State
73,584 recalls have nationwide distribution and so reach Indiana. 9,592 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,592 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 2,534 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,592 recalls whose distribution notice names Indiana specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
MTIG Productions is recalling deSensua Wintergreen, Birch, and Pain Soother Essential Oils because the packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.
Daimler Trucks North America is recalling 2019-2020 Freightliner Custom Chassis XBA vehicles due to engine software that may fail to limit speed or torque, increasing crash risk.
Liq-E S.A. De C.V. is recalling Optimus Lubricants Instant Hand Sanitizer because the product contains methanol and has lower ethanol content than labeled.
Liq-E S.A. De C.V. is recalling Optimus Lubricants Instant Hand Sanitizer because the product contains methanol and has lower ethanol content than labeled.
Liq-E S.A. De C.V. is recalling Optimus Lubricants Instant Hand Sanitizer because the product contains methanol and has lower ethanol content than labeled.
Liq-E S.A. De C.V. is recalling 575 drums of Optimus Instant Hand Sanitizer because the product contains methanol and has lower ethanol content than labeled.
Combat Medical Systems is recalling 954 Fresh Whole Blood Donor Sets due to a potential bent or disconnected needle in the kit components.
Lamborghini is recalling 2018-2021 Aventador SVJ vehicles because hood hinge screws may loosen, potentially causing the hood to detach at high speeds.
Combat Medical Systems is recalling Fresh Whole Blood Transfusion Sets due to a potential for bent or disconnected needles in the kit components.
Combat Medical Systems, LLC is recalling 1021 units of Low Titer Type O FWB Transfusion Sets due to the potential for bent or disconnected needles in the components.
Combat Medical Systems is recalling 531 Valkyrie LTOWB blood collection kits due to a potential for bent or disconnected needles.
Combat Medical Systems is recalling 953 Valkyrie LTOWB Administration Sets due to a potential for bent or disconnected needles.
Certain 2021 International LT vehicles with Cummins X15 engines may have improperly torqued flywheel capscrews that could detach during operation, causing loss of drive power and risk of ejected engine parts.
Becton Dickinson is recalling 155,200 10 ml syringes because open packaging seals may compromise sterility. The product was distributed in the US and Canada.
SmartPool is recalling Bee Free children's helmets because they do not meet safety standards for children under 5, posing a risk of head injury.
Confirm Biosciences is recalling Orient Gene COVID-19 Rapid Test Cassettes because they were distributed outside Emergency Use Authorization and not validated for fingerstick use.
Volvo is recalling 2021-2022 XC40 Recharge vehicles because a battery software defect may cause the high-voltage system to disconnect, increasing crash risk.
Urban Outfitters is recalling Margo Taper Candle Holders because they can catch fire if they contact the flame. One fire incident was reported, with no injuries.
Getinge is recalling CM320 Series Washer Disinfectors because plastic inlet hose connections may deform or break, potentially causing water leaks and burns.
Biomet is recalling 49 units of 25mm central screws for shoulder prostheses because they were mislabeled as 25mm but are actually 40mm.
Polestar is recalling certain 2021-2022 Polestar 2 vehicles. A software issue in the Battery Energy Control Module may cause the high voltage system to disconnect, resulting in loss of drive power and increased crash risk.
Carl Zeiss Meditec is recalling 613 IOLMaster 700 devices because software versions 1.90.2.09 and 1.90.8.06 may display incorrect patient information when using the modality worklist.
Northern Tool & Equipment is recalling Powerhorse 13000ES portable generators due to a wiring error that can cause electrical shock. No injuries have been reported.
GE Healthcare is recalling 96 Revolution CT systems because a damaged or missing table pinch protector may expose sharp screws, posing a laceration risk.
GE Healthcare is recalling Revolution CT and Revolution CT ES systems because damaged or missing table pinch protectors may expose sharp screws, posing a laceration risk.