State
73,566 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, 1,913 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,529 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,592 recalls whose distribution notice names Indiana specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
LoHi Tech is recalling about 24,900 SOWTECH Espresso Machines (Model CM6811) because the glass carafe can break during use, posing a burn hazard. The firm has received 48 reports of breaking carafes, resulting in five burn injuries.
BMW is recalling one 2019 X5 xDrive 40i because a manufacturing defect in the instrument panel may prevent the passenger air bag from deploying properly in a crash.
BMW is recalling 2018-2019 X3 and X4 vehicles because the front passenger air bag may fail to deploy due to a sensor assembly error.
Maintainer is recalling 2019-2020 Service/Mechanics Bodies mounted on International MV607 vehicles because crane mounting bolts are too short to securely attach the crane.
Thor Motor Coach is recalling multiple RV models due to defective adhesive bonding in Hehr 6400 series windows. The vented portion may detach, increasing risk of crash or injury.
General Motors is recalling certain 2022 Chevrolet Bolt EV and Bolt EUV vehicles because driver-side air bag fasteners may be missing or improperly tightened. This could prevent the air bag from deploying properly in a crash.
Kia is recalling 2022 K5 vehicles with 2.5L turbocharged engines due to fuel leaks that increase fire risk. Dealers will repair the fuel pipe at no cost.
Canyon Furniture has recalled about 1,200 Creekside Kids Five-Drawer Chests sold at Rooms To Go because the chests are unstable without wall anchoring and pose tip-over and entrapment hazards to children.
ECHO EGi-2300 Watt Generators can overheat and catch fire, posing a fire and burn hazard. The manufacturer has received four reports of overheating or fire, though no injuries have been reported.
Premium OrgaZEN 7000 capsules distributed nationwide have been recalled because they were marketed without FDA approval and contain undeclared sildenafil and/or tadalafil, prescription drugs that pose serious health risks.
NSNY Distributor Inc is recalling Ginseng Power 5000 capsules nationwide because they contain undeclared sildenafil and/or tadalafil, prescription medications not listed on the label or approved for sale in this product.
The LeadCare II Blood Lead Test Kit may generate artificially low control test results, causing blood lead levels to be underestimated in patient samples. Kits were distributed worldwide.
ProtectoRx hand sanitizer (ethyl alcohol 70%) is being recalled nationwide because some lots were found to contain methanol and all lots were manufactured under the same conditions as the contaminated product.
DiBAR LABS Hand Sanitizer (70% ethyl alcohol) in 16 FL OZ and 8 FL OZ bottles is being recalled nationwide because other lots and products made under the same conditions were found to contain methanol.
Dibar Labs is recalling Advance Hand Sanitizer (70% ethyl alcohol, 16 FL OZ) distributed nationwide because it was manufactured under the same conditions as lots found to contain methanol.
Magellan Diagnostics recalls LeadCare Plus Blood Lead Test Kit after control tests generated low results, potentially underestimating patient blood lead levels. Affected lot numbers include 2011MU, 2104MU, and 2108MU.
Altec is recalling 2020-2021 D2000, D3000, and D4000 Derrick diggers because an improperly seated retaining ring allows the boom to rotate unintentionally, increasing injury risk.
DiBAR LABS Hand Sanitizer (ethyl alcohol 70%, 8 FL OZ) is being recalled because FDA testing found three lots contain methanol contamination and have ethanol content below the label claim.
Quidel Corporation is recalling approximately 29,787 kits of the Lyra SARS-CoV-2 Assay due to a theoretical risk that samples with very high viral loads could produce false negative results. No false negatives have been formally reported.
Xtreme Outdoors is recalling 2021 MyPod travel trailers because a support bracket may be insufficient, potentially causing the trailer shell to detach and create a road hazard.
Magellan Diagnostics is recalling the LeadCare Ultra Blood Lead Test Kit due to control test failures causing potential underestimation of blood lead levels in patient samples. The recall involves 441 kits with worldwide distribution.
Daimler Vans USA is recalling 2021 Mercedes-Benz Sprinter, Metris, and Freightliner Sprinter vehicles because seat belt retractors may deactivate early, preventing child restraints from securing properly.
One lot of PORTEX ULTRperc Percutaneous Dilation Tracheostomy Kit (Lot 4072715) was incorrectly labeled as 7.0mm when it is 9.0mm. The 40 units were distributed in Pennsylvania, Michigan, Maryland, and Florida.
Philips is recalling 1,301 monitor bracket assemblies used with CT systems due to shaft wear that could cause monitors to fall, potentially injuring patients, operators, bystanders, or service personnel.
Philips CT fluoroscopy monitors may develop bracket shaft wear that could lead to the monitor detaching and falling while attached to cables.