State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Tiffin is recalling 2017 Allegro Open Road motorhomes because the tow hitch sticker lists incorrect weight capacities, which could lead to hitch failure.
General Motors is recalling 2017 Buick LaCrosse vehicles because water may enter the electric power steering connectors, potentially causing a loss of power steering.
BMW is recalling 2017 430i, 440i, M4, and Rolls-Royce Dawn vehicles because seat-mounted air bag inflator initiators may fail to ignite during a crash.
STIHL is recalling about 100,000 gas-powered chain saws because a leaking fuel line can cause fire and burn hazards. Consumers should stop using the saws and return them for a free repair.
Mercedes-Benz is recalling 307,629 vehicles because repeated starter attempts may overheat a component, increasing the risk of a fire.
Ready Pac Foods is recalling approximately 59,225 pounds of Puro Picante Blazin Hot chicken salad due to possible Listeria monocytogenes contamination. No illnesses have been reported.
GE Healthcare is recalling 60 Discovery MR450 MRI scanners because a component failure can cause the patient bore to heat up, potentially leading to serious burns.
Integra LifeSciences Corp. is recalling 944 units of the Cadence Total Ankle System because posterior tibial fractures have been reported.
Physio-Control is recalling 338 LIFEPAK 15 defibrillators because an internal relay may fail, preventing the device from delivering defibrillation energy.
Mako Surgical Corporation is recalling 595 Stryker Restoris RIO Reamer Handles because they may fail to engage mating components during surgery.
Zimmer Biomet is recalling 4,388 Comprehensive Reverse Shoulder System Humeral Trays because they are fracturing at higher-than-anticipated rates, posing a risk of revision surgery.
Fratelli Beretta USA is recalling approximately 468 pounds of Deli Thin Dietz & Watson Mortadella because the product contains undeclared pistachio nuts, a known allergen.
Argon Medical Devices is recalling specific bone marrow aspiration needles because a potential defect in the blister packaging may compromise the sterility of the product.
Aesculap Implant Systems LLC is recalling 24 GN200 Caiman HF generators due to a faulty component that may impact proper device functioning.
Atrium Medical Corporation is recalling Maquet Ocean Water Seal Chest Drains because the manual vent valve may fail to re-seal after use.
Atrium Medical Corporation is recalling Maquet Express Dry Seal Suction OCEAN DRAIN chest drains because the manual vent valve may fail to re-seal after use.
Calphalon is recalling approximately 2 million Contemporary Cutlery knives because blades can break during use, posing a laceration hazard.
Encore Medical is recalling 13 LIMA Modular Revision Hip Stems because they were inadvertently re-sterilized, which may compromise the integrity of the safety screw.
Moose Toys is recalling Little Live Pets Lil Frog toys because the battery cap can become a projectile and chemicals can leak, causing eye irritation.
Argon Medical Devices is recalling T-LOK bone marrow biopsy needles due to a potential defect in the blister packaging that may compromise sterility.
Advanced Sterilization Products is recalling STERRAD NX Sterilization Systems because the door interlock may disengage for 20 seconds after a power outage.
Atrium Medical Corporation is recalling Maquet Express Dry Seal Suction chest drains because the manual vent valve may fail to re-seal after being depressed.
Merge Healthcare is recalling Schiller PB 1000 blood pressure pumps because insufficient voltage causes them to fail before reaching adequate pressure.
Atrium Medical is recalling Maquet Ocean Water Seal Chest Drains because the manual vent valve may fail to re-seal after being depressed.
Atrium Medical is recalling Maquet Oasis chest drains because the manual vent valve may fail to re-seal after use.