State
73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The Vitamin Shoppe is recalling Energy Formula Multivitamins because the packaging is not child-resistant, posing a poisoning risk to young children.
Subaru is recalling 2019 Impreza, Outback, Legacy, and Ascent vehicles because the low pressure fuel pump may fail, causing the engine to stall.
Polaris is recalling approximately 7,000 Model Year 2019-2020 Ranger XP 1000 and CREW XP 1000 off-road vehicles because a misrouted fuel line poses a fire hazard.
MTD Southwest is recalling specific Troy-Bilt, Craftsman, and Remington trimmers and polesaws because the heads can continue rotating after the throttle is released, posing a laceration hazard.
Polaris is recalling about 10,100 utility vehicles because seat belts may fail during a collision or tip-over, posing an injury hazard.
Wyndmere Naturals is recalling two essential oil products because they lack child-resistant packaging, posing a poisoning risk to young children.
Dr. Adorable is recalling Sweet Birch Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.
General Motors is recalling Rugger Liner hard tri-fold tonneau covers for 2019-2020 Chevrolet Silverado and GMC Sierra 1500 trucks because the attachment system may not secure the cover properly.
Ford is recalling 2020 Expedition vehicles because a front passenger seatbelt sensor may malfunction, potentially misclassifying the occupant and reducing crash protection.
Avet Pharmaceuticals is recalling Losartan Potassium Tablets 50 mg because FDA testing found an impurity above acceptable levels.
Siemens is recalling specific ONCOR radiation therapy systems due to a potential safety issue with dose monitoring interlocks that could result in a 10-20% overdose.
PharMEDium Services LLC is recalling 46 lots of nICARdipine HCl injection products because of a lack of sterility assurance.
PharMEDium Services is recalling 46 lots of rocuronium bromide syringes because of a lack of sterility assurance. The products were distributed nationwide in the US.
PharMEDium Services, LLC is recalling 46 lots of fentanyl citrate injection products due to a lack of sterility assurance.
PharMEDium Services is recalling 46 lots of ePHEDrine Sulfate syringes because the company could not ensure the products were sterile.
Zeiss is recalling a component for LSM 700, 800, and 900 microscopes because tilting the light arm can bypass laser safety, causing Class IIIB laser radiation emission.
PharMEDium Services is recalling 375 units of ePHEDrine Sulfate IV syringes because of a lack of sterility assurance.
Avet Pharmaceuticals is recalling Tetracycline Hydrochloride capsules due to out-of-specification dissolution results found during long-term testing.
PharMEDium Services is recalling 46 lots of Hydromorphone in 0.9% Sodium Chloride HCl syringes due to a lack of sterility assurance.
Siemens Medical Solutions is recalling specific MEVATRON radiation therapy systems due to a potential safety issue with dose monitoring interlocks that could result in a 10-20% radiation overdose.
PharMEDium Services, LLC is recalling 46 lots of fentanyl citrate injection products because of a lack of sterility assurance.
Siemens is recalling PRIMUS HI linear accelerators because a safety interlock defect could cause a 10-20% overdose of radiation therapy.
PharMEDium Services is recalling 46 lots of succinylcholine chloride syringes because of a lack of sterility assurance. The products were distributed nationwide in the US.
PharMEDium Services, LLC is recalling 46 lots of various IV products because of a lack of sterility assurance. The products were distributed nationwide in the US.
Avet Pharmaceuticals is recalling 17,524 bottles of Tetracycline Hydrochloride 500 mg capsules because they failed dissolution specifications during long-term testing.