State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mitsubishi is recalling 2015 Outlander Sport vehicles because a CVT hose clamp may not be secured, risking fluid leaks, inoperability, or fire.
Forest River is recalling 2017 Rockwood and Flagstaff trailers because the tire pressure placard lists 50 PSI instead of the required 65 PSI.
Pierce is recalling 2015-2016 Impel, Enforcer, and Velocity vehicles equipped with aerial devices because a plastic plug may separate, causing a hydraulic leak that disables the device.
Forest River is recalling 2016-2017 Surveyor recreational trailers because the Federal Placard incorrectly classifies them as school buses, posing a crash risk due to potential overloading.
House of Smoke is recalling approximately 4,692 pounds of Wild Boar Brotwurst because nitrite levels exceeded regulatory limits. No adverse reactions have been reported.
Pierce Manufacturing is recalling 2015-2016 Pumper and Tanker trucks because they lack required side marker lights, which may reduce visibility and increase crash risk.
Lorex is recalling Care 'N' Share video baby monitors because the lithium polymer batteries can overheat and swell, posing a burn risk.
Cycling Sports Group is recalling 2010-2012 Cannondale Bad Boy and Bad Girl commuter bicycles because the fork axle can crack, posing a fall hazard.
Nu Skin is recalling Epoch mist diffusers because mold can develop on the product, posing a health risk to individuals with compromised immune systems or mold allergies.
Crosman is recalling rope cocking devices for Centerpoint Sniper 370 crossbows because broken hooks can cause the rope to recoil, posing a laceration risk.
Dr. Praeger's Sensible Foods is voluntarily recalling frozen Black Bean Burgers because they may be contaminated with Listeria monocytogenes.
Dr. Praeger's is voluntarily recalling Organic Harvest Veggie Burgers because they may be contaminated with Listeria monocytogenes.
Dr. Praeger's Sensible Foods is voluntarily recalling specific lots of frozen Black Bean Burgers because they may be contaminated with Listeria monocytogenes.
Dr. Praeger's is voluntarily recalling California Veggie Burgers because they may be contaminated with Listeria monocytogenes.
Heartware, Inc. is recalling 18,631 HeartWare Ventricular Assist System batteries due to premature depletion. The recall covers devices distributed nationwide in the US.
Dr. Praeger's Sensible Foods is voluntarily recalling California Veggie Burgers because they may be contaminated with Listeria monocytogenes.
Pharmakon Pharmaceuticals is recalling Cefazolin 1GM syringes because the company cannot ensure the product is sterile.
Pharmakon Pharmaceuticals is recalling 10 bags of Magnesium Sulfate 1GM in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Medaus, Inc. is recalling B-Complex 50 in NaCl 0.9% vials because the company cannot assure the sterility of the product.
Pharmakon Pharmaceuticals is recalling 70 units of Bupivacaine HCI 0.25% bags because the company cannot assure the products are sterile.
Dr. Praeger's Sensible Foods is voluntarily recalling specific lots of Black Bean Veggie Burgers because they may be contaminated with Listeria monocytogenes.
Medaus, Inc. is recalling specific lots of L-Phenylalanine 15mg/mL vials because the FDA cannot assure the product is sterile.
Dr. Praeger's is voluntarily recalling Organic Harvest Veggie Burgers because they may be contaminated with Listeria monocytogenes.
Hospira is recalling 6,268 LifeCare Pump Model 4200 PCA Infusers because they may fail to detect distal occlusions, a defect that caused one serious injury.
Medaus, Inc. is recalling Manganese Sulfate vials because the company cannot guarantee the product is sterile. The recall covers vials distributed in the U.S., Japan, and New Zealand.