State
73,737 recalls have nationwide distribution and so reach Oklahoma. 5,822 additional recalls listed Oklahoma specifically in their distribution scope.
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.
Which agencies issued them
These figures cover only the 5,822 recalls whose distribution notice names Oklahoma specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The Toro Company is recalling 2017-2019 LC922 towable log splitters because tow bolts may fail, causing the unit to detach or tip over.
Forest River is recalling 2018-2020 Cascade and Cherokee travel trailers because the trailer hitch coupler may fail, potentially causing the trailer to detach from the tow vehicle.
Jayco is recalling 2018-2020 Melbourne Prestige motorhomes because defective propane tank hangers may allow the tank to dislodge, increasing crash and fire risk.
Entegra is recalling 2018-2020 Qwest motorhomes because defective propane tank hangers may allow the tank to dislodge, increasing crash and fire risk.
Transportation Collaborative is recalling 2019-2020 TransTech school buses because the roof hatch handle may break, preventing emergency exit.
Harley-Davidson is recalling 2019-2020 FLRT and FLHTCUTG Trike motorcycles because faulty traction control software may activate a rear brake unexpectedly, increasing crash risk.
General Motors is recalling 2020 Cadillac, Chevrolet, and GMC vehicles because a missing fuel pump pressure regulator may cause over-pressurization and fire risk.
Navistar is recalling 2020 International HV 6X4 vehicles because a non-Quick Release Modulator Valve may increase brake release time, raising the risk of brake or tire fires.
Navistar is recalling specific International trucks because engaging the PTO switch can override the parking brake, causing unintended movement.
RESURRECTIONbeauty is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a poisoning risk to young children.
Jaguar Land Rover is recalling 2020 Range Rover Evoque vehicles because a metal plate on the headliner may detach during a crash, increasing injury risk.
Ford is recalling 2019 Ranger trucks because rear light connectors may be misaligned, causing lights to fail and increasing crash risk.
SCARPA is recalling Maestrale RS and Maestrale men's ski boots because the shells can crack, posing a fall hazard. No injuries have been reported.
Apotex Inc. is recalling Rite Aid Pharmacy Maximum Strength Ranitidine Tablets due to possible contamination with the impurity N-nitrosodimethylamine (NDMA).
Viatrexx Bio Incorporated is recalling Viatrexx-Articula vials because the manufacturing process cannot guarantee sterility. The product was distributed to physicians nationwide and in Puerto Rico.
Apotex Inc. is recalling Equate Maximum Strength Ranitidine Tablets due to possible contamination with the impurity N-nitrosodimethylamine (NDMA). The recall covers 1,132,453 bottles distributed nationwide.
Viatrexx Bio Incorporated is recalling Viatrexx-Ithurts sterile multi-dose vials because the manufacturing process cannot guarantee sterility.
Viatrexx Bio Incorporated is recalling Viatrexx-Infla vials because the manufacturing process cannot guarantee sterility. The product was distributed to physicians nationwide and in Puerto Rico.
Viatrexx Bio Incorporated is recalling Viatrexx-Collagen vials because the manufacturing process cannot guarantee sterility.
Viatrexx Bio Incorporated is recalling Viatrexx-Relief + sterile vials because the manufacturing process cannot guarantee sterility.
Heritage Medical Products is recalling 167 2000 Vascular beds due to a potential for the head of the bed to drop suddenly while a patient is lying on it.
Viatrexx Bio Incorporated is recalling 18 vials of Viatrexx-Immunexx because the manufacturing process cannot guarantee sterility.
Viatrexx Bio Incorporated is recalling Viatrexx-Male+ sterile vials because the manufacturing process cannot guarantee sterility.
Viatrexx Bio Incorporated is recalling Viatrexx-Connectissue vials because they were manufactured in a manner that cannot guarantee sterility.
Apotex Inc. is recalling Rite Aid Pharmacy Maximum Strength Ranitidine Tablets due to possible contamination with the impurity N-nitrosodimethylamine (NDMA).