State
73,833 recalls have nationwide distribution and so reach Kansas. 5,822 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,822 recalls naming Kansas we have scored against our rubric, 1,053 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,486 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,822 recalls whose distribution notice names Kansas specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
MWT Materials, Inc. is recalling Accusorb MRI MAC7030 shielding blankets and covers because they may overheat and cause patient injury when not used correctly.
Pine Pharmaceuticals is recalling specific lots of Bevacizumab syringes for intravitreal use because they contain silicone oil microdroplets.
Lunera is recalling approximately 60,000 Helen GX23 LED lamps because they can overheat, posing fire, burn, and electric shock hazards. No injuries have been reported.
MWT Materials, Inc. is recalling 14 Accusorb MRI radio frequency shielding blankets and body-part covers because they may overheat and lead to patient injury when not used correctly.
GE Medical Systems is recalling two Aestiva 7900 ventilators because a stuck valve could cause excessive pressure and barotrauma.
GE Medical Systems is recalling 84 Aestiva MRI anesthesia systems because a drive gas check valve may become stuck open, potentially causing excessive pressure in the patient breathing circuit.
Freedom Pharmaceuticals is recalling specific lots of Baclofen USP powder because of the presence of a foreign substance.
Bluecar is recalling 2016 models because power train software may shut down power to the vehicle, increasing the risk of a crash.
MWT Materials, Inc. is recalling five units of Accusorb MRI Large Torso Wraps because they may overheat when not used correctly, posing a risk of patient injury.
GE Medical Systems is recalling certain Aisys and Avance anesthesia systems because a stuck valve could cause excessive pressure in the patient breathing circuit, potentially leading to barotrauma.
Grato Holdings is recalling Energique Shingles Pain & Ulceration Relief Topical Spray due to out-of-specification microbial counts. The recall covers 371 bottles distributed nationwide and to Guatemala and Canada.
Morton Grove Pharmaceuticals is recalling specific lots of Lindane Lotion because stability samples failed assay testing. Consumers should stop using the product and return it to their pharmacy.
Grato Holdings is recalling Energique homeopathic topical spray due to out-of-specification microbial counts. The product was distributed nationwide and to Canada and Guatemala.
Grato Holdings is recalling Energique Headache Pain & Sinus Pressure Relief Topical Spray due to microbial contamination.
Fukuda Denshi is recalling 95 DynaScope patient monitors in the US due to a potential short-term battery error caused by a damaged Lithium-Ion capacitor.
Innovasis is recalling two lots of Excella II titanium spine rods because they were packaged with each other's labels.
Valeant is recalling 1,178 SPAG-2 nebulizer units because serial ID labels and operation manuals contain incorrect or outdated information.
PD-Rx Pharmaceuticals is recalling 1,685 bottles of Phentermine Hydrochloride capsules because stability tests showed impurities exceeded specifications.
Altec Industries is recalling 2015 Effer 440 and 470 Knuckle Boom Cranes because pedestal welds may crack, potentially causing the crane to fall and injure people.
New Flyer is recalling specific 2009-2015 New Flyer and NABI buses because missing welds on seat brackets could allow seat belts to separate during a crash.
Terex is recalling 2011-2015 SCM48, SCM50, and SCM55 aerial devices because a defective leveling cylinder linkage can cause the platform to tilt, posing an injury risk.
ShowHauler is recalling 2007-2011 motorhomes, garage coaches, and toter coaches because electric entry steps may become unstable, increasing injury risk.
Ford is recalling 2004-2006 Ranger vehicles because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.
Takata is recalling driver-side air bag inflators in Audi, Ford, Mazda, Sprinter, and Volkswagen vehicles that may rupture during deployment.
Volkswagen is recalling 2011-2015 Touareg Hybrid vehicles because water in the battery tray may cause an electrical short and fire.