The Recall Desk

Hazard

Injury recalls

1,375 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
1,375
Critical
6
Severe
418
Most recent
2026-10-21

Of the 1,375 injury recalls we have scored against our rubric, 6 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 418 (30%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all injury recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

526–550 of 1375

  • SevereNHTSA·18V781000·2018-11-06

    Lotus Recalls 2018 Evora Vehicles for Steering Column Assembly Error

    Lotus is recalling 2018 Evora vehicles because an assembly error may prevent the steering column from collapsing properly in a frontal collision, increasing injury risk.

    Product
    LOTUS — LOTUS EVORA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V775000·2018-11-01

    Ford Recalls 2010-2012 Vehicles for Passenger Air Bag Defect

    Ford is recalling specific 2010-2012 vehicles to replace passenger air bag modules that may fail to inflate properly in a crash.

    Product
    LINCOLN — LINCOLN, MERCURY, FORD MKZ, MILAN, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19027·2018-11-01

    Black & Decker Recalls Hammer Drills Due to Side Handle Injury Hazard

    Black & Decker is recalling specific hammer drills and drill drivers because the side handles can slip or break, posing an injury risk.

    Product
    Black & Decker, Bostitch and Porter-Cable Hammer Drills and Drill Drivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·107-2018·2018-10-31

    Procesadora La Hacienda Recalls Corned Beef Due to Foreign Matter

    Procesadora La Hacienda, Inc. is recalling ready-to-eat corned beef products that may contain soft plastic or metal. The products were distributed to institutions in Puerto Rico.

    Product
    Procesadora La Hacienda, Inc. — Procesadora La Hacienda, Inc., Recalls Beef Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·18V757000·2018-10-26

    Altec Recalls 2018 Digger Derricks and Aerial Devices for Fastener Failure

    Altec is recalling 2018 Digger Derricks and Aerial Devices because high-strength fasteners may fail, causing the pedestal to separate from the turn table and increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE, DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V727000·2018-10-18

    Charles Machine Recalls 2018 Ditch Witch Trailers Due to Jib Boom Defect

    Charles Machine is recalling 2018 Ditch Witch trailers with vacuum excavators because the jib boom can become loose and swing outside the trailer while being towed.

    Product
    CHARLES MACHINE — CHARLES MACHINE DITCH WITCH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3265-2018·2018-10-03

    Bausch + Lomb Stellaris Elite Vit Cutter Back Cap Separation Recall

    Bausch & Lomb is recalling Stellaris Elite 20 GA Vit Cutters because the back cap may separate from the body of the device.

    Product
    Bausch + Lomb Stellaris Elite 20 GA Vit Cutter, Model BL5626, 7500 cpm, packaged in sterile pouches, 6/shipper.
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-3221-2018·2018-10-03

    Philips Allura Xper FD2O Ceiling Monitor Suspension Recall

    Philips is recalling 5,115 Allura Xper FD2O systems because the ceiling monitor suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.

    Product
    Allura Xper FD2O, System Code 722006 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3229-2018·2018-10-03

    Philips FlexVision Monitor Ceiling Suspension Recall for Detachment Risk

    Philips is recalling FlexVision Monitor Ceiling Suspensions because the monitor may detach from the actuator rotor shaft, posing a risk of injury to patients, users, and bystanders.

    Product
    AIIuraXperFDlO, System Code 722010 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3248-2018·2018-10-03

    Swissray Medical Recalls ddR Formula B X-ray Systems for Movement and Calibration Issues

    Swissray Medical is recalling 26 ddR Formula B X-ray systems in the U.S. due to potential arm movement, calibration loss, and communication loss that could cause injury.

    Product
    ddR Formula B X-ray System, ddR Formula B Product Usage: X-ray system used for imaging
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3213-2018·2018-10-03

    Philips INTEGRIS Allura 9 Monitor Ceiling Suspension Recall

    Philips is recalling INTEGRIS Allura 9 systems because the monitor ceiling suspension may detach, causing the monitor to fall and risk injury.

    Product
    INTEGRIS Allura 9, System Code 722018 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3231-2018·2018-10-03

    Philips AIIura Xper F010 DR Table Recall for Monitor Detachment Risk

    Philips is recalling AIIura Xper F010 DR Tables because the ceiling monitor suspension may detach, posing a risk of injury to patients and staff.

    Product
    AIIura Xper F010 DR Table, System Code 722022 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3225-2018·2018-10-03

    Philips Allura Xper FD1O C Ceiling Monitor Recall for Detachment Risk

    Philips is recalling 5,115 Allura Xper FD1O C systems because the ceiling monitor suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.

    Product
    Allura Xper FD1O C, System Code 722001 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3238-2018·2018-10-03

    Philips Medical Monitor Ceiling Suspension Recall for Detachment Risk

    Philips is recalling 5,115 medical monitor ceiling suspensions because the monitor may detach from the actuator, posing a risk of injury to patients and users.

    Product
    Cesar-DMCP-Visub(HM2000/3000), System Code 72239 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3236-2018·2018-10-03

    Philips Allura Xper F020 Biplane DR Table Recall for Monitor Suspension Defect

    Philips is recalling 5,115 Allura Xper F020 Biplane DR Tables because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.

    Product
    Allura Xper F020 Biplane DR Table, System Code 722020 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3217-2018·2018-10-03

    Philips INTEGRIS Allura 15-12 Biplane Monitor Suspension Recall

    Philips is recalling INTEGRIS Allura 15-12 biplane systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.

    Product
    INTEGRIS Allura 15-12 (biplane), System Code 722044 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3239-2018·2018-10-03

    Philips Medical Monitor Ceiling Suspension Recall Due to Detachment Risk

    Philips is recalling 5,115 medical monitor ceiling suspensions because the monitor may detach and fall, posing an injury risk to patients and users.

    Product
    Cesar Powerpack-Visub(V3000), System Code 72243 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3234-2018·2018-10-03

    Philips Allura Xper F020 DR Table Recall for Monitor Suspension Defect

    Philips is recalling 5,115 Allura Xper F020 DR Tables because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.

    Product
    Allura Xper F020 DR Table, System Code 722015 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·19003·2018-10-03

    Walmart Recalls Ozark Trail Camp Axes Due to Injury Hazard

    Walmart is recalling Ozark Trail camp axes because the axe head can detach from the handle, posing an injury hazard.

    Product
    Ozark Trail camp axes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V691000·2018-10-03

    Spartan Emergency Vehicles Recalled for Loose EMS Cabinet Fasteners

    Spartan Motors is recalling 2001-2019 MetroStar and Gladiator emergency vehicles because EMS cabinet fasteners may be the wrong size, posing a crash injury risk.

    Product
    SPARTAN — SPARTAN METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3224-2018·2018-10-03

    Philips Allura Xper FD2O Biplane Recall for Monitor Suspension Detachment Risk

    Philips is recalling 5,115 Allura Xper FD2O Biplane systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.

    Product
    Allura Xper FD2O Biplane, System Code 722008 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3216-2018·2018-10-03

    Philips INTEGRIS Allura Monitor Ceiling Suspension Recall for Detachment Risk

    Philips is recalling INTEGRIS Allura 15-12 systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.

    Product
    INTEGRIS Allura 15-12 (mono), System Code 722043 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·18767·2018-09-20

    Titan Recalls Weight Lifting Safety Straps Due to Injury Hazard

    Titan is recalling weight lifting safety straps because stitching can come loose, causing heavy weights to fall. No injuries have been reported.

    Product
    Titan safety straps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V623000·2018-09-13

    Forest River Berkshire Motorhomes Recalled for Door Latch Defect

    Forest River is recalling 2019 Berkshire motorhomes because improperly adjusted door latch rods may allow the entry door to open while the vehicle is moving.

    Product
    FOREST RIVER — FOREST RIVER BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide