The Recall Desk

State

Oklahoma product recalls

73,741 recalls have nationwide distribution and so reach Oklahoma. 5,822 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,822
Critical
1,040
Severe
1,493
Most recent
2026-10-28

Of the 5,822 recalls naming Oklahoma we have scored against our rubric, 1,040 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,493 (26%) are Severe.

These figures cover only the 5,822 recalls whose distribution notice names Oklahoma specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40351–40375 of 79563

  • HighNHTSA·18V566000·2018-08-28

    Blue Bird Recalls School Buses for Missing Child Restraint Warning Labels

    Blue Bird is recalling 2019-2020 Vision and All American school buses because certain child restraint seats may be missing a required warning label on the lower strap.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18762·2018-08-27

    Polaris Recalls 2018 RZR XP Turbo S Vehicles Due to ROPS Fracture Hazard

    Polaris is recalling about 1,300 model year 2018 RZR XP Turbo S recreational off-highway vehicles because the rollover protection structure can fracture during high-speed rollovers.

    Product
    Model year 2018 RZR XP Turbo S recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V565000·2018-08-27

    Fabform Recalls 2018 EPT Dump Trailers Due to Hinge Fracture Risk

    Fabform is recalling 2018 EPT dump trailers because welded hinges may fracture, causing the dump box to fall unexpectedly and increasing the risk of injury or death.

    Product
    FABFORM — FABFORM DUMP TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V564000·2018-08-27

    Jayco Recalls 2015-2017 Redhawk Motorhomes Due to Fire Risk

    Jayco is recalling 2015-2017 Redhawk motorhomes because liquid leakage into the driver's power window switch can cause corrosion and increase the risk of a fire.

    Product
    JAYCO — JAYCO REDHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·PHA-08242018-01·2018-08-24

    USDA Issues Public Health Alert for Empire Kosher Raw Chicken Due to Salmonella

    USDA FSIS issued a public health alert for Empire Kosher raw chicken products sold from September 2017 to June 2018 due to a link with a Salmonella outbreak.

    Product
    FSIS Issues Public Health Alert for Empire Kosher Poultry, Inc. Raw Chicken Products due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·18V563000·2018-08-24

    Navistar Recalls 2015-2019 IC Bus School Buses Due to Wheelchair Lift Defect

    Navistar is recalling 2015-2019 IC Bus school buses equipped with specific wheelchair lifts because a component may fail, allowing the platform to rise too high and increasing injury risk.

    Product
    IC BUS — IC BUS CESB, CASB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V559000·2018-08-23

    REV Recalls 2018-2019 Motorhomes Due to Generator Exhaust Fire Risk

    REV Recreation Group is recalling 2018-2019 Fleetwood Pulse and Holiday Rambler Prodigy motorhomes because the generator exhaust pipe may contact the waste tank, increasing fire risk.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD PRODIGY, PULSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V556000·2018-08-23

    RAM 1500 Recall for Rear Differential Oil Level Defect

    Chrysler is recalling 2018-2019 RAM 1500 trucks because the rear differential may be underfilled, which could cause axle failure and increase crash risk.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V561000·2018-08-23

    Thomas Built Buses Saf-T-Liner C2 School Bus Seat Recall

    Daimler Trucks North America is recalling 2017-2019 Thomas Built Buses Saf-T-Liner C2 school buses because seat mounting feet may pull through the floor joint in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V560000·2018-08-23

    Thomas Built Buses Recalling Wheelchair Lifts Due to Cam Failure

    Daimler Trucks is recalling 2015-2019 Thomas Built Buses equipped with specific wheelchair lifts because a component may fail, allowing the platform to rise too high.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·18199·2018-08-22

    Vornado VH101 Electric Space Heaters Recalled Due to Fire and Death

    Vornado Air is recalling VH101 Personal Vortex electric space heaters because they can overheat, posing fire and burn hazards. One death and 19 fire reports have been linked to the units.

    Product
    VH101 Personal Vortex electric space heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2824-2018·2018-08-22

    Sorin Platinium CRT-D Recall Due to Pacing and Sensing Loss

    Sorin CRM SAS is recalling 16 Platinium CRT-D devices because a hardware defect may cause loss of pacing and sensing, preventing the device from delivering necessary defibrillation.

    Product
    Sorin Platinium CRT-D 1711 DF-1, Sterile EO. Implantable Cardiac Defibrillator and Resynchronization Therapy Defibrillator
    Category
    Medical Device
    Distribution
    9 states
  • SevereFDA (Devices)·Z-2589-2018·2018-08-22

    Spacelabs Arkon Anesthesia Delivery System Recalled for Ventilation Failure Risk

    Spacelabs Healthcare is recalling 328 Arkon Anesthesia Delivery Systems because they may stop providing mechanical ventilation while in use or idle.

    Product
    Arkon Anesthesia Delivery System with Arkon Software Version 2.70, Display Unit Assembly 650-1769-00 installed, and Model #: 99999. This system includes a ventilator. The Spacelabs Arkon Anesthesia Workstation is intended for use in the hospital environment and operating…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2825-2018·2018-08-22

    Sorin Platinium CRT-D Recall Due to Loss of Pacing and Sensing

    Sorin CRM SAS is recalling 10 Platinium CRT-D devices because a hardware issue may cause loss of pacing and sensing, preventing the device from detecting arrhythmias.

    Product
    Sorin Platinium CRT-D 1741 DF-4, Sterile EO. Implantable Cardiac Defibrillator and Resynchronization Therapy Defibrillator
    Category
    Medical Device
    Distribution
    9 states
  • SevereNHTSA·18V554000·2018-08-22

    Volvo Recalls 2019 XC40 Vehicles Due to Brake Pedal Rivet Defect

    Volvo is recalling 2019 XC40 vehicles because brake pedals may not be correctly riveted, potentially reducing braking performance and increasing crash risk.

    Product
    VOLVO — VOLVO XC40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2793-2018·2018-08-22

    NxStage Express Fluid Warmer Recalled for Electrical Fire Risk

    NxStage Medical is recalling Express Fluid Warmers due to a potential risk of electrical fire if fluid leaks into the power receptacle.

    Product
    NxStage Express Fluid Warmer (FW-300, FW-300-A, FW-300-WW, FW-301, FW-301-A) Product Usage: The NxStage Express Fluid Warmer is an accessory to the NxStage System One used to warm therapy fluids prior to administration.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2832-2018·2018-08-22

    Beekley TomoSPOT Mammography Skin Markers Recalled for Imaging Artifacts

    Beekley Corporation is recalling TomoSPOT skin markers used in mammography because they may create imaging artifacts that mimic calcifications on patient mammograms.

    Product
    TomoSPOT REF 782, 782S, 783, 783S, 784, 784S, 785 & 785S Adhere to skin for marking and identifying moles in mammography.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2830-2018·2018-08-22

    Beekley O-SPOT REF 791 Mammography Markers Recalled for Imaging Artifacts

    Beekley Corporation is recalling O-SPOT REF 791 and 791S skin markers because they may create imaging artifacts that mimic calcifications on mammograms.

    Product
    O-SPOT REF 791, 791S Adhere to skin for marking and identifying moles in mammography.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2796-2018·2018-08-22

    Hamilton-C3 Ventilator Recalled Due to Control Board Component Defect

    Hamilton Medical AG is recalling two Hamilton-C3 ventilators because an out-of-specification control board component may cause the device to shut down and trigger alarms.

    Product
    Hamilton-C3 Ventilator Unit Product Usage: The HAMILTON-C3 ventilator is intended to provide positive pressure ventilator support to adults, pediatrics, infants and neonates depending on its configuration. The device is used in the intensive care ward, intermediate care…
    Category
    Medical Device
    Distribution
    9 states