The Recall Desk

Hazard

Injury recalls

1,366 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
1,366
Critical
6
Severe
415
Most recent
2026-09-03

Of the 1,366 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 415 (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.

726–750 of 1366

  • HighFDA (Devices)·Z-1473-2017·2017-03-22

    Medtronic SharkCore Fine Needle Biopsy System Recalled for Handle Breakage

    Medtronic is recalling SharkCore Fine Needle Biopsy Systems because the handle may break during use, posing a risk of injury to patients or providers.

    Product
    SharkCore Fine Needle Biopsy System (22 GA); Material/Part #s: DSC-22-01
    Category
    Medical Device
    Distribution
    40 states
  • SevereNHTSA·17V178000·2017-03-14

    Mercedes-Benz Recalls 2016 G550 and G63 Due to Door Cable Defect

    Mercedes-Benz is recalling 2016 G550 and G63 vehicles because a door cable may break, preventing occupants from opening the door from inside after a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ G550, G63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17098·2017-02-28

    S.R. Smith Recalls Helix Pool Slides Due to Fall Hazard

    S.R. Smith is recalling Helix pool slides because children can fall off the side before reaching the pool, posing a risk of serious injury.

    Product
    Helix pool slides
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V123000·2017-02-27

    Ford Recalls 2016-2017 Edge, MKX, Continental for Air Bag Defect

    Ford is recalling 2016-2017 Edge, MKX, and Continental vehicles because the driver's air bag may not fully inflate or detach during a crash.

    Product
    LINCOLN — LINCOLN, FORD MKX, CONTINENTAL, EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V107000·2017-02-17

    Altec Recalls 2016 Digger Derrick Vehicles Due to Fastener Failure Risk

    Altec Industries is recalling 2016 DLB Digger Derrick vehicles because fasteners securing the outer rotation bearings may fail, potentially causing the boom to move unintentionally.

    Product
    ALTEC — ALTEC DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17084·2017-02-09

    Feld Entertainment Recalls Light-Spinner Toy Wands Due to Injury Hazard

    Feld Entertainment is recalling light-spinner toy wands sold at Disney shows because a top component can detach, exposing a metal rod that poses an injury risk to young children.

    Product
    Light-spinner toy wands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V076000·2017-02-08

    Mercedes-Benz Recalls 2017 E-Class Models Due to Air Bag Defect

    Mercedes-Benz is recalling 2017 E300 and E43 AMG vehicles because the front passenger air bag may fail to deploy due to an incorrectly installed sensor.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E300, AMG E43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V080000·2017-02-08

    Mercedes-Benz Recalls 2017 Models for Air Bag Ignition Failure

    Mercedes-Benz is recalling 2017 E300, E400, E550, GLA 250, and CLA250 vehicles because the pelvis or front passenger air bag inflator may fail to ignite in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E300, E400, GLA 250, CLA250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1064-2017·2017-02-01

    Villa Radiology Systems Recalls Apollo X-Ray Systems Due to Injury Risk

    Villa Radiology Systems LLC is recalling 66 Apollo multi-function x-ray systems after an injury incident involving inadvertent movement activation and delayed emergency stop response.

    Product
    Apollo: Models: 9784000131, 9784000231, 9784020131, 9784020231, 9784100231, 9784120131, 9784120231, 9784130131 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
    Category
    Medical Device
    Distribution
    26 states
  • SevereFDA (Devices)·Z-1063-2017·2017-02-01

    Villa Radiology Juno DRF X-ray Systems Recalled for Injury Risk

    Villa Radiology Systems LLC is recalling Juno DRF x-ray systems after an injury occurred due to a chain of faults involving physical barriers and labeling.

    Product
    Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
    Category
    Medical Device
    Distribution
    26 states
  • SevereFDA (Devices)·Z-1065-2017·2017-02-01

    Villa Radiology Systems Recalls Apollo DRF X-Ray Systems Due to Injury Risk

    Villa Radiology Systems LLC is recalling 66 Apollo DRF multi-function x-ray systems because a chain of faults led to an injury involving inadvertent movement activation.

    Product
    Apollo DRF: Model: 9784220831 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
    Category
    Medical Device
    Distribution
    26 states
  • SevereFDA (Devices)·Z-1066-2017·2017-02-01

    Villa Radiology Systems Recalls Apollo EZ X-Ray Systems Due to Injury Risk

    Villa Radiology Systems LLC is recalling 66 Apollo EZ multi-function x-ray systems because a chain of faults caused an injury to a user.

    Product
    Apollo EZ: Model: 9784152036 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
    Category
    Medical Device
    Distribution
    26 states
  • HighCPSC·17079·2017-01-31

    Teufelberger Recalls Static Ropes and Throwlines Due to Fall Hazards

    Teufelberger is recalling specific static ropes and throwlines because they are mislabeled as certified to NFPA safety standards, posing fall and injury risks to users.

    Product
    Static ropes and throwlines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17726·2017-01-12

    BRP Recalls Side-by-Side Off-Road Vehicles Due to Roll-Away Hazard

    BRP is recalling about 780 Can-Am Defender side-by-side off-road vehicles because they can unexpectedly roll away while in park, posing an injury risk.

    Product
    Side-by-side off-road vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V943000·2016-12-29

    Jaguar Recalls 2016-2017 XJ Models Due to Air Bag Defect

    Jaguar is recalling 2016-2017 XJ vehicles because the front passenger air bag may fail to deploy in a crash. Dealers will replace the air bag free of charge.

    Product
    JAGUAR — JAGUAR XJ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0810-2017·2016-12-28

    Oscor Breezeway Sheath Recalled Due to Inner Liner Fragmentation

    Oscor, Inc. is recalling 255 Breezeway sheaths because a fragment of the inner liner detached during insertion, posing a risk of injury.

    Product
    OSCOR BREEZEWAY 10F S60.8CM D65.6CM FIRM TIP Catalog # AB1061FT Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighNHTSA·16V930000·2016-12-23

    KME Recalls Fire Trucks Due to Ladder Position Sensor Defect

    Kovatch Mobile Equipment Corp. is recalling certain KME fire trucks because water may leak into the ladder position sensor, increasing the risk of injury.

    Product
    KME — KME PREDATOR SS AERIAL, PREDATOR AERIAL, PREDATOR PANTHER AERIAL, PREDATOR TDA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16C008000·2016-12-19

    Baby Trend Recalls Booster Seats Due to Harness Rivet Failure Risk

    Baby Trend is recalling specific Hybrid LX booster seats because a center adjuster rivet may break if used with children over 40 lbs, increasing injury risk in a crash.

    Product
    CHILD SEAT:HARNESS:STRAP/WEBBING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E094000·2016-12-15

    Autoliv Recalls Seatbelt Pretensioners Due to Detachment Risk

    Autoliv is recalling specific seatbelt retractors because a subcomponent may detach after deployment, creating a projectile hazard inside the vehicle.

    Product
    SEAT BELTS:PRETENSIONER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide