State
72,820 recalls have nationwide distribution and so reach Indiana. 9,554 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,554 recalls naming Indiana we have scored against our rubric, 1,903 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,135 (22%) are Severe.
Which agencies issued them
These figures cover only the 9,554 recalls whose distribution notice names Indiana specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Altec is recalling 2021-2023 Service Body vehicles because water leaks into strobe lights, causing electrical short-circuits that increase fire risk.
CPSC is recalling Chillife 5-in-1 Montessori Baby Toy Sets because the pull string teething toy violates safety standards and poses a choking risk to children.
Walmart is reannouncing a recall of Mainstays 9-Drawer Fabric Dressers because they pose tip-over and entrapment hazards that can cause serious injury or death to children.
Diamond Wipes International is recalling MD Wipe Outz Numbing Tattoo Wipes because the packaging is not child-resistant, posing a risk of serious injury or death from child poisoning.
HABA USA is recalling Rainbow Rattle Grasping and Teething Toys because a glued knot can untie, exposing small parts that pose choking and ingestion risks to young children.
Little Loves & Co. is recalling youth clothing sets with drawstrings due to an entrapment hazard that could cause serious injury or death to children.
Excel Industries is recalling about 1,800 accessory LED light kits for Hustler and BigDog ride-on mowers because the light bars can overheat or produce flames.
Whole Foods Market is recalling Heirloom Tomato Salsa because it was made with jalapenos that may be contaminated with Salmonella.
Fresenius Kabi is recalling 625,500 Morphine Sulfate syringes because some were mislabeled and contained Dilaudid instead.
American Regent, Inc. is recalling Papaverine Hydrochloride Injection due to the presence of glass and/or paraformaldehyde particulate matter.
Whole Foods Market is recalling Roasted Corn Guacamole Dip because it was made with jalapenos that may be contaminated with Salmonella.
Whole Foods Market is recalling Mild Guacamole Dip No Tomatoes because it may contain jalapenos contaminated with Salmonella.
Whole Foods Market is recalling Mild Guacamole Dip because it was made with jalapenos that may be contaminated with Salmonella.
Whole Foods Market is recalling Medium Pico de Gallo Guacamole Dip because it may contain jalapenos contaminated with Salmonella.
Whole Foods Market is recalling Mango Pineapple Salsa used in Caribbean Turkey Burgers because the jalapenos may be contaminated with Salmonella.
Whole Foods Market is recalling Spicy Guacamole Dip No Tomatoes because the jalapeños used may be contaminated with Salmonella. The product was sold in 13 states.
Get Fresh Produce is recalling jalapeno peppers due to potential Salmonella contamination. The product was distributed in Illinois, Indiana, Michigan, and Wisconsin.
Whole Foods Trio Dip is being recalled because the jalapeños used in the product may be contaminated with Salmonella.
Whole Foods Market is recalling Spicy Guacamole Dip because the jalapenos used may be contaminated with Salmonella.
Coast Citrus Distributors is recalling bulk jalapeno peppers due to potential Salmonella Javiana contamination. The product was distributed to wholesale distributors and has not been sold at retail.
Whole Foods Market is recalling Pomegranate Guacamole Dip because it may contain jalapenos contaminated with Salmonella. The product was sold in 13 states.
American Regent, Inc. is recalling Aminocaproic Acid Injection due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
American Regent is recalling Multrys (Trace Elements Injection 4) vials due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
American Regent, Inc. is recalling specific lots of Cyanocobalamin injections due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
American Regent, Inc. is recalling Atropine Sulfate injection vials because they contain particulate matter, including hair, glass, and paraformaldehyde.