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.
Tesla is recalling 2,676 Model X vehicles because the third row seat back may move forward in a crash, increasing injury risk.
Nipoamerican is recalling specific Elegance and Evolution mattresses because they fail to meet federal open flame standards. Consumers should contact the company for free protective covers.
Siemens is recalling 124 SOMATOM Emotion and Sensation CT systems due to a potential malfunction hazard when using specific cardio licenses.
Siemens is recalling 552 Artis zeego angiography systems due to risks of mechanical cable damage and high-voltage generator module failure.
Mitsubishi Heavy Industries is recalling VERO MHI-TM2000 Linear Accelerators because the operator console may set an incorrect gantry angle for the first beam of an IMRT treatment.
Terumo is recalling 222 CDI Blood Parameter Monitoring System 500 devices because a faulty thermistor may cause inaccurate temperature and analyte readings.
Roche Diagnostics is recalling the Elecsys Estradiol II assay because fulvestrant treatment causes falsely elevated estradiol results.
Siemens is recalling 124 CT systems due to a potential malfunction hazard when using specific cardio licenses.
Siemens is recalling 124 SOMATOM Emotion and Sensation CT systems due to a potential malfunction hazard when using specific cardio licenses.
Siemens is recalling 124 CT systems due to a potential malfunction hazard when using specific cardio licenses.
Ossur Americas is recalling Papoose Infant Spine Immobilizers and other orthopedic devices due to a defect described as 'the p'.
Ossur Americas is recalling various orthopedic braces and medical devices due to unspecified product defects.
Ventura Foods is recalling 35 lb. jugs of cooking oil because plastic fragments may be present due to a manufacturing defect in the jugs.
Siemens is recalling 986 AXIOM Artis zee/zeego angiography systems because a cooling system leak could cause equipment failure.
GBG Accessories Group is recalling Ivanka Trump-branded scarves because they do not meet federal flammability standards, posing a burn risk.
Ossur Americas is recalling various medical devices, including knee undersleeves and walkers, due to a defect described in the source text.
Key Safety Systems is recalling specific driver frontal air bags that may deploy improperly due to a missing chemical enhancer, increasing injury risk.
Maquet is recalling Cardiosave Hybrid and Rescue IABP devices because the scroll compressor may not meet specifications for output pressure or vacuum at specific flow rates.
Roche is recalling the Estradiol III assay because fulvestrant treatment causes falsely elevated estradiol results, potentially leading to incorrect patient management.
Ossur Americas is recalling Rebound Diabetic Walkers and other medical devices due to a defect described as 'the p'.
Synthes (USA) Products LLC is voluntarily recalling 42 lots of 4.5 mm LCP Proximal Tibia Plate Systems due to a medical device defect.
Ossur Americas is recalling various medical devices, including knee braces and walkers, due to unspecified product issues.
Ossur Americas is recalling NecLoc Extrication Collars and other medical devices due to a defect described as 'the p'.
Siemens is recalling 124 CT systems due to a potential malfunction hazard when using specific cardio licenses.
Hale Products Inc. is recalling portable pumps with Yanmar diesel engines due to a mislabeled dashboard warning light that could hinder fire suppression.