State
72,940 recalls have nationwide distribution and so reach Indiana. 9,555 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,555 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 2,136 (22%) are Severe.
Which agencies issued them
These figures cover only the 9,555 recalls whose distribution notice names Indiana specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 8,600 Viofairy Hair Growth Serum are being recalled because the packaging is not child-resistant as required by the Poison Prevention Packaging Act.
About 21,230 Giraffe and Llama plush toys with clips sold at Hobby Lobby are being recalled because the legs can detach and release small beads.
About 600 Primark The Nightmare Before Christmas Glow-in-the-Dark Coloring Sets are being recalled because the crayons have high levels of strontium and aluminum.
About 1,416 NorthStar hot water pressure washers are being recalled because the fan wheel can fail, causing abnormal burner operation that can produce smoke or bursts of flames.
About 7,000 Sefudun 5% Minoxidil Hair Growth Serum Kit are being recalled because the packaging is not child-resistant as required by the Poison Prevention Packaging Act.
About 21,170 bottles of Bazic Silicone Glue are being recalled because the methanol-containing glue is not in child-resistant packaging and is incorrectly labeled "Non-Toxic".
Autocar is recalling 2023-2026 Xpeditor vehicles because contact with the drive line yoke may damage the Electronic Stability Control unit, increasing crash risk.
About 9,150 LuxJet Submersible LED Lights are being recalled because the lithium coin batteries can be accessed easily by children and the lights lack the warnings required by Reese's Law.
About 320 Urban Arrow FamilyNext Pro Cargo E-Bikes are being recalled because the Fidlock buckle can fail to fully latch when used with children in the cargo area.
About 2,390 Sunneday and Blue Bay above-ground pools 48 inches and taller are being recalled because the compression strap around the pool legs may let a child climb in.
White Castle System is recalling 1,021 cases of White Castle Original Sliders over undeclared milk and soy.
Medline is recalling 35,694 units of the Full Electric Lightweight Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.
Ducati is recalling certain 2025-2026 Streetfighter V4 and Panigale V4 motorcycles because excessive heat may damage the rear brake hose, resulting in a sudden loss of the rear brakes.
Zero Motorcycles is recalling 2024-2025 DS, DSR, DSRP, and DSR/X motorcycles because a twisted front brake hose may leak fluid and reduce braking ability.
Philips is recalling 228 Azurion systems on software version R3.1 over two software issues that may result in loss of imaging, loss of motorized movement, incorrect image content or loss of data.
Merit Medical Systems is recalling its Custom Procedure Kit because the inflation device handle may detach from the syringe during a procedure.
Merit Medical Systems is recalling 328,000 units of the Allwell Angioplasty Pack because the inflation device handle may detach from the syringe during a procedure.
Gold Star Distribution is recalling all human food products distributed from the firm over potential exposure of rodents and rodent activity in the distribution center.
Merit Medical Systems is recalling 173,645 units of the Allwell Inflation Device because the inflation device handle may detach from the syringe during a procedure.
Merit Medical Systems is recalling 18,897 units of its Custom Inflation Kit because the inflation device handle may detach from the syringe during a procedure.
Specialty Process Labs is recalling one lot of Thyroid, USP bulk drug substance because it is subpotent.
ICU Medical is recalling 14,684,607 Tego Connectors because the silicone seal may bulge, separate from the body or tear, which can cause fluid leaks, occluded flow or air infused into the body.
Graviti Pharmaceuticals is recalling 4,212 bottles of Furosemide Tablets, USP 40 mg over the presence of a foreign substance.
Merit Medical Systems is recalling 4,163,123 units of the Merit Medical Inflation Device basixCOMPAK because the inflation device handle may detach from the syringe during a procedure.
Baxter Healthcare is recalling 585 SIGMA Spectrum Infusion Pumps because defective grease on the cam and motor gears could lead to over-infusion or a free-flow situation.