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.
Rena Ware is recalling about 700 Nutrex pressure cookers because they can discharge steam at lower pressures than intended, posing a burn hazard.
Zebra Technologies is expanding a recall of power supply units for thermal printers due to a fire hazard. The units can overheat and catch fire when exposed to moisture.
Dexter Axle Company is recalling certain trailer axles because incorrect tapered roller bearings may have been installed, increasing the risk of a crash.
Newmar is recalling 119 motorhomes because brake caliper mounting bolts may be insufficiently tightened, potentially reducing braking performance and increasing crash risk.
Subaru is recalling 2019 Ascent vehicles because missing spot welds on the B-Pillar may compromise vehicle strength, increasing the risk of injury in a crash.
Thor Motor Coach is recalling 2017-2019 Aria and Venetian motorhomes because brake caliper mounting bolts may loosen, potentially reducing braking performance.
Miller Fireworks is recalling specific rocket and cracker fireworks that violate federal standards due to explosion and burn hazards.
General Motors is recalling 2018 Chevrolet Express and GMC Savana vans because the tire pressure monitoring system may be incorrectly calibrated, potentially delaying low-pressure warnings.
CPSC recalls Hill Topper electric bike motor controllers that may accelerate on their own, posing crash and injury risks to riders.
Textron Specialized Vehicles is recalling about 255 Arctic Cat snowmobiles because the handgrip can break, posing an injury hazard to the rider.
Major Pharmaceuticals is recalling specific lots of 80 mg Valsartan tablets because a carcinogen impurity was detected in the active ingredient.
Olympus is recalling 2,399 Uretero-reno fiberscopes because the insertion tube bending section may break during surgery.
Major Pharmaceuticals is recalling specific lots of 160 mg Valsartan tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Cayenne Medical Inc. is recalling specific models of the AperFix Femoral Implant Coring Removal Drill due to a trend of premature wear and breakage identified in 2010.
Philips Healthcare is recalling 459 Allura Xper systems because shutter positions reset when procedure types change, potentially affecting imaging accuracy.
Olympus is recalling 2,548 Uretero-reno videoscopes because the insertion tube bending section may break during surgery.
Ad-Tech Medical Instrument Corporation is recalling 65 Drill Sleeve Guides because raw material diameter was under tolerance, which could cause drill bits to seize during surgery.
BMC is recalling about 430 Timemachine 01 bicycles because insufficient space between the front wheel and downtube poses a fall hazard. Four fall incidents were reported, including one broken finger.
H&H Sports Protection is recalling VCAN V531 motorcycle helmets because the straps may not be properly sewn, potentially failing to stay secured during a crash.
Elekta, Inc. is recalling 725 HexaPOD evo RT Couch Top devices because they may tilt incorrectly after specific workflows, leading to improper patient positioning during radiation therapy.
Tactical Medical Solutions is recalling 1,097 units of BLAST Bandages, Lot 0617, because they were not terminally sterilized.
GE Medical Systems is recalling 54 MR Surgical Suite Option units because a defect in the table transfer release may cause an unexpected loss of function in the patient transfer mechanism.
Sun Pharmaceutical Industries is recalling Testosterone Cypionate Injection vials because organic and inorganic particulate matter was detected in the product.
Olympus is recalling 1,062 Uretero-reno fiberscopes URF-P6 because the insertion tube bending section may break during surgery.
Bard Medical Division is recalling 5,608 Arctic Sun 5000 Temperature Management Systems because an improper wiring connection may cause overheating and component failure.