State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Lance Camper is recalling 2019-2020 855S and 1172 Truck Campers because a gap in the fold-down bunk bed may allow occupants to fall and get stuck.
Unruh Fire is recalling one 2018 RAM 5500-based fire truck because its brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.
Forest River is recalling 2019-2020 R-POD travel trailers because a refrigerator wire may be connected to a breaker that allows too much current, increasing the risk of fire.
Forest River is recalling 2018-2019 Cherokee travel trailers because the Federal Placard may list incorrect axle and capacity information, potentially leading to vehicle overload.
South Shore is recalling Libra style 3-drawer chests due to tip-over and entrapment hazards that have resulted in one fatality and one injury.
Chrysler is recalling specific Ram 1500, 2500, and 3500 pickup trucks because a tailgate latch component may fracture, causing the tailgate to open while driving and creating a road hazard.
Jaguar Land Rover is recalling 2016-2017 Range Rover and Range Rover Sport vehicles because the driver's seat belt may not lock properly during braking, increasing injury risk.
BMW is recalling 2016-2019 X1 vehicles because the B-pillar may not absorb impact adequately in a crash, increasing injury risk.
Jaguar is recalling 2019-2020 I-PACE vehicles because a regenerative brake failure can delay deceleration, increasing crash risk.
Chrysler is recalling 2017-2019 Pacifica vehicles with stop/start systems because a loose battery ground connection may cause power steering loss or stalling, increasing crash risk.
Imagine Nation Books is recalling wireless charging pads that can overheat and cause burns or damage to furniture and bedding.
Stainless & Repair is recalling certain 1994-1995 Ford L9000 and 2016-2017 Freightliner M2-112 trucks equipped with Whelen brake lights that may illuminate without the brake pedal being pressed.
Havertys is recalling Beckley Entertainment Hutches because the top shelf can fall, posing an injury hazard. The company has received 12 reports of the shelf falling, including two minor injuries.
BMW is recalling specific 2019-2020 models because knee air bag assemblies may be improperly folded and assembled. This defect could prevent the air bags from deploying as intended, increasing the risk of injury.
Hercules Candy Company is recalling 15 bags of Cashew Brittle Bits because they may contain undeclared peanuts. Consumers should stop eating the product.
Customceutical Compounding is recalling 8 vials of Test D compounded injectable due to a lack of assurance of sterility. The product was distributed nationwide.
Torrent Pharma Inc. is recalling Losartan Potassium Tablets, 100 mg, because FDA labs confirmed the presence of the impurity NMBA above acceptable levels.
Philips is recalling Fetal Spiral Electrodes because the metal tip may break off and remain in a newborn's scalp during delivery.
Torrent Pharma Inc. is recalling Losartan Potassium Tablets because FDA labs found an impurity above acceptable levels.
Customceutical Compounding is recalling TriMix MEDIUM injectable compound due to a lack of assurance of sterility. The product was distributed nationwide.
Baxter Healthcare is recalling 158 SIGMA Spectrum Infusion Pumps because flow rate tests were performed for less than the required time, potentially leading to inaccurate fluid administration.
Customceutical Compounding is recalling 16 vials of Lipoplex injectable compound because the sterility of the product cannot be assured.
AvKARE Inc. is recalling Losartan Potassium Tablets 50 mg because FDA testing found an impurity above acceptable levels.
Customceutical Compounding is recalling 19 vials of BPlex injectable compound due to a lack of assurance of sterility. The product was distributed nationwide.
Torrent Pharma Inc. is recalling Losartan Potassium and Hydrochlorothiazide Tablets because FDA labs found an impurity above acceptable levels.