State
73,576 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 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
REV Ambulance Group Orlando is recalling 2019-2021 Type I and IX ambulances because LCD displays may lock up, potentially delaying emergency efforts.
Rosenbauer America is recalling specific fire trucks because rear lights may be too bright, potentially blinding other drivers and increasing crash risk.
Gillig is recalling 229 CNG-powered buses because insufficient roof door overlap may allow accidental opening, increasing crash risk.
Blue Bird is recalling 2020-2022 Vision and All American school buses because a check valve may fail to isolate air, potentially causing unintended spring brake application and increasing crash risk.
Blue Bird is recalling 96 2022 Vision and All American transit buses because a check valve defect may cause unintended spring brake application, increasing crash risk.
Kawasaki is recalling about 70 2021 BRUTE FORCE 750 ATVs because loose fuel pump bolts can cause fuel leaks and fire. No injuries have been reported.
Kawasaki is recalling about 100 2021 Teryx off-highway utility vehicles because loose fuel pump bolts can cause fuel leaks and fire. No injuries have been reported.
HME is recalling 2013-2021 AF1, 1871, and SFO vehicles because cracked wiring insulation may cause aerial controls to fail, creating a shock risk.
Navistar is recalling certain 2019-2021 International LT and RH trucks due to wrist pin cracks that can cause connecting rod failure and engine stalls. Affected owners should contact their dealer for free repair.
Chrysler is recalling 2020-2021 Dodge Durango vehicles because the side curtain air bag fastener may be loose or missing. A loose fastener could cause incorrect air bag deployment, increasing injury risk.
Dennis Eagle is recalling 2017-2021 Elite and Proview vehicles because documents may list the wrong weight rating, potentially leading to overloading and crashes.
YYBA is recalling Welmate Lidocaine Numbing Cream because the packaging is not child-resistant, posing a risk of poisoning to young children.
Nissan is recalling 2021 Rogue vehicles because the rear brake calipers may be missing an internal bushing, causing brake fluid to leak and reducing braking performance, increasing the risk of a crash.
HME is recalling 2016-2021 AF1 and 1871 vehicles because the self-leveling function may malfunction, causing the aerial bucket to move unexpectedly and increasing injury risk.
Dennis Eagle is recalling 2017-2021 Elite and Proview vehicles because the hard copy owner's manual was not supplied, which may lead to improper operation.
Spartan Chemical is recalling 19,044 containers of Lite'n Foamy Lemon Blossom Hand Sanitizer because a lot tested positive for Burkholderia multivorans.
Novo Nordisk is recalling Levemir FlexTouch insulin pens stored below 32°F, which may cause lack of efficacy and damage to the cartridge and pen-injectors.
Novo Nordisk is recalling Fiasp insulin cartridges stored below 32°F, which may cause lack of efficacy and damage to the cartridge and pen-injectors.
Spartan Chemical Co Inc is recalling 400 gallons of Antiseptic Hand Cleaner due to CGMP deviations. The product was distributed nationwide in the US, Puerto Rico, and Mexico.
Novo Nordisk is recalling Fiasp insulin pen samples stored below 32°F. The temperature abuse may cause lack of efficacy and damage to the cartridge and pen-injectors.
Bentley is recalling 2021 Bentayga vehicles because a rear axle lock nut may break due to stress corrosion, potentially causing loss of control.
Novo Nordisk is recalling Xultophy 100/3.6 samples stored below 32°F. The temperature abuse may cause lack of efficacy and damage to the cartridge and pen-injectors.
Novo Nordisk is recalling TRESIBA (insulin degludec) samples stored below 32°F, which may cause lack of efficacy and damage to the cartridge and pen-injectors.
Novo Nordisk is recalling Fiasp (insulin aspart injection) samples stored below 32°F, which may cause lack of efficacy and damage to the cartridge and pen-injectors.
Novo Nordisk is recalling specific lots of TRESIBA insulin pens because they were stored below 32°F, which may reduce efficacy and damage the device.