The Recall Desk

Hazard

Death recalls

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

What the numbers show

Total
281
Critical
111
Severe
152
Most recent
2026-08-20

Of the 281 death recalls we have scored against our rubric, 111 (40%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 152 (54%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all death 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.

101–125 of 281

  • SevereNHTSA·18V717000·2018-10-12

    Mazda Recalls CX-7, CX-9, and Mazda6 for Air Bag Inflator Defect

    Mazda is recalling 2010-2015 CX-7, CX-9, and Mazda6 vehicles because the front passenger air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    MAZDA — MAZDA CX-7, CX-9, MAZDA6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18V662000·2018-09-27

    Honda Recalls 2010-2014 Vehicles for Air Bag Inflator Explosion Risk

    Honda is recalling 2010-2014 Ridgeline, Element, and Acura RL vehicles because the passenger air bag inflator may explode, posing a risk of serious injury or death.

    Product
    ACURA — ACURA, HONDA RL, RIDGELINE, ELEMENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V661000·2018-09-27

    Honda Recalls Vehicles for Frontal Air Bag Inflator Explosion Risk

    Honda is recalling specific 2010-2015 models because the passenger frontal air bag inflator may explode, potentially causing serious injury or death.

    Product
    HONDA — HONDA, ACURA ACCORD, PILOT, TSX, CROSSTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·081-2018·2018-09-19

    Cargill Recalls Ground Beef Due to E. coli O26 Contamination

    Cargill Meat Solutions is recalling approximately 132,606 pounds of ground beef products that may be contaminated with E. coli O26. The recall follows an investigation linking the bacteria to 17 illnesses and one death.

    Product
    Cargill Meat Solutions — Cargill Meat Solutions Recalls Ground Beef Products due to Possible E. coli O26 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18V452000·2018-07-06

    Nissan Recalls 2007-2008 Versa Models Due to Air Bag Inflator Defect

    Nissan is recalling 2007-2008 Versa sedans and hatchbacks because the passenger air bag inflators may explode. This defect could cause metal fragments to strike occupants, resulting in serious injury or death.

    Product
    NISSAN — NISSAN VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2252-2018·2018-06-27

    Draeger Fabius GS MRI Anesthesia Machine Recalled for Hypoxia Risk

    Draeger Medical is recalling four Fabius GS MRI Anesthesia Machines because a fault could allow the device to deliver a hypoxic gas mixture to patients, potentially causing death.

    Product
    Fabius GS MRI Anesthesia Machine; Cat. no. 8607300 Product Usage: Inhalation anesthesia machines for use in operating, induction and recovery rooms. They may be used with O2, N2O, and AIR supplied by a medical gas pipeline system or by externally mounted gas cylinders. Fabius
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2251-2018·2018-06-27

    Draeger Fabius GS Tiro Anesthesia Machine Recalled for Hypoxia Risk

    Draeger Medical is recalling 31 Fabius GS Tiro anesthesia machines because a fault could allow 100% nitrous oxide delivery, creating a risk of hypoxic mixtures and patient death.

    Product
    Fabius GS Tiro Anesthesia Machine; Cat. no. 8606000 Product Usage: Inhalation anesthesia machines for use in operating, induction and recovery rooms. They may be used with O2, N2O, and AIR supplied by a medical gas pipeline system or by externally mounted gas cylinders. Fabiu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2254-2018·2018-06-27

    Draeger Perseus A500 Anesthesia Machine Recalled for Hypoxic Mixture Risk

    Draeger Medical is recalling 33 Perseus A500 anesthesia machines because a fault could allow the device to deliver a hypoxic gas mixture to patients.

    Product
    Perseus A500 Anesthesia Machine; Cat. no. MK06000 Product V Product Usage: Intended for use in anesthetizing adults, children, and neonates and can be used for automatic and manual ventilation, pressuresupported spontaneous breathing, and spontaneous breathing. Perseus is
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V427000·2018-06-22

    Audi Recalls A4, A6, and RS4 Models Due to Air Bag Inflator Defect

    Volkswagen Group of America is recalling specific Audi models because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    AUDI — AUDI A4, A6, RS 4, RS4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2227-2018·2018-06-20

    Seaberg SAM XT-C Tourniquet Recall Due to Potential Buckle Failure

    The Seaberg Company is recalling SAM XT-C tourniquets because internal testing showed stitches securing the buckle might fail, posing a risk of serious injury or death.

    Product
    Part #: SAM XT-C, Model: Hi-Viz Orange or Civilian
    Category
    Medical Device
    Distribution
    23 states
  • SevereFDA (Devices)·Z-2228-2018·2018-06-20

    Seaberg SAM XT-C Tourniquet Recalled for Potential Buckle Stitch Failure

    The Seaberg Company is recalling SAM XT-C tourniquets because internal testing showed stitches securing the buckle could fail, posing a risk of serious injury or death.

    Product
    Part #: SAM XT-C, Model: Hi-Viz Blue
    Category
    Medical Device
    Distribution
    23 states
  • SevereFDA (Devices)·Z-2226-2018·2018-06-20

    Seaberg SAM XT-M Tourniquet Recalled for Potential Buckle Failure

    The Seaberg Company is recalling SAM XT-M tourniquets because internal testing found stitches securing the buckle could fail, posing a risk of serious injury or death.

    Product
    Part #: SAM XT-M, Model: Tactical Black or Military
    Category
    Medical Device
    Distribution
    23 states
  • CriticalNHTSA·18V402000·2018-06-15

    Mazda Recalls Vehicles Due to Passenger Air Bag Inflator Explosion Risk

    Mazda is recalling specific 2003-2011 models because passenger air bag inflators may explode during deployment, potentially causing serious injury or death.

    Product
    MAZDA — MAZDA MAZDA6, MPV, RX-8, MAZDASPEED6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18V404000·2018-06-15

    Mazda Recalls MPV and RX-8 Vehicles for Air Bag Inflator Defect

    Mazda is recalling 2005-2006 MPV and 2005-2009 RX-8 vehicles because the passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    MAZDA — MAZDA MPV, RX-8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18V403000·2018-06-15

    Mazda Recalls 2009-2010 RX-8 Vehicles for Air Bag Inflator Defect

    Mazda is recalling 2009-2010 RX-8 vehicles because the passenger air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    MAZDA — MAZDA RX-8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1536-2018·2018-06-13

    FDA Recalls Ethanol Extraction 190 Proof Grain Alcohol Due to Methanol Contamination

    Lake Michigan Distilling is recalling 190 Proof Non-Denatured Grain Alcohol due to methanol contamination that could cause serious injury or death if consumed.

    Product
    Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol, Multiple sizes: 8 oz, 16 oz, 32 oz, 64 oz, 1 gal, 2.5 gals, 5 gals, 55 gallon drum, 8oz clear PVC cylinder bottles, all others heavy-duty polyethylene bottles (except single 55-gallon plastic drum).
    Category
    Food
    Distribution
    51 states
  • SevereNHTSA·18V406000·2018-06-13

    Volkswagen Recalls 2003 Models for Air Bag Inflator Defect

    Volkswagen is recalling 2003 EuroVan, Jetta, Passat, and Golf vehicles because the driver's air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    VOLKSWAGEN — VOLKSWAGEN EUROVAN, JETTA, PASSAT, GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V381000·2018-06-07

    Ferrari Recalls 2012 Models Due to Passenger Air Bag Inflator Defect

    Ferrari is recalling 2012 California, 458, and FF models because the passenger air bag inflator may explode in a crash, potentially causing serious injury or death.

    Product
    FERRARI — FERRARI CALIFORNIA, FF, 458
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1774-2018·2018-05-23

    Abbott HeartMate 3 LVAS Implant Kit Recalled for Graft Occlusion Risk

    Abbott is recalling HeartMate 3 LVAS Implant Kits due to reports of outflow graft twist occlusions that can cause serious adverse events.

    Product
    Thoratec HeartMate 3 LVAS Implant Kit, Rx Only, Catalog # 106524US, 106524, 10652INT - LVAS KIT, HM 3 Indicated for providing short-term hemodynamic support in patients with advanced refractory left ventricular heart failure.
    Category
    Medical Device
    Distribution
    35 states
  • SevereNHTSA·18V255000·2018-04-20

    Altec Recalls 1992-2006 Digger Derrick Trucks Due to Boom Pivot Pin Failure

    Altec Industries is recalling 1992-2006 Digger Derrick trucks because a specific boom pivot pin may fail, causing unexpected boom movement that increases the risk of injury or death.

    Product
    ALTEC — ALTEC DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V247000·2018-04-18

    Volkswagen Recalls 2006-2007 Passat Vehicles Due to Air Bag Inflator Defect

    Volkswagen is recalling 2006-2007 Passat sedans and wagons because the driver's air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    VOLKSWAGEN — VOLKSWAGEN PASSAT, PASSAT WAGON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1365-2018·2018-04-18

    Fresenius Liberty Select Cycler Recalled for Software Overfill Risk

    Fresenius Medical Care is recalling Liberty Select Cyclers due to a software issue that may cause overfill, posing a risk of serious injury or death.

    Product
    Liberty Select Cycler (SW v.2.8.7), Material Number RTLR108343 Product Usage: The device is indicated for acute and chronic peritoneal dialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V188000·2018-03-23

    Ferrari Recalls 458 Italia and California Models for Air Bag Defect

    Ferrari is recalling 2009-2011 California and 2010-2011 458 Italia vehicles because passenger air bag inflators may explode during a crash, posing a risk of serious injury or death.

    Product
    FERRARI — FERRARI 458 ITALIA, CALIFORNIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V138000·2018-02-27

    Altec Recalls 2004-2005 Aerial Devices Due to Boom Failure Risk

    Altec Industries is recalling 2004-2005 aerial devices and elevator vehicles because the fiberglass upper boom may degrade and fail, increasing the risk of injury or death.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide