State
73,809 recalls have nationwide distribution and so reach Indiana. 9,598 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,598 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 2,536 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,598 recalls whose distribution notice names Indiana specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Griffith Labs U.S.A. is recalling 50-pound bags of Ranch Seasoning because a whey ingredient used in the product was recalled for potential Salmonella.
Bobcat is recalling approximately 2,700 model year 2015-2018 3400 and 3400XL utility vehicles because the exhaust header pipe can crack, posing burn and fire hazards.
Griffith Labs U.S.A. is recalling 50-pound bags of Cheese & Garlic Seasoning because it may contain Salmonella from a recalled whey ingredient.
Cayenne Medical Inc. is recalling 229 Quattro Link drills because a review of complaints identified a trend for the devices breaking.
Natus Neurology is recalling 462 XLTEK EMU40EX EEG Headboxes because an internal electronic component may degrade, causing the unit to overheat and the plastic case to melt.
Griffith Labs U.S.A. is recalling Pork Flavored Gravy Mix due to the potential presence of Salmonella from a recalled whey ingredient.
Griffith Labs U.S.A. is recalling 50-pound bags of Cheese and Garlic Crouton Seasoning because a whey ingredient used in the product may contain Salmonella.
Griffith Labs U.S.A. is recalling 60 bags of Asiago Peppercorn due to the potential presence of Salmonella from a recalled whey ingredient.
Griffith Labs U.S.A. is recalling 50-pound bags of Butter Garlic Crouton Seasoning because it may contain Salmonella from a recalled whey ingredient.
Siemens Medical Solutions is recalling SOMATOM Scope devices due to a software issue that may cause unnecessary radiation exposure.
Griffith Labs U.S.A. is recalling 67 totes of East Cheddar cheese due to the potential presence of Salmonella from a recalled whey ingredient.
Griffith Labs U.S.A. is recalling 50-pound bags of Italian Crouton Seasoning because it may contain Salmonella from a recalled whey ingredient.
Griffith Labs U.S.A. is recalling Cold Dough Premix because it may contain Salmonella from a recalled whey ingredient.
Griffith Labs U.S.A. is recalling Deep Pan Pizza Dough because it may contain Salmonella from a recalled whey ingredient. The product was distributed nationwide and in Canada.
GE Healthcare is recalling 42 Revolution EVO 3.6 CT systems installed with a specific electrical panel that may not be properly wired to the UPS.
GE Healthcare is recalling 42 Discovery MI CT systems installed with a specific electrical panel that may not be properly wired to the UPS.
Siemens Medical Solutions USA is recalling SOMATOM Perspective 16 CT scanners due to a software issue that may cause unnecessary radiation exposure.
Griffith Labs U.S.A. is recalling 183 bags of Seasoned Crouton Seasoning N5 due to the potential presence of Salmonella from a recalled whey ingredient.
Griffith Labs U.S.A. is recalling 50-pound bags of Romano Garlic Seasoning due to potential Salmonella contamination from a recalled whey ingredient.
West-Ward Columbus Inc is recalling Doxycycline Hyclate 100 mg tablets because they failed to meet dissolution specifications.
Stryker Neurovascular is recalling FlowGate2 Balloon Guide Catheters because the balloon diameter may exceed specifications, potentially causing resistance during use.
GE Healthcare is recalling 42 Discovery RT CT systems nationwide due to a potential wiring defect in the electrical panel that may affect the uninterruptible power supply.
Hetero Labs is recalling 18,288 bottles of Indomethacin 50 mg capsules due to customer complaints of deformed, clumped, or stuck together capsules.
bioMerieux, Inc. is recalling VIDAS LH test kits because internal tests confirmed a decrease in strip signal over time, leading to invalid calibration results.
Major Pharmaceuticals is recalling Doxycycline Hyclate 100 mg tablets because they failed to meet dissolution specifications.