State
73,190 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 73,190 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
GlaxoSmithKline is recalling TUMS Antacid tablets (Lot HB2G) due to glass mineral wool contamination. Affected product was distributed nationwide.
Cepheid is recalling 1,413 Xpert Xpress Strep A test kits due to a defect in the included pipettes. Defective pipettes may fail to dispense adequate sample volume, resulting in invalid test results or no test result.
Edenbridge Pharmaceuticals recalled opium tincture nationwide because the morphine concentration fell below labeled potency. The voluntary recall affected 4,548 bottles.
Glenmark Pharmaceuticals is recalling Bisoprolol Fumarate and Hydrochlorothiazide Tablets due to failed impurities and degradation specifications. The recall affects 480 bottles distributed nationwide.
Hillrom Progressa+ hospital beds (499 units) are being recalled due to potential static electricity buildup that could cause mild shock to operators during transport. The affected units were distributed nationwide.
Coapt LLC is recalling 109 ControlSeal Electrodes due to risk of minor burns or blistering if exposed to direct sunlight or warm temperatures exceeding 12 hours, or if the battery is damaged.
Vasoview 6 Pro endoscopic vessel harvesting systems were packaged in incorrect outer boxes displaying artwork for a different device (Vasoview Hemopro 2). The inner labels and product documentation are correct.
Smiths Medical recalls a pediatric tracheostomy tube because the outer box shows an incorrect expiration date (3/17/2021) while the actual product has the correct date (3/17/2026). The discrepancy could cause confusion about product validity.
Safecor Health recalls Strong Iodine Solution nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The prescription product was distributed in multiple lots across the U.S.
Alexis Fire Equipment is recalling 2021-2024 Fire Apparatus vehicles because a defect in the inversion valve may delay parking brake engagement, increasing the risk of unintentional vehicle movement.
Mack Trucks is recalling 2024 MD trucks because the steering wheel attachment bolt may loosen and separate, potentially causing the steering wheel to detach.
Cruise LLC is recalling 950 vehicles because a software defect in the Collision Detection Subsystem may cause the vehicle to move after a crash.
Custom Fire Apparatus is recalling 2021-2024 Spartan emergency vehicles because a parking brake defect may allow unintentional movement, increasing crash risk.
PACCAR is recalling 2024 Peterbilt 520 vehicles because a rear lifting bracket may detach, posing an injury risk during engine lifting.
General Motors recalls certain 2024 Buick Envista vehicles for a software defect that may cause the instrument panel display to go blank, preventing visibility of critical safety information like vehicle speed and warning lights.
Winnebago is recalling 2017-2018 Micro Minnie travel trailers because the murphy bed may raise unintentionally, posing a risk of trapping occupants.
Evenflo is recalling one Titan 65 child seat because it is missing required warning labels, which may increase the risk of injury to the occupant.
Gillig is recalling 2019-2023 Low Floor transit buses because the transmission yoke may separate, causing a sudden loss of drive power and increasing crash risk.
Mercedes-Benz is recalling 2024 GLC 300 vehicles because windows may detach and airbags may lack proper support, increasing crash and injury risks.
Tesla is recalling 2021-2024 Model S and Model X vehicles because an incorrect air bag was installed when the steering wheel was replaced. The incompatible air bag could deploy incorrectly during a crash, increasing the risk of injury.
Forest River is recalling 2023-2024 Sandstorm, Stealth, and 2024 Shockwave travel trailers. The electrical wire from the 50-amp inlet has incorrect gauge and may melt, creating a fire hazard.
Forest River is recalling certain 2018-2024 Coachmen Adrenaline and 2020-2024 Work and Play fifth wheels and travel trailers because side marker lights may not reflect light properly, reducing visibility to other drivers and increasing crash risk.
Gulf Stream is recalling 2024 travel trailers because incorrect tire size and pressure information on the Federal certification label may lead to overinflation and loss of vehicle control.
Fairmont Foods is recalling approximately 147,132 pounds of frozen spaghetti loops with meat sauce due to misbranding and an undeclared egg allergen.
Autocar is recalling 2023 Legend and Xpeditor vehicles because wheel lug nuts may not be tightened properly, increasing the risk of a crash.