State
72,940 recalls have nationwide distribution and so reach Oklahoma. 5,788 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,788 recalls naming Oklahoma we have scored against our rubric, 1,033 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,238 (21%) are Severe.
Which agencies issued them
These figures cover only the 5,788 recalls whose distribution notice names Oklahoma specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
C.R. Bard is recalling 116 Bard InLay Optima Ureteral Stent Kits, 6 Fr x 14 cm, because the actual stent size may not match the product label.
Orthofix U.S. is recalling 40,956 CONSTRUX Mini Ti Spacer System units because the labeling contains claims that are not consistently present.
Orthofix U.S. is recalling 13,317 Pillar SA PTC Spacer System units because the labeling contains claims that are not consistently present.
Orthofix U.S. is recalling 19,431 FIREBIRD SI Fusion System units because the labeling contains claims that are not consistently present.
Cardinal Health is recalling 251,165 ChemoPlus gowns and sleeves because the packaging shows a five-year shelf life when the product's actual shelf life is three years.
Winder Laboratories is recalling 3,528 bottles of Morphine Sulfate Oral Solution because the size stated on the carton label did not match the size of the bottle inside.
C.R. Bard is recalling 4,350 BD InLay Optima Ureteral Stent Kits, 4.7 Fr x 26 cm, because the actual stent size may not match the product label.
Stryker is recalling 294 MV3 bariatric beds because they and Arise 1000EX mattresses have been sold in close proximity, and the two products have not been tested for compatibility.
Steris is recalling 10 AMSCO 7052HP Washer/Disinfectors because a wire connected to the electrical box may shift out of position, which may result in electrical arcing inside the unit.
Stryker is recalling 297 Arise 1000EX mattresses because they and certain MV3 beds have been sold in close proximity, and the two products have not been tested for compatibility.
Lupin Pharmaceuticals is recalling 52,128 bottles of Sertraline Hydrochloride Tablets, 100 mg, over a defective container in which the seal is not adhering to the bottles.
C.R. Bard is recalling 116 BD InLay Optima Ureteral Stent Kits, 8 Fr x 26 cm, because the actual stent size may not match the product label.
Cipla USA is recalling 1,180 boxes of Lanthanum Carbonate chewable tablets, 1000mg, from a further lot after an out of specification hardness test result.
Fagron Compounding Services is recalling 2,980 syringes of a compounded topical ophthalmic solution over an incorrect product formulation.
Orthofix U.S. is recalling 14,201 Forza Ti Spacer System units because the labeling contains claims that are not consistently present.
Datascope is recalling 47 Cardiosave Rescue Intra-Aortic Balloon Pump systems to issue an instructions for use addendum revising the preventative maintenance schedule.
Datascope is recalling 11,470 Cardiosave Hybrid Intra-Aortic Balloon Pump systems to issue an instructions for use addendum revising the preventative maintenance schedule.
Toyota is recalling certain 2025-2026 Camry Hybrid and 2026 Corolla Cross Hybrid vehicles because a bolt inside the inverter may not be tightened properly, causing incomplete contact at the terminal.
Gillig is recalling 2025 Low Floor transit buses because wheelchair restraints may fail to lock, posing an injury risk.
Mack Trucks is recalling 2010-2016 Granite trucks because incorrect parts from a previous repair may cause brake overheating, increasing the risk of tire blowouts or fires.
Gillig is recalling 2013 Low Floor transit buses because emergency exit window latches may fail during a crash, increasing injury risk.
Suzanna's Kitchen is recalling fully cooked breaded chicken products because they contain soy, a known allergen, that is not declared on the label.
Ford is recalling 2022-2025 E-Transit vehicles because the left rear axle half shaft may disengage, causing loss of drive power or vehicle rollaway.
Ford is recalling 6,819 model year 2026 Super Duty F-250 and F-350 vehicles because the right rear axle shaft may have been improperly heat-treated and may break.
Diamond Coach is recalling 2025 VIP buses because wheelchair restraints may fail to lock, increasing injury risk during transit.