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.
Siemens is recalling 73 Artis zee ceiling units because the display may fail to show images after power save mode, potentially requiring procedure cancellation.
Siemens is recalling Artis Q.zen floor units because the display may fail to show images after power save mode, potentially requiring procedure cancellation or patient transfer.
Siemens is recalling four Artis Q.zeego X-ray systems because the display may remain black after power save mode, preventing normal operation and requiring procedure cancellation or patient transfer.
St Jude Medical is releasing new firmware for Merlin PCS programmers to strengthen security against unauthorized access to cardiac devices.
Siemens is recalling five Artis Q biplanes because the display may fail to show an image after power save mode, potentially requiring procedure cancellation or patient transfer.
Toshiba is recalling 162 Aplio I-series diagnostic ultrasound systems because the power supply unit may be damaged and fail to start up.
Siemens is recalling two Artis zee biplane MN systems because the large display may fail to show an image after power save mode, potentially requiring procedure cancellation or patient transfer.
Randox Laboratories is recalling Liquid Assayed Specific Protein Control - Level 2 because Free Kappa light chains increase over shelf life, potentially delaying diagnostic results.
Horiba Medical is recalling ABX Pentra Micro Albumin 2 CP reagents because they may produce elevated results if used immediately after a specific creatinine reagent.
St Jude Medical is recalling Ellipse ICDs and CRT-Ds to release new firmware that strengthens security against unauthorized access.
Randox Laboratories is recalling Liquid Assayed Specific Protein Control Level 1 because Free Kappa light chains increase over shelf life, potentially delaying diagnostic results.
St Jude Medical is recalling Fortify Assura implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
St Jude Medical is recalling Unify ICDs and CRT-Ds to release new firmware that strengthens security against unauthorized access.
Absonutrix is recalling Lyfetrition Vitamin B12 supplements because the product did not contain the vitamin listed on the label.
Forest River and Coachmen are recalling specific RV models because liquid leaks into the driver's power window switch, causing corrosion and increasing the risk of a fire.
Lippert Components is recalling Solera Smart Arm Awnings because water intrusion may cause them to deploy while driving, increasing crash risk.
Nueske's Meat Products is recalling approximately 12,946 pounds of braised pork products because they may contain undeclared brown rice flour and glycerin.
Daimler Trucks North America is recalling 2015-2018 Freightliner Custom Chassis Corporation XCL chassis with V-Ride suspension because mounting bolts may loosen, affecting vehicle stability.
Spartan Motors is recalling 2010-2019 Gladiator vehicles because a brittle battery cable sleeve can cause chafing and arcing, increasing the risk of a fire.
BRP is recalling about 13,300 2018 Can-Am Outlander and Renegade ATVs because fuel can spray from the tank when opening the gas cap, posing a fire hazard.
Helmets R Us is recalling about 9,700 Rollerblade helmets sold to schools because they fail to meet federal safety standards, posing a risk of head injury.
Suzuki is recalling 2018 DR-Z400S and DR-Z400SM motorcycles because resin may prevent the rear brake light from illuminating, increasing crash risk.
Turn5, Inc. is recalling specific Mammoth-brand wheels that may develop cracks, potentially leading to wheel failure and loss of vehicle control.
BMW is recalling 2018 X5 and X6 vehicles because a front lower-left control arm pivot bolt may not be properly hardened, potentially causing the arm to break and increasing crash risk.
General Motors is recalling 2016-2018 Cadillac CT6 vehicles because excess adhesive on child seat anchorage bars may interfere with proper installation, increasing injury risk.