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.
Caito Foods LLC is recalling Delish Vegetable Garden Salad because an ingredient tested positive for Cyclospora. The product was distributed in Michigan, Indiana, and California.
GE Medical Systems is recalling Vivid E90 ultrasound systems because the power cord may break and expose electrical conductors, posing a risk of shock.
GE Medical Systems is recalling 12,426 LOGIQ 9 ultrasound systems because the power cord may break and expose electrical conductors, creating a shock hazard.
Caito Foods LLC is recalling Small Garden Salad because an ingredient tested positive for Cyclospora. The product was distributed in Michigan, Indiana, and California.
Lakota is recalling 2018-2019 Bighorn, Charger, and Colt trailers because a blocked refrigerator roof vent may increase fire risk or allow carbon monoxide entry.
Fresh Express is recalling expired McDonald's Whole Green Leaf Salad after a test detected the Cyclospora organism.
GE Medical Systems is recalling Vivid E80, E90, and E95 ultrasound systems because the power cord may break and expose electrical conductors, creating a shock hazard.
Caito Foods LLC is recalling Garden Highway Vegetable Garden Salad because an ingredient tested positive for Cyclospora.
Caito Foods LLC is recalling Garden Salad with Homestyle Ranch Dressing because an ingredient tested positive for Cyclospora.
Fresh Express is recalling expired McDonald's salad ingredients after a positive test for the Cyclospora organism.
GE Medical Systems is recalling 12,426 LOGIQ E9 ultrasound systems because the power cord side may break, exposing electrical conductors and creating a risk of electric shock.
GE Medical Systems is recalling 12,426 Vivid E9 ultrasound systems because the power cord may break and expose electrical conductors, posing a risk of electric shock.
Quasar Bio-Tech is recalling 6,783 Pure Rayz Light Therapy Systems because the packaging and manuals make claims about collagen and elastin production that were not cleared by the FDA.
Virtus Pharmaceuticals is recalling Virt-Nate and Virt Gard tablets because the labels do not reflect the correct amount of Dietary Folate Equivalents.
Akorn, Inc. is recalling Ethosuximide Capsules, 250 mg, due to out-of-specification results for an unspecified impurity.
Inspire Medical Systems is recalling 93 Inspire II Implantable Pulse Generators because the device registration labels contain an incorrect use-by date.
Quasar Bio-Tech is recalling the Baby Quasar Plus Light Therapy System because it lacks FDA clearance for specific collagen and elastin claims.
Virtus Pharmaceuticals is recalling Virt-Nate and Virt Gard Tablets because the labels do not reflect the correct amount of Dietary Folate Equivalents.
Quasar Bio-Tech, Inc. is recalling the Quasar MD Plus Light Therapy System because the packaging and user manuals contain claims for collagen and elastin production that were not cleared by the FDA.
Zimmer Dental Inc. is recalling 299 units of Tapered Screw-Vent Implants because the inner package labels display incorrect item, lot, and size information.
Ford is recalling 2018 Ford Edge and Lincoln MKX vehicles because shorter-than-intended door striker bolts may cause doors to open in a crash, increasing injury risk.
Mercedes-Benz is recalling 2018 C300, C300 4MATIC, C63 AMG, and C63S AMG vehicles because incorrect rear window bonding may cause the glass to detach, creating a road hazard.
Continental Tire is recalling specific Conti Hybrid HS3 tires because visible cords through the innerliner can cause sudden air loss and loss of vehicle control.
Cost Plus World Market is recalling Hartley flip daybeds because the bottom cushion fails federal flammability standards, posing a fire hazard.
Emerson Tool Company is recalling RIDGID wet/dry vacuums because the on/off switch can dislodge, exposing energized wiring and posing a shock hazard.