

    Canon Catheterization Table Recall Due to Potential Tilt Hazard

    Canon is recalling 145 INTERVENTIONAL ANGIOGRAPHY SYSTEMS because table fastening bolts may loosen, causing the table to tilt.

    Product
    Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000V Catheterization Table CAT-880B Canon CATHETERIZATION TABLE, MODEL CAT-880B INPUT 220V - Product Usage: indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1274-2021·2021-03-24

    Siemens HSV-2 Test Kits Recalled for Potential False Positive Results

    Siemens is recalling ADVIA Centaur4P Herpes-2 IgG test kits due to stability and calibration failures that may cause false positive results.

    Product
    Enzyme linked immunosorbent assay, for herpes simplex virus, hsv-2
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-1273-2021·2021-03-24

    Philips CT Systems Recalled for Potential Couch Movement Failure

    Philips is recalling 109 CT systems because a defect in the Incisive CT couch actuators could cause the couch to fail to self-lock and move downward unexpectedly.

    Product
    Philips CT systems are advanced continuous-rotation computed tomography systems suitable for a wide range of computed tomographic (CT) applications - Product Usage: intended for use in the head and whole body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1276-2021·2021-03-24

    Epimed Feth-R-Kath Catheter Recalled for Coating Deterioration

    Epimed International is recalling Feth-R-Kath Catheters because the outer coating may crack or flake off. The recall covers 5,835 units distributed nationwide.

    Product
    Feth-R-Kath Catheter, 19g x 24". Intended Use:Radlo Opaque Epidural Catheter Catalog #: 157-1924 Intended for epidural anesthesia and is limited to placement of 72 hours or less
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1253-2021·2021-03-24

    Siemens SOMATOM CT Software Recall for Workflow Interruptions

    Siemens is recalling specific software versions for SOMATOM CT systems due to sporadic errors that may interrupt scanning workflows and delay diagnosis.

    Product
    Software versions syngo.CT VA30A_SP2 or syngo.CT VA30A_SP2a in the Computed tomography systems as follows: SOMATOM go.Now (Model 11061610)SOMATOM go.Up (Models 11061620 & 11061628) SOMATOM go.All (Model 11061630) SOMATOM go.Top (Models 11061640 & 11061648) SOMATOM go.Sim…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1265-2021·2021-03-24

    Philips Incisive CT System Recalled for Gantry Actuator Failure Risk

    Philips is recalling 105 Incisive CT Computed Tomography X-ray Systems because gantry actuators may fail, causing the gantry to tilt forward.

    Product
    Incisive CT Computed Tomography X-ray System Model: 728143
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1254-2021·2021-03-24

    Mindray BeneVision Distributed Monitoring System Recalled for Intermittent Freezes

    Mindray is recalling 1,938 BeneVision Distributed Monitoring Systems because they may intermittently freeze, causing telemetry data to stop communicating to the central system.

    Product
    Mindray BeneVision Distributed Monitoring System( DMS) 1. p/n 115-051209-00 2. p/n 115-034414-00 and 115-034413-00 when used with the following software versions: 03.04.00 04.01.00 04.03.00 04.04.00 04.04.01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1272-2021·2021-03-24

    Accuray CyberKnife Treatment Delivery System Recalled for Loose Set Screws

    Accuray is recalling 243 CyberKnife Treatment Delivery Systems because set screws can loosen, allowing the treatment couch to roll unexpectedly.

    Product
    CyberKnife Treatment Delivery System - Product Usage: indicated for image-guided stereotactic radiosurgery and precision radiotherapy for lesions, tumors and conditions anywhere in the body when radiation treatment is indicated.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V208000·2021-03-24

    2021 Genesis GV80 High-Pressure Fuel Tube Recall: Fire Risk

    Hyundai is recalling certain 2021 Genesis GV80 and G80 vehicles with 2.5-liter turbo engines due to a high-pressure fuel tube that may not seal properly, potentially allowing fuel to leak and increase fire risk.

    Product
    GENESIS — GENESIS GV80, G80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0340-2021·2021-03-24

    Giant Eagle Recalls Market District Pretzels Due to Undeclared Pecans

    Giant Eagle is recalling Market District Gourmet Pretzels because they contain undeclared pecans, a major food allergen.

    Product
    Market District Gourmet Pretzel Gift Bag PLU 45505 Net Wt 9 oz Market District Gourmet Pretzel Platter PLU 25206 Net Wt 48 oz
    Category
    Food
    Distribution
    2 states