State
73,809 recalls have nationwide distribution and so reach Indiana. 9,598 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,598 recalls naming Indiana we have scored against our rubric, 1,908 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,536 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,598 recalls whose distribution notice names Indiana specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Specialized is recalling about 1,800 Fuse Comp and Fatboy SE bicycles with Stout cranks because the driveside crankarm can disengage, posing fall and injury hazards.
Cook Inc. is recalling 751 units of the StoneBreaker Pneumatic Lithotripter because the device may not be properly sterilized during reprocessing.
Radiometer Medical ApS is recalling AQURE software versions 2.3.0 and 2.3.1 due to a potential problem that may result in patient mix-up.
Cook Inc. is recalling 12,556 StoneBreaker Single Use Probes because the interior may not be properly sterilized. The recall covers units distributed in the US and 70 other countries.
Zimmer Biomet is recalling 30 modular hip head components because two lots of different sizes were potentially commingled. This error could lead to the use of an incorrect sized head, causing surgery delays or dislocation.
Cook Inc. is recalling 470 StoneBreaker Sterilization Caps because the interior may not reach the required Sterility Assurance Level during reprocessing.
Siemens Medical Solutions is recalling 42 Biograph Horizon PET/CT scanners due to a software error that causes incorrect image reconstruction.
Roche Diagnostics is recalling cobas b 221 AutoQC Modules because a software defect prevents the scheduled quality control measurements from starting.
Roche Diagnostics is recalling 1,026 Omni S2 analyzers because a software defect prevents scheduled quality control measurements from starting.
Rhodes Pharmaceuticals is recalling Aptensio XR capsules because they failed to meet dissolution specifications. The affected lot was distributed nationwide.
Roche Diagnostics is recalling 1,026 OMNI S4 analyzers because a software defect prevents the AutoQC scheduler from activating.
CooperSurgical, Inc. is recalling 520 units of 5 mm Apple-Hunt Secondary Cannulas because they were packaged with the wrong trocar length type.
Roche Diagnostics is recalling 1,026 OMNI S6 analyzers because a software defect prevents scheduled AutoQC measurements from starting.
Philips is recalling 682 Allura Xper and UNIZ interventional fluoroscopic x-ray systems because the large screen monitor may freeze for 15 seconds after continuous operation.
IntroMedic Co., Ltd. is recalling 82 units of the Miriam Capsule Endoscope System because the battery indicator may incorrectly display orange when the battery is fully charged.
Hauck is recalling Nerf Battle Racer go-karts because the steering wheel can detach, break, or crack, posing laceration and collision risks to children.
Daimler Trucks North America is recalling 2002-2018 Thomas Built Buses Minotour school buses with wheelchair lifts due to a wiring defect that allows the lift to operate while the vehicle is in motion.
Daimler Trucks North America is recalling 2018-2019 Freightliner Cascadia vehicles because driver's air bag fasteners may not be installed correctly, potentially affecting deployment.
Nova Bus is recalling 2015-2017 LFS and LFS Artic transit buses because a brake guide pin may break, potentially causing loss of braking ability or tire pressure.
Forest River is recalling 2018 Surveyor recreational trailers because a missing fan in the slide-out refrigerator may cause overheating and increase the risk of a fire.
Entegra is recalling 2019 Vision and Emblem motorhomes because the windshield wiper motor may fail in heavy snow or ice, reducing driver visibility.
Jayco is recalling 2018-2019 Precept and 2018 Alante vehicles because the windshield wiper motor may fail in heavy snow or ice, reducing driver visibility.
General Motors is recalling 2014-2017 Chevrolet Express and GMC Savana vans because liquid leakage in the driver's window switch can cause corrosion and increase the risk of a fire.
Porsche is recalling 2015 918 Spyder vehicles because rear suspension connecting shafts may fail due to stress corrosion cracking, increasing the risk of a crash.
Navistar is recalling 2018-2019 International trucks and buses because the front seat belt anchor bolt may break in a crash, increasing injury risk.