State
73,598 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, 1,908 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,534 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,592 recalls whose distribution notice names Indiana specifically. The 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
W.L. Gore is recalling GORE TAG stent grafts because the delivery catheter could not be withdrawn after implantation.
GE Healthcare is recalling 64 CT scanners worldwide because incorrect settings may cause smudge artifacts that could be mistaken for pathology.
Intuitive Surgical is recalling one da Vinci Xi Endoscope Controller because improper calibration may cause the endoscope tip to reach higher temperatures, potentially leading to thermal tissue injury.
Thor Motor Coach is recalling 2010-2011 Four Winds Montecito motorhomes because a transfer switch may fail due to heat, increasing fire risk.
Philips is recalling 8,942 sterilizable defibrillator paddles because standard checks may miss a specific failure mode. An updated test procedure is available to detect the issue.
Transcraft is recalling 2016-2021 Platform trailers because adjustable wheel stops may detach, increasing the risk of crash or injury.
YETI is recalling Rambler 20 oz Travel Mugs with Stronghold Lids because the magnetic slider can eject, causing hot liquid to spill and posing burn risks.
Hu Products is recalling chocolate-covered cashews that may contain undeclared almonds. Consumers with tree nut allergies should not consume the product.
Nurture Inc. is recalling Happy Tot Superfoods Gluten Free Oat Bars due to mold growth. The product is intended for toddler consumption.
Boehringer Ingelheim is recalling specific lots of Catapres tablets because an extraneous peak was observed during dissolution testing.
Boehringer Ingelheim is recalling specific Catapres tablets because an extraneous peak was observed during dissolution testing. The recall covers products distributed nationwide and in Puerto Rico.
Exactech is recalling 25 Equinoxe Platform Fracture Stems because they may be incorrectly laser marked as right stems instead of left stems.
Siemens Medical Solutions is recalling 22 Artis one systems because the examination room monitor may become intermittently dysfunctional, causing display issues.
Boehringer Ingelheim is recalling Catapres tablets because an extraneous peak was observed during dissolution testing. The affected lots were distributed nationwide and in Puerto Rico.
Boston Scientific is recalling one unit of the Visual-ICE MRI Cryoablation System Mobile Connection Panel due to an incorrectly installed base.
Exactech is recalling 12 Equinoxe Platform Fracture Stems because they may be incorrectly laser marked as right stems when they are left stems.
RTI Surgical is recalling 420 units of Streamline TL Navigation System taps because they have experienced binding with other devices.
Nurture Inc. is recalling Happy Kid Gluten Free Fruit & Oat Bars due to mold growth. Consumers should stop eating the product and return it to the store.
Nurture Inc. is recalling Happy Tot Superfoods Gluten Free Oat Bars because mold growth was observed. The affected bars are intended for toddler consumption.
Jarrow Formulas is recalling 533 units of N-A-C 500 mg capsules because they were mislabeled as a different product.
Triple E RV is recalling 143 Wonder motorhomes because a control center component can overheat and cause a fire.
Kawasaki is recalling 2018-2020 Ninja H2 SX motorcycles because a software defect may cause gear fracture and engine lockup, increasing crash risk.
Mercedes-Benz is recalling 2019 GLA 250 vehicles because a loose engine compartment fusebox may damage fuses and disrupt critical safety systems, increasing crash risk.
Mercedes-Benz is recalling certain 2020-2021 GLE models because the middle seat belt buckle may fall into a gap, rendering it inoperable and leaving occupants unrestrained.
Certain 2020-2021 Keystone Cougar trailers with solar packages have incorrectly wired inverters that may energize shore power connections, creating a risk of electrical shock.