The Recall Desk

Hazard

Serious Injury recalls

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

What the numbers show

Total
345
Critical
77
Severe
237
Most recent
2026-08-06

Of the 345 serious injury recalls we have scored against our rubric, 77 (22%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 237 (69%) 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 serious 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.

276–300 of 345

  • SevereNHTSA·15E041000·2015-05-18

    Takata Passenger Air Bag Inflator Recall for 2001-2008 Vehicles

    Takata is recalling specific passenger frontal air bag inflators for 2001-2008 vehicles due to a risk of rupture during deployment.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V287000·2015-05-15

    Nissan Recalls Vehicles Due to Passenger Air Bag Inflator Rupture Risk

    Nissan is recalling specific 2001-2006 models because the passenger air bag inflator may rupture during deployment, potentially sending metal fragments into the vehicle.

    Product
    NISSAN — NISSAN, INFINITI PATHFINDER, FX35, I30, FX45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V286000·2015-05-13

    Toyota Recalls Vehicles for Front Passenger Air Bag Inflator Rupture Risk

    Toyota is recalling specific 2002-2007 Lexus, Toyota, and Pontiac vehicles because the front passenger air bag inflator may rupture during a crash, potentially causing serious injury or death.

    Product
    PONTIAC — PONTIAC, LEXUS, TOYOTA VIBE, SC, SEQUOIA, TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V284000·2015-05-13

    Toyota Recalls 2004-2005 RAV4 Vehicles Due to Air Bag Defect

    Toyota is recalling 2004-2005 RAV4 vehicles because the driver's air bag inflator may rupture during deployment, posing a risk of serious injury or death.

    Product
    TOYOTA — TOYOTA RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V285000·2015-05-13

    Toyota Recalls Vehicles for Defective Passenger Air Bag Inflators

    Toyota is recalling approximately 1.97 million vehicles, including Pontiac, Lexus, and Toyota models, to replace passenger air bag inflators that may rupture.

    Product
    PONTIAC — PONTIAC, LEXUS, TOYOTA VIBE, SC, SEQUOIA, TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V226000·2015-04-17

    Nissan Recalls Infiniti Vehicles for Air Bag Inflator Rupture Risk

    Nissan is recalling specific Infiniti models because the passenger air bag inflator may rupture during deployment, potentially causing serious injury or death.

    Product
    INFINITI — INFINITI FX35, FX45, I35, M35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V787000·2014-12-12

    Ford Recalls 2005-2006 GT Vehicles for Air Bag Inflator Defect

    Ford is recalling 2005-2006 GT vehicles sold in high-humidity areas because the passenger air bag inflator may rupture during deployment, potentially causing serious injury.

    Product
    FORD — FORD GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0456-2015·2014-12-10

    ConMed Adult Radiotransparent Electrodes Recalled for Connection Design Changes

    ConMed is recalling 174,610 Adult Radiotransparent Electrodes because design changes to Philips AED connections may cause therapy delays, risking patient death or serious injury.

    Product
    ADULT Radiotransparent Electrode, REF/Catalog Number 2001H-PC, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0461-2015·2014-12-10

    ConMed Pediatric Multifunction Electrodes Recalled for Connection Design Flaws

    ConMed is recalling Pediatric R2 Multifunction Electrodes because design changes to the connection with Philips Heartstart devices may cause connection failures, potentially delaying therapy and leading to patient death or serious injury.

    Product
    CONMED PEDIATRIC R2 Multifunction Electrodes, REF/Catalog Number 3115-1750, Direct Connect to Philips Heartstart, Rx ONLY --- ASSEMBLED IN MEXICO -Intended for use during defibrillation, cardioversion, pacing, and ECG monitoring applications. This product is a single-use, disposa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0455-2015·2014-12-10

    ConMed Adult Radiotransparent Electrode Recall Due to Connection Design Changes

    ConMed is recalling Adult Radiotransparent Electrodes because design changes to Philips AED connections may cause connection failures, potentially delaying therapy and resulting in patient death or serious injury.

    Product
    ADULT Radiotransparent Electrode, REF/Catalog Number 2001H-C, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0458-2015·2014-12-10

    ConMed Adult Radiotransparent Electrode Recall Due to Connection Failure Risk

    ConMed is recalling Adult Radiotransparent Electrodes because design changes to Philips AEDs may prevent connection, delaying therapy and risking patient death or serious injury.

    Product
    ADULT Radiotransparent Electrode, REF/Catalog Number 2516H-PC, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0460-2015·2014-12-10

    ConMed Pediatric Electrodes Recalled Due to Connection Design Changes

    ConMed is recalling 174,610 pediatric electrodes because design changes to Philips AEDs may prevent connection, delaying therapy and risking death or serious injury.

    Product
    MINI PEDIATRIC Radiotransparent Electrode, REF/Catalog Number 2602H, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR--Intended for use during defibrillation, cardioversion, pacing, and ECG monitoring applications. This product is a single-use,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0459-2015·2014-12-10

    ConMed Pediatric Radiotransparent Electrode Recall Due to Connection Design Changes

    ConMed is recalling 174,610 pediatric radiotransparent electrodes because design changes to Philips AED connections may cause therapy delays, risking patient death or serious injury.

    Product
    PEDIATRIC Radiotransparent Electrode, REF/Catalog Number 2603H, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0454-2015·2014-12-10

    ConMed Adult Radiotransparent Electrodes Recalled for Connection Design Failure

    ConMed is recalling Adult Radiotransparent Electrodes because a design change in Philips AEDs may prevent connection, delaying therapy and risking patient death or serious injury.

    Product
    ADULT Radiotransparent Electrode, REF/Catalog Number 2001H, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR Intended for use during defibrillation, cardioversion, pacing, and ECG monitoring applications. This product is a single-use, disposab
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0457-2015·2014-12-10

    ConMed Adult Radiotransparent Electrode Recall Due to Connection Design Changes

    ConMed is recalling 174,610 Adult Radiotransparent Electrodes because design changes to Philips AED connections may cause therapy delays, risking patient death or serious injury.

    Product
    ADULT Radiotransparent Electrode, REF/Catalog Number 2516H, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0462-2015·2014-12-10

    ConMed Multifunction Electrodes Recalled for Connection Design Failure

    ConMed is recalling multifunction electrodes due to a design change that may prevent connection to Philips AEDs, potentially delaying therapy.

    Product
    CONMED ADULT R2 Multifunction Electrodes, REF/Catalog Number 3115-1751, Direct Connect to Philips Heartstart, Rx ONLY --- ASSEMBLED IN MEXICO -Intended for use during defibrillation, cardioversion, pacing, and ECG monitoring applications. This product is a single-use, disposable
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V770000·2014-12-03

    Chrysler Recalls 2004-2005 Vehicles Due to Air Bag Inflator Rupture Risk

    Chrysler is recalling 2004-2005 Dodge and Chrysler vehicles sold in high-humidity areas because the passenger air bag inflator may rupture during deployment.

    Product
    DODGE — DODGE, CHRYSLER RAM 3500, RAM 2500, MAGNUM, DURANGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V763000·2014-12-01

    Subaru Recalls 2003-2005 Models for Air Bag Inflator Rupture Risk

    Subaru is recalling 2003-2005 Legacy, Outback, and Baja vehicles in high-humidity areas because the passenger air bag inflator may rupture during deployment.

    Product
    SUBARU — SUBARU OUTBACK, LEGACY, BAJA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E073000·2014-11-13

    Takata Frontal Air Bag Inflators Recalled for Rupture Risk

    Takata is recalling certain passenger frontal air bag inflators that may rupture during deployment, potentially causing serious injury or death.

    Product
    AIR BAGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V700000·2014-11-04

    Honda Recalls Multiple Models for Air Bag Inflator Rupture Risk

    Honda is recalling specific 2001-2006 models sold in high-humidity areas because the passenger air bag inflator may rupture during deployment.

    Product
    HONDA — HONDA, ACURA CIVIC HYBRID, PILOT, RIDGELINE, RL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V668000·2014-10-24

    Nissan Recalls Infiniti QX56 and QX80 for Air Bag Defect

    Nissan is recalling 2013 Infiniti QX56 and 2014 QX80 vehicles because the driver's air bag inflator may contain an incorrect part that could rupture during deployment.

    Product
    INFINITI — INFINITI QX80, QX56
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V372000·2014-06-26

    GM Recalls 2013-2014 Chevrolet Cruze for Driver Air Bag Defect

    General Motors is recalling 2013-2014 Chevrolet Cruze vehicles because the driver's air bag inflator may rupture in a crash, potentially causing serious injury.

    Product
    CHEVROLET — CHEVROLET CRUZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V353000·2014-06-20

    Honda and Acura Vehicles Recalled for Takata Air Bag Inflator Defect

    Honda is recalling specific 2003-2006 vehicles sold or registered in California due to a Takata air bag inflator defect that could rupture during deployment.

    Product
    HONDA — HONDA, ACURA RIDGELINE, PILOT, RL, ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1638-2014·2014-05-28

    Siemens MAMMOMAT Inspiration PC Monitor Holder Recall for Injury Risk

    Siemens is recalling five MAMMOMAT Inspiration mammography units because the PC monitor holder can break, causing the monitor to fall and potentially injure users.

    Product
    MAMMOMAT Inspiration. Intended for mammography exams, screening, diagnosis, and stereotactic biopsies under the supervision of medical professionals.
    Category
    Medical Device
    Distribution
    5 states
  • SevereFDA (Devices)·Z-1460-2014·2014-04-23

    Siemens AXIOM Vertix MD Trauma Systems Recalled for U-Arm Drop Risk

    Siemens is recalling two AXIOM Vertix MD Trauma systems because defective steel ropes may cause the U-arm to drop unexpectedly, posing a risk of serious injury to patients.

    Product
    AXIOM Vertix MD Trauma systems radiographic X-ray
    Category
    Medical Device
    Distribution
    2 states