State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Grandma's Herbs is recalling Cholesterol Support dietary supplements because they contain undeclared soy lecithin, a common allergen.
Handi-Craft is recalling Dr. Brown's Natural Bottle & Dish Soap because it may contain harmful bacteria. No injuries have been reported.
Lakeside Foods, Inc. is recalling 1,856 cases of IQF green beans in 17 states due to potential Listeria monocytogenes contamination.
Medtronic Navigation is recalling 277 reusable ENT suction instruments because they fail pre-use verification checks. The devices are used with the StealthStation AxiEM surgical navigation system.
Alcon is recalling 367 ORA Systems with VerifEye because a software error may cause incorrect intraocular lens power measurements during cataract surgery.
Shippert Medical Technologies is recalling Tissu-Trans Filtron 100 units because the seal integrity of the sterile packages cannot be assured.
Medtronic is recalling eight AxiEM ENT suction kits because the instruments fail mandatory pre-use verification tests.
Medtronic is recalling 15 Fusion ENT Instrument Kits because the instruments fail pre-use verification. The kits were distributed in the US and Canada.
C. O. Truxton is recalling specific lots of Phenobarbital Tablets USP, 60 mg, due to a label mixup that may result in mislabeling.
C. O. Truxton is recalling Phenobarbital Tablets USP, 100 mg, due to a label mixup that may result in mislabeled products.
Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 500 because the seal integrity of the sterile packages cannot be assured.
Medtronic is recalling 13 reusable ENT instrument sets because they fail required pre-use verification checks. The devices are used with the StealthStation AxiEM surgical navigation system.
Pentax of America Inc is recalling 116 ultrasound video gastroscopes because the instructions for use contain an error in the disinfection step.
C. O. Truxton is recalling specific lots of Amitriptyline HCL 50 mg tablets due to potential label mixups. The recall is nationwide.
Medtronic is recalling 75 Curved Suction 90 ENT instruments because they fail required pre-use verification checks.
PD-Rx Pharmaceuticals is recalling 3,440 bottles of Phentermine Hydrochloride capsules because stability tests showed out-of-specification unknown impurities.
Pentax of America Inc. is recalling 118 ultrasound video gastroscopes because the instructions for use contain an error in the disinfection step.
C. O. Truxton is recalling specific lots of Phenobarbital Tablets USP, 15 mg, due to a label mixup that may result in mislabeled products.
Autocar is recalling 85 Xpeditor vehicles because a steering component may loosen, potentially causing a complete loss of steering and increasing crash risk.
Crane Carrier is recalling 2015-2016 LET2 vehicles because a loose tie rod could cause complete loss of steering.
Autocar is recalling 2016 Xpert and Xspotter vehicles because a loose tie rod could cause a complete loss of steering and increase crash risk.
Volvo is recalling 2016 VNL and VNM trucks because a loose tie rod may cause complete loss of steering, increasing crash risk.
Fabri-Tech is recalling about 6,500 infant shortall rompers sold at Cracker Barrel because shoulder buttons can detach, posing a choking hazard to children.
KME is recalling 2016 Predator Pumper, Rescue, and Airport Refueler vehicles because a loose tie rod could cause a complete loss of steering.
Ford is recalling certain wheel hub bearing assemblies for 2011-2017 Ford Explorer 4X2 vehicles because they lack a self-retention feature, which could cause the wheel to separate.