State
73,597 recalls have nationwide distribution and so reach Oklahoma. 5,818 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,818 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 5,818 recalls whose distribution notice names Oklahoma specifically. The 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Daimler Vans USA is recalling 2019-2020 Mercedes-Benz and Freightliner Sprinter vans because a brake pedal bolt may detach, causing brake lights to stay on and increasing crash risk.
Shanghai United Imaging Healthcare is recalling six X-ray systems because the tube head may move unexpectedly, posing a collision risk to patients.
Porsche is recalling certain 2021 Taycan, 911, Cayman, Boxster, and 718 Spyder models because suspension components may not have been properly tightened and could loosen, potentially causing loss of vehicle control.
Daimler Vans USA is recalling 2019-2020 Mercedes-Benz Sprinter vans with optional electric sliding doors because the auxiliary lock may be the incorrect type, potentially increasing injury risk in a crash.
Safety Belt Solutions is recalling specific seat belts because the tongues may not have been heat-treated correctly, potentially failing to restrain occupants in a crash.
Volkswagen Group (Audi) is recalling certain 2019-2021 Audi models for defective passenger air bags that may not deploy properly during a crash. Owners should contact Audi at 1-800-253-2834 for free inspection and repair.
BioFire Diagnostics is recalling BCID2 Panels due to a risk of false positive Pseudomonas aeruginosa results when used with specific BD BACTEC blood culture vials.
Baxter Healthcare is recalling PrisMax System Version II hemodialysis tubing due to performance variability that may cause alarms and therapy interruptions.
BMW is recalling certain 2021 XB7, X5, and X7 vehicles because the head restraints on second-row outer seats may be an incorrect type and could detach during a crash, increasing injury risk.
Lifetime Products is recalling 6-foot seminar tables because the brace arms may fail to lock, causing the table to collapse and posing an injury risk.
Hillsdale Furniture is recalling Jennings counter and bar stools because the seat can break off the base, posing a fall hazard.
Hyundai is recalling 2019-2021 Genesis G70 vehicles because the Anti-Lock Brake System module could short-circuit and cause an engine compartment fire. Owners should park outside until the ABS module fuse is replaced.
Siemens is recalling 37 Sensis Vibe systems in the US because they may sporadically freeze during operation or idle, preventing user interaction.
Teva Pharmaceuticals is recalling Metoclopramide Injection vials due to an unknown brown residue found inside one vial.
Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because the delivery system is out of specification for mechanical peel.
Noven Pharmaceuticals is recalling 551,670 Daytrana methylphenidate patches nationwide because the delivery system failed mechanical peel specifications.
Bovie Medical Corporation is recalling Velocity Disposable Bipolar Ablators because pinholes in the sterile packaging may compromise the sterile barrier.
Boston Scientific is recalling Captivator, Captiflex, and Sensation polypectomy snares because users reported incomplete pouch seals before use.
Noven Pharmaceuticals is recalling 473,280 Daytrana (methylphenidate) patches because the delivery system failed mechanical peel specifications.
Noven Pharmaceuticals is recalling 786,900 Daytrana (methylphenidate) patches because the delivery system failed mechanical peel specifications.
Bovie Medical Corporation is recalling 5,270 ConMed Disposable Bipolar Ablators because pinholes in the sterile packaging may compromise the sterile barrier.
Dr. Reddy's Laboratories is recalling 16,449 bottles of 200 mg Progesterone Capsules because stability testing revealed out-of-specification dissolution results.
G & H Wire Company is recalling orthodontic elastic bands because the patient pack text is incorrect, which could lead to misuse and temporary discomfort.
Bovie Medical Corporation is recalling 3,862 HNM Disposable Bipolar Ablators because pinholes in the sterile packaging may compromise the barrier.
Johnson & Johnson Surgical Vision Inc is recalling 27 TECNIS Toric 1-Piece Intraocular Lenses due to the release of nonconforming products.