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.

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 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.

1101–1125 of 1366

  • SevereFDA (Devices)·Z-2113-2012·2012-08-08

    Sunrise Medical Recalls Padded Swing Away Arm Rests Due to Injury Reports

    Sunrise Medical is recalling 14,035 Padded Swing Away Arm Rests for specific wheelchair models because reports indicate injury when the armrest is used to support full body weight.

    Product
    Padded Swing Away Arm Rest with Receiver; Uses on wheelchair models: Quickie Q7 (EIR4), GT (EIR3), GTi (EIT4) and Zippie Zone (EIRZ1). Product Usage: To empower physically challenged persons by providing a means of mobility. This includes temporary and permanent conditions.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·12V384000·2012-08-03

    Glaval Transit Bus Recall for Roof Hatch Opening Force Defect

    Glaval Bus is recalling 2011-2012 models because roof escape hatches may require excessive force to open, potentially hindering emergency exits.

    Product
    GLAVAL BUS — GLAVAL BUS, GLAVAL ENTOURAGE, PRIMETIME, SPORT, UNIVERSAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2077-2012·2012-08-01

    Anspach Effort Recalls Sterile Bone Cutting Burrs Due to Breakage Risk

    The Anspach Effort, Inc. is recalling specific sterile bone cutting burrs because the cutter may come apart during use.

    Product
    .***ANSPACH***Sterile. REF SHD-4820DS***QTY: 1, 4.8 mm x 2mm Twist Drill with Depth Stop. Use with SHORT-HD Attachment ***RX Only Product Usage: Cutting and shaping bone including bones of the spine and cranium.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·12V362000·2012-07-25

    Micro Bird Recalls G5 School Buses for Roof Hatch Friction Issues

    Micro Bird is recalling 2011-2012 G5 school buses because roof escape hatches may be too hard to open, potentially hindering emergency egress.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V352000·2012-07-24

    Hyundai Recalls 2012-2013 Sonata Vehicles Due to Airbag Defect

    Hyundai is recalling 2012-2013 Sonata vehicles because the curtain side airbags may inflate without a deployment command, increasing the risk of injury and driver distraction.

    Product
    HYUNDAI — HYUNDAI SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1949-2012·2012-07-18

    Arjo Sara Plus Patient Lifter Recalled for Exposed Metal Bracket Injury Risk

    ArjoHuntleigh is recalling Sara Plus Mobile Patient Lifters because removing the knee pad assembly exposes a metal support bracket, posing an injury risk.

    Product
    Sara Plus Mobile Patient Lifter; manufactured for Arjo by Medibo Medical Products N.V., Heikant 5, B-3930 Hamont-Achel, Belgium; Models HEP0001-US and HEP1001-US. The Sara Plus is a standing and raising aid for short transfers e.g. raising from bed and transfer to wheelchair,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1947-2012·2012-07-18

    Arjo Encore Mobile Patient Lifter Recalled for Exposed Metal Bracket Injury Risk

    ArjoHuntleigh is recalling specific Encore Mobile Patient Lifters because removing the knee pad assembly can expose a metal support bracket, posing an injury risk to patients.

    Product
    Encore Mobile Patient Lifter; manufactured by Arjo Ltd., St. Catherine Street, Gloucester, GL1 2SL, England, U.K.; Models KKB5022-21US and KKB5042-21US. The Encore is designed to be used as a standing and raising aid, it is useful for short transfers from one sitting position
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1948-2012·2012-07-18

    ArjoHuntleigh Recalls Chorus Mobile Patient Lifters Due to Injury Risk

    ArjoHuntleigh is recalling specific Chorus Mobile Patient Lifters because an exposed metal support bracket can cause injuries when the knee pad assembly is removed.

    Product
    Chorus Mobile Patient Lifter; manufactured by Arjo Ltd., St. Catherine Street, Gloucester, GL1 2SL, England, U.K.; Models KKB5060-21US, KKB5062-21US and KKB5080-21US. The Chorus is designed to be used as a standing and raising aid, it is useful for short transfers from one sit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·12V330000·2012-07-11

    Turtle Top Recalls Buses with Stuck Roof Hatches

    Turtle Top is recalling 361 commercial buses because roof hatches may be too hard to open in an emergency, potentially hindering passenger exit.

    Product
    TURTLE TOP — TURTLE TOP VANTERRA, TERRA TRANSPORT, ODYSSEY XL, ODYSSEY LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V323000·2012-07-09

    Van Hool Recalls 2011-2012 TD925 Motorcoaches for Driver Seat Defect

    Van Hool is recalling 152 model year 2011-2012 TD925 motorcoaches because an incorrect driver's seat riser and floor adapter plate were installed, increasing injury risk in a crash.

    Product
    VAN HOOL — VAN HOOL TD925
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1884-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannulas Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some cannula tips that can be dislodged.

    Product
    X-COATED SMALL PATIENT PACK Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during c
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1874-2012·2012-07-04

    Colgate 360 Toothbrush Heads Recalled Due to Battery Cap Defect

    Colgate-Palmolive is recalling 280,044 units of Colgate 360 Replaceable Head Battery Powered Bonus Twin Pack Toothbrushes because the battery cap can blow off.

    Product
    Colgate 360 Replaceable Head Battery Powered Bonus Twin Pack Toothbrush Soft UPC 03500068762 Dist. by Colgate-Palmolive Co. New York, NY 10022 Made in China. For teeth cleansing.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V307000·2012-06-29

    Zero Motorcycles Recalls 2011-2012 Models Due to Brake Light Switch Defect

    Zero Motorcycles is recalling certain 2011 and 2012 models because the front brake light switch may not activate until significant lever travel occurs, potentially failing to alert following drivers.

    Product
    ZERO — ZERO XD, XU, ZERO DS, ZERO XU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V322000·2012-06-26

    Campagna V13R Recalled for Improperly Installed Seat Belt Buckle Hardware

    Campagna is recalling 2011-2012 V13R three-wheel vehicles because the seat belt buckle assembly may have been installed with reversed hardware, potentially compromising occupant restraint.

    Product
    CAMPAGNA — CAMPAGNA V13R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V283000·2012-06-20

    Navistar Recalls 2013 International Durastar Trucks for Windshield Defect

    Navistar is recalling 1,298 2013 International Durastar trucks because windshield and backlight glass may separate from the cab, increasing the risk of injury or death.

    Product
    INTERNATIONAL — INTERNATIONAL DURASTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V262000·2012-06-08

    Blue Bird Recalls 2012 Buses Due to Roof Hatch Opening Issues

    Blue Bird is recalling 2012 All American and Vision non-school buses because roof hatches may not open easily in an emergency.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·12192·2012-06-05

    Evenflo Recalls Convertible High Chairs Due to Fall Hazard

    Evenflo is recalling about 35,000 convertible high chairs because the activity tray can detach, allowing unrestrained children to fall and sustain injuries.

    Product
    Convertible high chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·12V248000·2012-05-31

    Arboc Transit Buses Recalled for Roof Hatch Opening Force Defect

    Arboc is recalling 2011-2012 Freedom and Spirit of Mobility buses because roof hatches may not open easily in emergencies.

    Product
    ARBOC — ARBOC FREEDOM, SPIRIT OF MOBILITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·12185·2012-05-23

    Cooper Lighting Recalls Commercial Reflector Assemblies Due to Falling Hazard

    Cooper Lighting is recalling about 21,000 commercial reflector assemblies because they can fall from fixtures, posing an injury risk. No injuries have been reported.

    Product
    Portfolio 7-inch reflector assembly with glass lens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V228000·2012-05-22

    2012 Tiffin Phaeton Recalled for Air Brake System Non-Compliance

    Tiffin Motorhomes is recalling two 2012 Phaeton recreational vehicles because their air brake systems do not meet federal safety standards for park brakes.

    Product
    TIFFIN — TIFFIN PHAETON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·12180·2012-05-17

    Safety 1st Toilet and Cabinet Locks Recalled for Lock Failure

    Dorel Juvenile Group is recalling Safety 1st toilet and cabinet locks because they can be disengaged by young children, posing risks of drowning and injury.

    Product
    Toilet and Cabinet Locks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·12173·2012-05-09

    Kolcraft Bassinets Recalled by CPSC Due to Infant Fall Hazard

    Kolcraft is recalling about 46,000 Tender Vibes and Light Vibes bassinets because latches may fail, causing the bassinet to fall and injure an infant.

    Product
    Kolcraft Tender Vibes & Light Vibes bassinets
    Category
    Consumer Product
    Distribution
    Distributed nationwide