State
72,820 recalls have nationwide distribution and so reach Indiana. 9,554 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,554 recalls naming Indiana we have scored against our rubric, 1,903 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,135 (22%) are Severe.
Which agencies issued them
These figures cover only the 9,554 recalls whose distribution notice names Indiana specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Grand Design is recalling 2026-2027 Lineage RVs because a rooftop fan component may overheat and cause a fire. Dealers will replace the part free of charge.
Tenneco Automotive is recalling NAPA steering inner tie rod ends for certain Ford C-Max, Escape, and Focus models because the stud may separate, causing a loss of steering.
Zoox is recalling Automated Driving Systems because software may fail to detect heavy smoke, increasing crash risk in low-visibility areas.
About 1,400 Flaunt MagSafe Battery Chargers (model E33A) are being recalled because the lithium-ion battery can overheat and ignite. The company has received five reports of the power banks catching fire, including two reports of burns and four reports of property damage.
Volvo Trucks is recalling certain 2026 VNL, VNR, VHD, VN, and VAH vehicles because the steering arm may not be tightly fastened to the steering knuckle, risking loss of steering control and crashes.
Moodooy Adult Portable Bed Rails sold on Amazon violate mandatory safety standards and pose risk of entrapment and asphyxiation. The rails lack required warning labels and users can become trapped within the rail or between the rail and mattress.
BBRKIN and MouTec biometric firearm safes can be opened by unauthorized users, creating a serious injury and death risk. Consumers should immediately stop using the biometric feature and use the key only.
Greenworks Tools recalls Kobalt yard power tools with USB-C batteries due to risk of fire when batteries are charged via the USB-C port while inserted in the tool. The firm received 34 reports of batteries smoking, sparking, or catching fire, with no injuries reported.
Conair is recalling the Cuisinart Propel+ Four Burner 3-in-1 Gas Grill because the tempered glass window in the pizza oven can shatter during use, posing a laceration risk. About 12,660 units were sold.
Best Buy is recalling about 3,820 Insignia Front Control Gas Ranges because the front-mounted knobs can be accidentally activated by humans or pets, creating a fire hazard risk.
WonderStone Infant Walkers sold on Walmart.com violate mandatory infant-walker standards because they can fit through doorways and fail to stop at steps, posing a risk of serious injury or death from falls. No injuries have been reported.
Insulet Corporation is recalling Omnipod DASH Pods worldwide due to external soft cannula damage during manufacturing that can cause insulin to leak around the pod instead of being delivered. This may lead to high blood glucose levels and, in severe cases, diabetic ketoacidosis or death.
BMW is recalling 29,119 vehicles because a corroded starter relay may overheat and short circuit, increasing the risk of a fire.
CareFusion 213, LLC is recalling PurPrep sterile applicators distributed nationwide because unsterilized units intended for further processing were distributed to customers outside the intended channel.
CareFusion 213, LLC is recalling ChloraPrep One-Step (chlorhexidine gluconate and isopropyl alcohol) applicators distributed nationwide. The products were unsterilized and distributed outside the intended channel intended for further processing and sterilization.
Cipla USA, Inc. is recalling Cinacalcet Hydrochloride 90 mg tablets (Lot #5PB0563, expiring 4/30/2027) distributed nationwide due to the presence of N-nitroso-cinacalcet above acceptable daily intake levels, a manufacturing deviation.
Cipla USA, Inc. is recalling Cinacalcet Hydrochloride Tablets, 60 mg due to cGMP deviations involving the presence of N-nitroso-cinacalcet above acceptable daily intake levels.
Lupin Pharmaceuticals is recalling Glucagon Emergency Kits (1mg) nationwide due to a manufacturing process deviation found during stability testing. The gliding force functionality test failed to meet specifications during 12-month testing.
Insulet Corporation is recalling Omnipod (Eros) Pod units due to external soft cannula damage during manufacturing that can cause insulin leakage instead of delivery to the user. High blood glucose levels and serious complications including diabetic ketoacidosis (DKA) or death may result from under-delivery of insulin.
Boston Scientific Corporation is recalling the CRE Wireguided 6-8mm 240cm device worldwide due to a potential sterile breach of the packaging pouches.
Medline is recalling convenience kits containing Swan-Ganz catheters due to failures of the proximal injectate lumen hub that can cause leaks, lumen damage, and breakage, potentially resulting in infection, medication loss, or blood loss.
CareFusion is recalling ChloraPrep One-Step antiseptic applicators because unsterilized units intended for further processing were distributed outside the intended channel, creating a sterility assurance gap.
Medline Industries is recalling reprocessed electrophysiology and ultrasound catheters with residual particles that may cause inflammation, infection, or blood clots if contacted with blood or the heart.
CareFusion 213, LLC is recalling ChloraPrep One-Step chlorhexidine gluconate and isopropyl alcohol applicators distributed nationwide because unsterilized units intended for further processing were distributed through the wrong channels.
Windstone Medical Packaging is recalling 1,080 DSAEK Pack-RX surgical convenience kits containing Webcol Large Alcohol Prep Pads contaminated with Paenibacillus phoenicis bacteria discovered during a sterilization audit.