State
73,219 recalls have nationwide distribution and so reach Indiana. 9,587 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,587 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 2,149 (22%) are Severe.
Which agencies issued them
These figures cover only the 9,587 recalls whose distribution notice names Indiana specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
AVKARE LLC is recalling Tranexamic Acid USP 650mg tablets nationwide due to failed quality control specifications for conductivity. No illnesses have been reported.
Tesla is recalling 26 Model 3 and Model Y vehicles from 2023 because the pyrotechnic battery disconnect may fail to isolate the high-voltage battery after a crash, creating a risk of electrical shock.
Altec is recalling 1999-2022 L and LR Series aerial devices because a hydraulic hose may fail, causing the platform or load to move unexpectedly.
Honda recalls 2023 Civic vehicles with a defective brake modulator that may leak fluid, potentially causing unintended vehicle movement or increased brake pedal travel.
Mazda is recalling 2024 CX-90 vehicles because steering and suspension bolts may be missing or improperly tightened, posing a risk of loss of vehicle control.
Huish Outdoors is recalling Oceanic brand SCUBA diving buoyancy compensating devices because the weight pocket handle can break during use, preventing divers from dumping weight in an emergency to surface safely. No injuries have been reported, but 73 broken handles have been documented.
A faulty MOST cable connector in certain 2018-2023 Honda Odyssey, Pilot, and Passport vehicles may prevent the rearview camera image from displaying, reducing rear visibility and increasing crash risk.
Toyota is recalling 298 2023 Camry and Camry Hybrid vehicles because lug nuts attaching wheels may be loose, risking wheel detachment and loss of vehicle control. Owners are advised not to drive until dealers repair the issue.
Grand Design RV is recalling certain 2023 Momentum toy haulers due to an incorrect Cargo Carrying Capacity label. The mislabeled weight information can lead to vehicle overload, increasing crash risk.
Trek Bicycle Corp. is recalling about 96,900 bicycles equipped with Promax hydraulic disc brakes because the brake hose can detach from the brake lever, posing a crash hazard. Trek has received 195 reports of this issue with no injuries reported.
Johnsonville is recalling approximately 42,062 pounds of Beddar with Cheddar pork sausage links due to possible contamination with thin black plastic fibers.
Environmental debris accumulation may block flow sensors in Philips ventilators, potentially preventing accurate pressure and flow delivery to patients.
BearCare's Walnut Wearable Smart Thermometer (Model WT20) is being recalled due to reports of skin burns in children ages 0-6. The device was distributed nationwide; 1818 units were affected.
Philips Respironics recalled approximately 57,395 ventilators due to environmental debris potentially accumulating on the flow sensor, which may prevent accurate delivery of pressure and volume to patients, risking hypoxemia.
A software anomaly in StealthStation Cranial Software causes depth gauge displays to lose synchronization during cranial biopsy procedures, risking inaccurate surgical guidance and tissue injury.
Philips Respironics recalled 18,855 Trilogy Evo O2 EV300 devices because environmental debris may accumulate on the flow sensor, potentially causing inaccurate delivery of pressure or flow. This could result in patient hypoxemia if not promptly addressed.
Great Dane is recalling 2024 Champion and Everest trailers because tire pressure may drop at speeds over 45 mph, increasing crash risk.
Meijer Inc is recalling Frederik's by Meijer Dark Chocolate Almonds due to undeclared milk. The product was distributed to Meijer stores in six Midwest states.
Stoughton Trailers is recalling 2023-2024 Intermodal container chassis because improperly tightened wheel lug nuts can allow the wheel to detach, increasing crash risk.
The FDA has issued a Class I recall for the Trilogy Evo Universal Ventilator Model DS2000X11B, affecting 22,237 units distributed nationwide and globally. The device is manufactured by Philips Respironics, Inc.
Meijer Inc is recalling Meijer Express Dark Chocolate Covered Almonds due to undeclared milk, a serious risk for consumers with milk allergies. The recall affects 9,030 units in Michigan, Indiana, Illinois, Ohio, Kentucky, and Wisconsin.
Golden State Medical Supply is recalling Travoprost eye drops due to missing tamper evidence seals on some bottles. The missing seal prevents sterility assurance on 1,920 units distributed nationwide.
Avanos Medical is recalling SMMT ambIT Reusable cassettes (Product Code 220568, Lot 30191805) that were potentially distributed without a required air-in-line filter. The missing component affects units in Texas, Oregon, and Australia.
BioReference Health is recalling the 4Kscore Test system due to software anomalies in its processing module that may generate erroneous diagnostic results. The recall affects 662 patient test results distributed in New Jersey.
Qiagen Sciences LLC recalls 347 QIAstat-Dx Respiratory SARS-CoV-2 test kits due to faulty cartridges that could produce false results. Affected kits were distributed nationwide in nine states.