State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
REV is recalling 2018 Fleetwood Jamboree and Holiday Rambler Vesta motorhomes because improperly stripped generator wires may cause an electrical short and fire.
Shippert Medical Technologies is recalling Tissu-Trans SFILL 360 devices because the seal integrity of the sterile packages cannot be assured.
Alcon is recalling 429 ORA Systems with VerifEye+ Carts due to a software error that may cause incorrect intraocular lens power measurements during cataract surgery.
Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 250 because the seal integrity of the sterile packages cannot be assured.
Medtronic is recalling 149 Curved Suction 70 ENT instruments because they fail required pre-use verification checks.
Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 1000 because the seal integrity of the sterile packages cannot be assured.
Penobscot McCrum LLC is recalling Extra Large Seasoned/Battered Jo-Jo Wedges because the product may contain undeclared milk.
Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 2000 because the sterile package seal integrity cannot be assured.
Penobscot McCrum LLC is recalling Valero Baby Wedges with Crisp Coat UC Coating because the product may contain undeclared milk.
Shippert Medical Technologies is recalling Tissu-Trans MEGA 1500 devices because the seal integrity of the sterile packages cannot be assured.
Medtronic Navigation is recalling six kits of ENT suction devices because they fail required pre-use verification checks.
Penobscot McCrum LLC is recalling Medium Battered Jo-Jo Wedges because the product may contain undeclared milk, posing a risk to individuals with milk allergies.
Koogee-Queen Anne, LLC is recalling The Comfy Cow Georgia Butter Pecan Ice Cream due to E. coli and high Coliform Bacteria counts.
New Flyer is recalling 2015-2017 transit buses because the driver's seat belt buckle may be stuck, preventing the belt from latching.
Medtronic is recalling Deep Brain Stimulation lead kits because the depth stop may not secure properly, potentially causing the lead to be placed beyond the intended target.
Koogee-Queen Anne, LLC is recalling 399 pints of The Comfy Cow Double Fold Vanilla Ice Cream due to E. coli and high Coliform Bacteria counts.
Grandma's Herbs is recalling Cholesterol Support dietary supplements because they contain undeclared soy lecithin, a common allergen.
Handi-Craft is recalling Dr. Brown's Natural Bottle & Dish Soap because it may contain harmful bacteria. No injuries have been reported.
Penobscot McCrum LLC is recalling 951 cases of Medium Coated Jo-Jo Wedges because the product may contain undeclared milk.
Koogee-Queen Anne, LLC is recalling The Comfy Cow Intense Dark Chocolate Ice Cream due to E. coli and high Coliform Bacteria counts.
Medtronic Navigation is recalling 277 reusable ENT suction instruments because they fail pre-use verification checks. The devices are used with the StealthStation AxiEM surgical navigation system.
Penobscot McCrum LLC is recalling 18,799 cases of seasoned baby Jo-Jo wedges because the product may contain undeclared milk.
Alcon is recalling 367 ORA Systems with VerifEye because a software error may cause incorrect intraocular lens power measurements during cataract surgery.
Koogee-Queen Anne, LLC is recalling 53 pints of The Comfy Cow Banana Pudding Y'all Ice Cream due to E. coli and high Coliform Bacteria counts.
Shippert Medical Technologies is recalling Tissu-Trans Filtron 100 units because the seal integrity of the sterile packages cannot be assured.