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.
Forest River is recalling specific 2015 Wildwood and 2016 Salem recreational trailers because the tire and wheel placard lists incorrect sizes, which could lead to vehicle instability if the wrong tires are installed.
PACCAR is recalling 2016 Peterbilt and Kenworth trucks because the transmission may lock or cause unexpected backward movement, increasing crash risk.
General Motors is recalling specific 2014-2015 Chevrolet and GMC trucks because the ignition lock actuator may bind, potentially causing loss of steering and braking power.
Starcraft RV is recalling 35 model year 2016 Autumn Ridge travel trailers due to an incorrectly built frame that may cause tire failure and increase crash risk.
Paccar is recalling specific 2011-2013 Peterbilt and Kenworth trucks because the fifth wheel locking mechanism may fail, potentially causing the trailer to detach.
General Motors is recalling 2014 Chevrolet Caprice and SS vehicles because a missing seat bracket may cause airbags to deploy with excessive force.
Hale Products Inc. is recalling certain firefighting vehicle pressure sensors that may display incorrect remaining agent levels, potentially increasing injury risk.
Ducati is recalling 2015-2016 Multistrada 1200 and 1200 S motorcycles because the side-stand may break, causing the bike to fall over and increasing injury risk.
Spartan Motors is recalling 1997-2005 MM and K2 motorhome chassis because a steering gear mounting bracket may crack, causing loss of steering.
Volvo is recalling 2012-2014 VNL trucks because Electric Auxiliary Power Units may detach, creating a road hazard and increasing crash risk.
KME is recalling 2013-2015 Predator emergency vehicles because loose front ball joints may separate, causing loss of steering control and increasing crash risk.
Tiffin is recalling 2014-2016 Breeze motorhomes because loose front suspension ball joints may separate, causing a loss of steering control.
Navistar is recalling specific 2016 International trucks because the engine control module may short circuit, causing the engine to stall without warning and increasing crash risk.
Safety 1st is recalling about 35,000 Décor Wood highchairs because children can remove the tray, posing a fall hazard. The company has received 68 reports of tray removal, including 11 injuries.
The Ice Cream Club, Inc. is recalling Caramel Caribou Ice Cream because it contains undeclared peanuts, a major food allergen.
Bed Handles Inc. is recalling approximately 113,000 portable bed handles sold without safety retention straps. The recall follows reports of four deaths caused by entrapment in gaps between the handle and mattress.
BMW is recalling specific 2014-2016 MINI and i3 vehicles because the passenger air bag may not deploy properly in a low-speed crash, increasing injury risk.
Hyundai is recalling 28,157 model year 2011 Elantra and Sonata vehicles because road salt may corrode front coil springs, potentially causing them to fracture and puncture tires.
Arrow International Inc. is recalling Arrow Kits containing Medtronic Covidien 0.9% Sodium Chloride Flush Syringes due to compromised sterility of the outer barrel.
MicroPort Orthopedics is recalling Profemur Plus modular neck hip prosthesis components due to an unexpected rate of postoperative fractures requiring revision surgery.
Volkswagen is recalling 993 model year 2015 Jetta, Golf, and E-Golf vehicles because the passenger air bag may not deploy properly in a crash.
Medistat RX L.L.C. is recalling all sterile products, including various injectable medications, due to a lack of assurance of sterility.
General Mills is recalling specific lots of Cascadian Farm Organic Cut Green Beans because one package tested positive for Listeria monocytogenes.
Biosense Webster is recalling SOUNDSTAR eco 8F and 10F Diagnostic Ultrasound Catheters because the ultrasound image may disappear if the CARTO 3 system restarts during a pericardial effusion.
Medtronic Navigation is recalling 2,346 Navigated Solera Screwdrivers used in spine surgery because specific use conditions may cause the tips to deform or break.