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.
AvKARE is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
New Flyer is recalling 386 XDE40, XDE60, and XDE35 transit buses because pressure switches may fail, causing a loss of drive and increasing crash risk.
AvKARE is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
GE Medical Systems is recalling Vivid E7 ultrasound systems because the power cord may break and expose electrical conductors, creating a risk of electric shock.
AvKARE is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
AvKARE is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
BMW is recalling 2018-2019 X6 and X6 M vehicles because wheel bolts may not have been properly tightened, which could loosen and break, increasing crash risk.
AvKARE is recalling specific lots of Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Highland Ridge RV is recalling 2019 Open Range and Mesa Ridge travel trailers because missing inner bearing races may cause hub failure and increase crash risk.
McKesson is recalling 1,531 cartons of Megestrol Acetate Oral Suspension because the drug is supra-potent. The recall is voluntary and nationwide.
Fresh Express is recalling 482 cases of Chopped Romaine 1 lb after a test detected the Cyclospora organism. The product was distributed in 15 U.S. states.
Jayco is recalling 2019 White Hawk, Jay Flight, and Jay Flight SLX travel trailers because missing inner bearing races may cause hub overheating and axle separation.
Caito Foods LLC is recalling Small Caesar Salad because an ingredient tested positive for Cyclospora. The product was distributed in Michigan, Indiana, and California.
McKesson Israel Ltd. is recalling McKesson Cardiology Hemo software version 13.0 because the Real Time Monitor may fail to display physiological signals under certain circumstances.
Caito Foods LLC is recalling 8 oz Vegetable Garden Salad because an ingredient tested positive for Cyclospora. The product was distributed in Michigan, Indiana, and California.
Caito Foods LLC is recalling Delish Greek Salad because an ingredient tested positive for Cyclospora. The product was distributed in Michigan, Indiana, and California.
Caito Foods LLC is recalling 11 oz. Greek Salad with Greek Feta Dressing because an ingredient tested positive for Cyclospora. The product was distributed in Michigan, Indiana, and California.
Steris Corporation is recalling 2,889 V-PRO low temperature sterilization systems because they may fail to detect expired sterilant cups after a power cycle.
Caito Foods LLC is recalling Large Garden Salad because an ingredient tested positive for Cyclospora. The product was distributed in Michigan, Indiana, and California.
Caito Foods LLC is recalling Garden Highway Mt. Olympus Greek Salad because an ingredient tested positive for Cyclospora.
Caito Foods LLC is recalling Large Caesar Salad because an ingredient tested positive for Cyclospora. The product was distributed in Michigan, Indiana, and California.
Caito Foods LLC is recalling deLish Garden side salad because an ingredient tested positive for Cyclospora. The product was distributed in Michigan, Indiana, and California.
Hitachi is recalling VidiStar PACS software versions 3.10.5 and 3.10.6 because a defect may cause images from multiple patients to appear in a single study.
GE Medical Systems is recalling 12,426 Vivid 7 ultrasound systems because the power cord may break and expose electrical conductors, creating a shock hazard.
GE Medical Systems is recalling 12,426 Vivid E95 ultrasound systems because the power cord may break and expose electrical conductors, creating a shock hazard.