State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Philips is recalling Ingenuity Core128 CT scanners due to software issues in versions 4.1.3, 4.1.4, and 4.1.5 that could affect equipment performance.
Philips is recalling five Ingenuity Core 128 CT systems due to a software defect causing intermittently slow response of the Host.
Philips is recalling 899 MX 16-slice CT systems due to software defects that may cause patient image mix-ups or scan interruptions.
Siemens is recalling AXIOM Artis angiography systems because biomass contaminants in the cooling system may damage the pump.
Invacare is recalling 395 Precise Rx Pediatric Flowmeters because the rear gradation scale was printed upside down, which may cause confusion during oxygen flow monitoring.
Nutritional Resources Inc. is recalling Healthwise Protein Chips because foreign plastic was observed in the product.
Topcon Medical Laser Systems is recalling 205 PASCAL Synthesis ophthalmic laser systems worldwide due to a software anomaly affecting the titration process when specific functions are used.
Philips Medical Systems is recalling 318 Brilliance 64 Computed Tomography X-ray systems due to a software defect causing intermittently slow response of the Host.
Philips Medical Systems is recalling 29 Ingenuity Core CT systems due to a software defect causing intermittently slow response of the Host.
Siemens Medical Solutions is recalling Artis Q and Q.Zen angiography systems because biomass in the cooling system may damage the pump.
Nobel Biocare is recalling 231 Guided Surgery Kits because the Instructions for Use contain an incorrect drill protocol. The kits are used for NobelParallel CC Implants.
Invacare is recalling 395 Precise Rx Pediatric Flowmeters because the rear gradation scale was printed upside down, which may confuse users.
Philips Medical Systems is recalling 335 Brilliance iCT units due to software issues in versions v4.1.3 and v4.1.5 that could affect equipment performance.
Siemens is recalling AXIOM Artis angiography systems because biomass contamination in the cooling system may damage the pump.
Philips Medical Systems is recalling 203 Brilliance 16 CT systems due to a software defect causing intermittently slow response of the Host.
Philips Medical Systems is recalling 55 Brilliance CT 16 Power systems due to a software defect causing intermittently slow response of the Host.
Becton, Dickinson and Company is recalling 14,089 vials of BD Tritest CD3 FITC/CD4 PE/CD45 PerCP because the label incorrectly states the product contains gelatin.
C.R. Bard is recalling 64 Medivance ArcticGel Neonatal Pads because the included instructions were missing required languages for CE-marked products.
Sauder Woodworking is recalling about 8,000 Storybook four-drawer chests sold at Walmart.com due to a serious tip-over hazard that could injure children.
Kovatch Mobile Equipment is recalling 27 KME Predator emergency vehicles from 2012-2013 because the front grille may loosen and separate from the cab, creating a road hazard.
Mercedes-Benz is recalling 2016 C300 and GLC300 vehicles because a damaged Electronic Stability Program control unit may activate stability control or disable the parking brake, increasing crash risk.
Autocar is recalling 294 model year 2016-2017 Xspotter vehicles because a steering column shaft weld may break, causing a loss of steering ability and increasing crash risk.
Spartan Motors is recalling 2014-2016 Legend and Star fire trucks due to a transmission defect that may prevent power output switching, risking injury.
Keystone is recalling 2011-2017 Bullet and Passport recreational trailers because an improperly wired air conditioner thermostat may cause an electrical short and fire.
Mercedes-Benz is recalling 2016 GLE450 vehicles because rear head restraints may not stay locked in very low temperatures, increasing injury risk in a crash.