State
73,491 recalls have nationwide distribution and so reach Indiana. 9,589 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,589 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 2,528 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,589 recalls whose distribution notice names Indiana specifically. The 73,491 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Fresh Express Inc is recalling Leafy Romaine salad in 9oz. and 10oz. packages due to potential Listeria monocytogenes contamination. The product was distributed to multiple states and Canada.
Fresh Express Inc is recalling Old Fashion Coleslaw (14oz packages) due to potential Listeria monocytogenes contamination across 20 U.S. states and Canada.
Fresh Express Inc is recalling Asian Avocado salad products in 9.7oz packages due to potential contamination with Listeria monocytogenes. The recall affects approximately 1,053 cases distributed across multiple U.S. states and Canada.
Fresh Express Inc is recalling approximately 98,358 cases of "Sweet Butter" salad in 6oz. packages due to potential Listeria monocytogenes contamination. The product was distributed to retailers in 20 U.S. states and Canada.
Edge Pharma is recalling a sterile ophthalmic solution due to lack of assurance of sterility. The recall affects 2,562 syringes distributed nationwide.
D&D Technologies is recalling about 1,500 SureClose READYFIT 180° hinge-closer sets because they can malfunction and fail to fully self-close gates, allowing unintended access to pools and posing injury and drowning hazards to young children.
Velano Vascular is recalling 123,700 PIVO Blood Collection Device 20G units due to incomplete package sealing that could compromise sterile barriers and allow microbial contamination.
Edge Pharma is recalling Ceftazidime sterile ophthalmic solution for intraocular injection due to lack of assurance of sterility. The recall affects 168 syringes distributed nationwide.
BAOPTEIL-branded children's robes sold on Amazon fail to meet federal flammability standards for children's sleepwear, posing a burn hazard. About 3,800 units sold from December 2019 through August 2021 are affected.
Edge Pharma, LLC is recalling Methacholine Challenge 5-Syringe Test Kits nationwide due to lack of assurance of sterility. The sterile inhalation solution may not meet sterility standards.
Porsche is recalling one 2021 Taycan with misaligned front and rear suspension. The misalignment may cause uneven tire wear and increase crash risk.
Siemens is recalling 23 Artis icono angiography systems due to four software defects that could disable imaging, corrupt images, and cause unexpected shutdowns during patient procedures.
Siemens is recalling its Artis pheno diagnostic angiography system (12 units) due to four software defects that may prevent imaging, corrupt images, or cause unintended shutdowns during clinical use.
Tiffin is recalling 2020-2022 Allegro Red motorhomes because the patio awning may have been improperly installed and could detach while driving, increasing crash and injury risk.
Siemens is recalling 72 units of Artis icono biplane diagnostic imaging systems nationwide due to four software issues that could disable x-ray capability, corrupt diagnostic images, or cause unexpected shutdowns during procedures.
Keystone is recalling 2021-2022 Raptor and 2021 Montana RVs with certain Sailun tires that may experience belt separation. Belt separation could cause loss of vehicle control and increase crash risk.
World Health Products LLC is recalling GAT SPORT JETFUEL DIURETIC capsules because they may contain undeclared milk, a common allergen. The product was distributed across most U.S. states and internationally.
Edge Pharma is recalling approximately 5,335 syringes of Phenylephrine HCl Sterile Solution for Injection nationwide due to lack of assurance of sterility. The product may not meet sterility requirements for safe use.
Edge Pharma is recalling a sterile ophthalmic solution (Phenylephrine HCl/Tropicamide 2.5%/1%) because the manufacturer cannot assure sterility of the product. The recall affects 363 droptainers distributed nationwide.
Tesla is recalling 2020-2022 Model Y, S, X, and 3 vehicles due to a heat pump software error that reduces windshield defrosting performance. This may decrease driver visibility and increase crash risk.
Brownie Points LLC is recalling Brownie Points Schmurtle brownies because the label does not disclose peanuts as an allergen. The product was distributed across the United States in gift baskets.
Games Workshop is recalling about 2,600 KOYO Bounca The Squig Limited Edition Plush toys because the pom-poms can detach, posing a choking hazard to young children. No injuries have been reported.
Edge Pharma, LLC is recalling Methotrexate, USP, Sterile Solution for Injection (125 mg/5mL) due to lack of assurance of sterility. The recall affects 457 syringes distributed nationwide.
About 141,000 Maxtrade Coolster Mountopz youth all-terrain vehicles fail to meet federal safety standards. The ATVs exceed maximum speed limits for their intended age groups and some have parking brakes that do not prevent vehicle movement, posing a risk of serious injury or death.
GE Healthcare is recalling the Vscan Extend ultrasound device because it will not power on when the battery is depleted. This occurs when the device is not turned off before battery removal or is connected to a computer without AC power.