State
73,576 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, 1,913 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,529 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,592 recalls whose distribution notice names Indiana specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Velvet Ice Cream Company is recalling Super Dip Neapolitan ice cream pails due to potential Listeria monocytogenes contamination.
Velvet Ice Cream Company is recalling Discount Drug Mart Vanilla Ice Cream because it may be contaminated with Listeria monocytogenes.
Creative Foods Inc. is recalling Bueno Coffee Substitute Pecan Praline because it contains undeclared peanut and barley, posing a risk to individuals with allergies or celiac disease.
Velvet Ice Cream Company is recalling Velvet Caramel Pecan ice cream cartons potentially contaminated with Listeria monocytogenes.
Equipment Technology, L.L.C. is recalling 87 aerial work platform vehicles due to inadequate welds that could cause the aerial unit to fail during use.
Velvet Ice Cream Company is recalling Super Dip Superfriends Ice Cream due to potential Listeria monocytogenes contamination. The product was distributed in nine states.
Velvet Ice Cream Company is recalling Olde Tyme Vanilla ice cream due to potential Listeria monocytogenes contamination. The product was distributed across nine states.
Velvet Ice Cream Company is recalling Buckeye Sandwich ice cream bars due to potential Listeria monocytogenes contamination. The product was distributed across nine states.
A-S Medication Solutions is recalling Health Essentials Kits containing Acetaminophen 500mg tablets. The bottles were incorrectly labeled with prescription drug labels instead of OTC labels.
Velvet Ice Cream Company is recalling Buehler's Vanilla Ice Cream because it may be contaminated with Listeria monocytogenes, a bacterium that can cause serious illness.
QMart is recalling Burro en Primavera capsules because FDA analysis found unapproved tadalafil and/or sildenafil.
Velvet Ice Cream Company is recalling specific lots of Velvet Vanilla Bean ice cream due to potential Listeria monocytogenes contamination.
Velvet Ice Cream Company is recalling Discount Drug Mart Chocolate Swirl Ice Cream due to potential Listeria monocytogenes contamination.
Velvet Ice Cream Company is recalling Velvet Birthday Cake 3 Gallon Tubs due to potential Listeria monocytogenes contamination. The product was distributed across nine states.
Velvet Ice Cream Company is recalling Velvet Blackberry Cobbler due to potential Listeria monocytogenes contamination. The product was distributed across nine states.
BMW is recalling 2021 230i and M240i vehicles because roof liner supports may detach and fall into the cabin, increasing injury risk during a crash.
ETI is recalling 2019-2020 ETC 37 IH vehicles because tilt cylinders may fail, causing unintentional bucket movement that increases injury risk.
Velvet Ice Cream Company is recalling Whale of Pail Vanilla Gallon Plastic Tubs potentially contaminated with Listeria monocytogenes.
Velvet Ice Cream Company is recalling Buckeye Classic ice cream due to potential Listeria monocytogenes contamination.
Velvet Ice Cream Company is recalling Super Dip Chocolate Pail Ice Cream due to potential Listeria monocytogenes contamination.
Velvet Ice Cream Company is recalling Kentucky Praline Pecan ice cream due to potential Listeria monocytogenes contamination.
Velvet Ice Cream Company is recalling Triple Chocolate Chunk ice cream potentially contaminated with Listeria monocytogenes.
Velvet Ice Cream Company is recalling Super Dip Cookies n Cream Ice Cream due to potential Listeria monocytogenes contamination.
Velvet Ice Cream Company is recalling Velvet Vanilla Lovers Trio 56oz cartons potentially contaminated with Listeria monocytogenes.
QMart is recalling Imperial Platinum 2000 capsules because FDA analysis found unapproved ingredients tadalafil and/or sildenafil.