State
73,827 recalls have nationwide distribution and so reach Oklahoma. 5,823 additional recalls listed Oklahoma specifically in their distribution scope.
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.
Which agencies issued them
These figures cover only the 5,823 recalls whose distribution notice names Oklahoma specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Jaguar Land Rover is recalling 856 model year 2015 Range Rover and Range Rover Sport vehicles because the second row seat back may not latch properly, increasing injury risk in a crash.
Honda is recalling 2014-2015 Accord Hybrid vehicles because electrical interference may cause the hybrid system to fail, limiting speed and potentially stalling the vehicle.
Merhow is recalling 2006-2013 Horse Trailers because a door lock defect may jam the deadbolt, potentially trapping occupants inside the vehicle.
Paccar is recalling 354 model year 2016 Kenworth and Peterbilt trucks because a short circuit in the engine control module may cause the engine to stall without warning.
Forest River is recalling 2011-2016 Glaval Titan II buses because a screw may have pierced the exhaust tube, posing a fire and fume risk.
General Motors is recalling specific 2006-2007 Buick, Chevrolet, and GMC SUVs because fluid in the power window switch module can cause a short circuit and fire.
Rainbow Play Systems is recalling yellow plastic trapeze rings that can crack or break, posing a fall hazard to children.
Chrysler is recalling 2016 Town and Country and Dodge Grand Caravan minivans because hood striker bolts may loosen, allowing the hood to open while driving.
Fujitsu America is recalling specific lithium-ion battery packs for notebook computers because they can overheat and catch fire. Consumers should remove the battery and contact Fujitsu for a free replacement.
E-One is recalling 2013-2014 Typhoon, Cyclone II, and Quest emergency vehicles because loose front suspension ball joints could separate, causing loss of steering control.
Wishbone Design is recalling Recycled Edition Bikes because the handlebar can pinch fingers. The company reported four incidents, including two injuries requiring medical attention.
Pride Family Brands is recalling Bed Bath & Beyond Destination Summer Hammock Stands because the Z-shaped hooks can bend or break, causing consumers to fall.
Lippert is recalling Coachstep Double and Triple Electric Steps because a bolt may fracture, causing the steps to become unstable and increasing the risk of injury.
SynCardia Systems is recalling Freedom Drivers because a component may fail, causing the drive mechanism to stop pumping and resulting in the loss of life-sustaining function.
The Compounding Pharmacy of America is recalling Fentanyl and Bupivacaine Intrathecal Solution due to FDA inspection findings of GMP violations that may impact sterility.
The Compounding Pharmacy of America is recalling Testosterone 70 mg sterile pellets due to FDA inspection findings of GMP violations that may impact sterility.
FCA is recalling 2016 Ram 2500, 3500, 4500, and 5500 trucks because a short circuit in the Engine Control Module may cause the engine to stall without warning, increasing crash risk.
The Compounding Pharmacy of America is recalling Fentanyl and Bupivacaine Intrathecal Solution due to FDA inspection findings of GMP violations that may impact sterility.
The Compounding Pharmacy of America is recalling Estradiol 15 mg sterile pellets nationwide because FDA inspections identified GMP violations affecting sterility.
The Compounding Pharmacy of America is recalling Hydromorphone and Bupivacaine Intrathecal Solution due to FDA inspection findings of GMP violations that may impact sterility.
The Compounding Pharmacy of America is recalling Tri-Mix Super Injectable vials because FDA inspections found violations that may affect sterility.
The Compounding Pharmacy of America is recalling Sufentanil and Bupivacaine solution because FDA inspections found violations that may have compromised sterility.
The Compounding Pharmacy of America is recalling PGE 40 (Alprostadil) 40 mcg/ml Injection due to FDA inspection findings of GMP violations that may impact sterility.
The Compounding Pharmacy of America is recalling specific lots of compounded intrathecal solution due to FDA inspection findings of GMP violations that may impact sterility.
The Compounding Pharmacy of America is recalling Baclofen 1,000 mcg/ml Intrathecal Solution due to FDA inspection findings of GMP violations that may impact sterility.