State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Qualgen, LLC is recalling Estradiol 6 mg pellets nationwide because the company cannot ensure the product is sterile.
Qualgen, LLC is recalling Estradiol 25mg pellets because the company cannot assure the sterility of the product. The recall covers specific lots distributed nationwide.
ICU Medical is recalling 5% Dextrose Injection bags because they may lack sterility and have the potential to leak.
Silver Star Brands is recalling 247 bottles of Healthful Naturals DizziFree Oral Spray due to manufacturing deviations that could result in microbial contamination.
Qualgen, LLC is recalling Estradiol 12.5mg pellets nationwide because the company cannot ensure the product is sterile.
ICU Medical is recalling 2,580,448 bags of 0.9% Sodium Chloride Injection because they may leak and lack assurance of sterility.
Valley Processing Inc. is recalling specific lots of apple juice concentrate and organic apple juice concentrate because they contain high levels of inorganic arsenic.
Qualgen, LLC is recalling Testosterone 200 mg/Anastrozole 20 mg pellets due to a lack of assurance of sterility. The recall affects specific vial sizes distributed nationwide.
Request Foods Incorporated is recalling Beecher's Enchilada Bowl Verde due to potential contamination with Listeria monocytogenes and Salmonella.
Qualgen, LLC is recalling specific lots of Testosterone 50mg pellets nationwide due to a lack of assurance of sterility.
GE Healthcare is recalling 73 Centricity Universal Viewer units because a synchronization failure may affect the display of medical images.
Request Foods Incorporated is recalling Evol Truffle Parmesan & Portabella Risotto because ingredients may be contaminated with Listeria monocytogenes and Salmonella.
Request Foods Incorporated is recalling Kashi Fire Roasted Quinoa Bowls because ingredients may be contaminated with Listeria monocytogenes and Salmonella.
Request Foods Incorporated is recalling Udi's Broccoli & Kale Lasagna because ingredients may be contaminated with Listeria monocytogenes and Salmonella.
Zimmer Biomet is recalling 23,726 RapidFlap SpinDown Clamps because the nut was assembled incorrectly. The device is used to re-attach bone flaps after craniotomy.
Trident Seafoods is recalling Kroger brand frozen Alaskan Salmon Bites due to potential contamination with Listeria monocytogenes or Salmonella in the vegetable ingredient.
Blue Bird is recalling 2007-2019 All American ambulance buses because stretcher clamps may fail, increasing injury risk.
Request Foods Incorporated is recalling Udi's Pesto Tortellini because ingredients may be contaminated with Listeria monocytogenes and Salmonella.
Request Foods Incorporated is recalling Kashi Pesto Chickpea Quinoa Bowls because ingredients may be contaminated with Listeria monocytogenes and Salmonella.
AROA Biosurgery is recalling 8,853 boxes of Endoform Dermal Template 2x2 due to a potential pouch seal failure that could compromise sterility.
Request Foods Incorporated is recalling Evol Portabello Goat Cheese Ravioli because ingredients may be contaminated with Listeria monocytogenes and Salmonella.
Ford is recalling 2019 Lincoln Nautilus vehicles because the driver's air bag cover may detach during deployment, increasing injury risk.
Cordis Corporation is recalling 162 units of POWERFLEX PRO PTA Dilatation Catheters because they may not meet internal manufacturing burst strength specifications.
Zimmer Biomet is recalling 3,246 RapidFlap SpinDown Clamps because the nut was assembled incorrectly. The device is used to re-attach bone flaps after craniotomy.
Qualgen, LLC is recalling Testosterone 12.5mg pellets nationwide because the sterility of the product cannot be assured. Consumers should stop using the affected lots and contact the manufacturer or pharmacist.