State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Chrysler is recalling 2017 Jeep Compass vehicles because the User's Guide contains reversed battery terminal polarity for jump starting, which may increase the risk of injury.
Forest River is recalling specific 2015-2018 transit buses and work trucks because a flexible coupling may fail, potentially damaging brake and fuel lines.
Ford is recalling 2017 Edge, Fusion, and Lincoln MKZ vehicles with 2.0L engines and six-speed automatics because torque converter weld studs may be inadequate, risking loss of vehicle movement.
Cub Cadet is recalling approximately 4,000 2016 Challenger utility vehicles because air in the brake system can cause brake failure, posing a crash hazard.
BMW is recalling 2006 3 and 5 Series vehicles because the front passenger seat occupant detection mat may crack, potentially deactivating the air bag in a crash.
Cummins is recalling L9 heavy-duty diesel engines installed in Pierce fire trucks because improperly tightened capscrews may cause the flexplate to separate, potentially leading to engine stalling and a crash.
Home Depot is recalling Hampton Bay and Home Decorators Collection crystal chandeliers because halogen bulbs can melt parts, posing fire and burn risks.
DeRoyal Industries is recalling 426 Dolphin Inflation Devices due to a primary packaging defect that may compromise sterility.
Allergan is recalling 648 units of Blephamide ophthalmic ointment because stability testing showed impurities exceeding specifications.
The Kroger Co is recalling Dessert Cups yellow sponge cakes because the packaging fails to list milk in the allergen statement, despite it being an ingredient.
Olympus Corporation of the Americas is recalling 1,264 High Frequency Resection Electrodes because loop wires may break at the distal end.
Shimadzu Medical Systems is recalling ceiling-type X-ray tube supports because cracks may develop on the tube holding shaft, posing a risk of equipment failure.
Merge Healthcare is recalling 219 SpO2 connecting cables for its Hemodynamics monitors because they may stop displaying patient SpO2 readings, causing a slight delay in patient care.
Carestream Health Inc is recalling DRX-Revolution Mobile X-Ray Systems because missing screws could cause the tube and yoke assembly to separate.
Mindray is recalling 2,718 TI Transport Monitor battery packs because two reports indicated the packs overheated.
Merge Healthcare is recalling specific versions of its LIS software because wrong laboratory results could be inadvertently verified under certain conditions.
Elekta is recalling MOSAIQ Oncology Information System versions 2.50.05 and higher because outdated information may remain in order sets, potentially affecting treatment workflows.
Intuitive Surgical is recalling 10 da Vinci Xi Surgical Systems because brake screws on the patient side carts may be under-torqued.
Shimadzu is recalling RADspeed Pro stationary x-ray systems because cracks may develop on the tube holding shaft, posing a risk of equipment failure.
Merge Healthcare is recalling four MasimoSET pediatric SpO2 sensors because cables may stop displaying patient data, causing slight delays in care.
Covidien LLC is recalling 194,851 units of the Endo Peanut 5mm Auto Suture Blunt Dissector because the cotton tip may disengage due to insufficient adhesive.
Shimadzu is recalling FDR Visionary x-ray systems because cracks may develop on the tube holding shaft. The recall covers 1,673 units distributed in the US, Canada, and Japan.
Merge Healthcare is recalling 65 MasimoSET LNOP DCI adult SpO2 reusable sensors because cables may stop displaying patient SpO2, causing slight delays in care.
AGFA Healthcare Corp. is recalling 10 units of IMPAX Cardiovascular software because it displayed incorrect aneurysm findings in NIV reports.
American Pharmaceutical Ingredients LLC is recalling Doxycycline Hyclate USP active pharmaceutical ingredient due to misbranding. The product is subject to FDA Import Alert 66-66.