The Recall Desk

State

Oklahoma product recalls

73,806 recalls have nationwide distribution and so reach Oklahoma. 5,823 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,823
Critical
1,040
Severe
1,494
Most recent
2026-11-04

Of the 5,823 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 1,494 (26%) are Severe.

These figures cover only the 5,823 recalls whose distribution notice names Oklahoma specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42376–42400 of 79629

  • SevereNHTSA·18V208000·2018-03-29

    Mercedes-Benz Recalls 2018 Models for Driver Air Bag Inflator Defect

    Mercedes-Benz is recalling 2018 AMG GT, AMG GT C, GLC43 AMG, GLC300, and GLC350e vehicles because defective steel in the driver-side air bag inflator housing may cause rupture during deployment.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 350 E, GLC 300, AMG GLC43, AMG GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V203000·2018-03-29

    Alfa Romeo Stelvio Recall for Liftgate Wiring Water Leak

    FCA US LLC is recalling 2018 Alfa Romeo Stelvio vehicles because water leaks into liftgate wiring, causing corrosion that may allow the liftgate to open while driving.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V206000·2018-03-29

    Spartan Gladiator Recall for Front Axle Spindle Failure Risk

    Spartan Motors is recalling 2004-2007 Gladiator emergency response vehicles because front axle spindles may crack and fail, potentially causing a wheel to separate.

    Product
    SPARTAN — SPARTAN GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V199000·2018-03-29

    Navistar Recalls 2018-2019 International LT Trucks for Fuel Leak Risk

    Navistar is recalling 2018-2019 International LT trucks because a fender splash panel may rub against the fuel line, causing a leak that could lead to fire or crash.

    Product
    INTERNATIONAL — INTERNATIONAL LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E017000·2018-03-29

    Timoney Front Suspension Recall Due to Axle Spindle Fatigue Cracks

    Timoney Technology is recalling Mark 1 and Gen 2 Independent Front Suspensions because inconsistent machining may cause axle spindle failure and wheel separation.

    Product
    SUSPENSION:FRONT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V204000·2018-03-29

    Tesla Recalls Model S Vehicles Due to Steering Bolt Corrosion Risk

    Tesla is recalling 2012-2016 Model S vehicles because aluminum steering bolts may corrode and fracture, potentially causing a loss of power steering assist.

    Product
    TESLA — TESLA MODEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18733·2018-03-29

    Residential Elevators Recalls Traction Elevators Due to Impact Hazard

    Residential Elevators Inc. is recalling about 3,700 traction elevators installed in homes between January 2015 and April 2017 because the cab can rise unexpectedly to the top of the shaft, posing an impact hazard.

    Product
    Traction elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V207000·2018-03-29

    Mercedes-Benz Recalls 2017-2018 Models Due to Front Seatback Locking Defect

    Mercedes-Benz is recalling specific 2017-2018 C-Class and E-Class vehicles because front seatbacks may not lock properly, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 400, C 300, AMG C63S, AMG C43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V205000·2018-03-29

    Alfa Romeo Stelvio Recall for Water-Induced Electrical Corrosion

    FCA US LLC is recalling 2018 Alfa Romeo Stelvio vehicles because water leaks into the body control module, causing electrical malfunctions that increase crash risk.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18734·2018-03-29

    Octane Fitness Recalls XT-One Elliptical Cross Trainers Due to Fall Hazard

    Octane Fitness is recalling about 570 XT-One elliptical cross trainers because the incline lead screw can shear off, causing foot pedals to drop unexpectedly and creating a fall hazard.

    Product
    Octane Fitness XT-One elliptical cross trainers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18132·2018-03-29

    Primo Recalls hTrio Beverage Dispensers Due to Burn Hazard

    Primo is recalling hTrio beverage dispensers because hot water may leak at high altitudes, posing a burn risk.

    Product
    Primo hTrio Multi-purpose beverage dispensers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1122-2018·2018-03-28

    MedComp Recalls 12F Tesio Catheter Sets Due to Connection Failure Risk

    Medical Components, Inc. is recalling 385 12F Tesio Catheter Sets because connection failures may cause blood loss or air emboli.

    Product
    12F Tesio CATHETER SET (CUFF 22CM FROM TIP), REF MCTC1235SD, UDI 884908027242 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1127-2018·2018-03-28

    MedComp Repair Kit Recalled for Potential Connection Failures and Blood Loss Risk

    Medical Components, Inc. is recalling 1,575 MedComp Repair Kits due to potential connection failures that could lead to blood loss or air emboli.

    Product
    REPAIR KIT, REF RPK-01, UDI 884908039856 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1124-2018·2018-03-28

    MedComp Recalls 12F Tesio Catheter Sets Due to Connection Failure Risk

    Medical Components, Inc. is recalling 12F Tesio Catheter Sets because connection failures may cause blood loss or air emboli.

    Product
    12F Tesio CATHETER SET (CUFF 32CM FROM TIP), REF MCTC1247SD, UDI 884908027266 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1118-2018·2018-03-28

    MedComp Recalls Catheter Repair Kits Due to Connection Failure Risk

    Medical Components, Inc. is recalling 93 Catheter Repair Kits because potential connection failures could lead to blood loss or air emboli.

    Product
    CATHETER REPAIR KIT, REF AAC52001, UDI 884908001891 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V201000·2018-03-28

    LGS Recalls 2018 Pace, Look, and Cargo Express Cargo Trailers

    LGS Industries is recalling 2018 Pace, Look, and Cargo Express cargo trailers because a spindle weld on the axle may fail, potentially causing loss of vehicle control.

    Product
    LOOK — LOOK, PACE, CARGO EXPRESS CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1100-2018·2018-03-28

    Boston Scientific Recalls Malecot Nephrostomy Catheters Due to Breakage

    Boston Scientific is recalling Malecot Nephrostomy Catheter Sets because they may break at the mid-shaft bond during use.

    Product
    Malecot Nephrostomy Catheter Set, Product Number: M0064101000, GTIN: 08714729005261 The Malecot Nephrostomy Catheter Set is intended to establish percutaneous nephrostomy drainage and is indicated for the following: Diagnostic Indications: " Antegrade pyelography "…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1125-2018·2018-03-28

    MedComp Two Part Adapter Recall for Potential Connection Failures

    Medical Components, Inc. is recalling 35 MedComp Two Part Adapter kits due to potential connection failures that could cause blood loss or air emboli.

    Product
    TWO PART ADAPTER, REF MCTLA2000, UDI 884908027310 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1139-2018·2018-03-28

    BD Vacutainer Tubes Recalled for Lead Test Inaccuracy

    Becton Dickinson is recalling specific Vacutainer tubes because they may cause underestimation of lead levels in blood samples when used with certain assays.

    Product
    BD Vacutainer¿ EDTA Lavender Top Tubes: Catalog Numbers: 1. 366401 (UDI: 50382903664011); 2. 366450 (UDI: 50382903664509); 3. 366643 (UDI: 50382903666435); 4. 367835 (UDI: 50382903678353); 5. 367841 (UDI: 50382903678414); 6. 367844 (UDI: 50382903678445); 7. 367856 (UDI…
    Category
    Medical Device
    Distribution
    47 states
  • SevereFDA (Devices)·Z-1133-2018·2018-03-28

    Boston Scientific Recalls SpyScope DS Biliary Catheters Due to Sleeve Defect

    Boston Scientific is recalling 5,026 units of SpyScope DS Access and Delivery diagnostic biliary catheters because a sleeve may protrude, causing tissue damage or bleeding.

    Product
    SpyScope DS Access and Delivery diagnostic biliary catheter, M00546600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·026-2018·2018-03-28

    Tony Downs Recalls Chicken Products Due to Possible Plastic Contamination

    Tony Downs Foods is recalling approximately 96,384 pounds of canned chicken breast products that may contain hard plastic. The recall was initiated after two consumer complaints regarding foreign matter.

    Product
    Tony Downs Foods — Tony Downs Food Company, Inc. Recalls Chicken Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·18732·2018-03-28

    Shop LC Recalls Electric Blankets Due to Fire and Burn Hazards

    Shop LC is recalling electric heated throw blankets because the heating coils can overheat, posing fire and burn hazards.

    Product
    Electric heated micro plush flannel sherpa throw blankets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1141-2018·2018-03-28

    BD Vacutainer Tubes Recalled for Lead Test Inaccuracy

    Becton Dickinson is recalling specific Vacutainer tubes because they may cause underestimation of lead in blood samples when used with certain assays.

    Product
    BD Vacutainer¿ EDTA Pink Top Tube; Catalog Numbers: 1. 367842 (UDI: 50382903678421); 2. 367899 (UDI: 50382903678995); 3. 368049 (UDI: 50382903680493); 4. 368589 (UDI: 50382903685894)
    Category
    Medical Device
    Distribution
    47 states
  • SevereFDA (Devices)·Z-0194-2018·2018-03-28

    Monteris Medical Recalls NeuroBlate Systems Due to MRI Interaction

    Monteris Medical Corp is recalling 52 NeuroBlate systems used for MRI-guided neurosurgery due to an unanticipated interaction with 1.5 Tesla MRI systems.

    Product
    MONTERIS MEDICAL NEUROBLATE SYSTEM, used for MRI-guided neurosurgical ablation.
    Category
    Medical Device
    Distribution
    Distributed nationwide