State
72,907 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 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 2,500 Arctic Zone Titan Pro 40-can iceless coolers are being recalled because the latch magnet can detach, posing a choking hazard.
About 595 Houoto 642-2150V pool drain covers are being recalled because they lack required product markings under the Virginia Graeme Baker Pool and Spa Safety Act.
About 5,770 Hopelight adult portable bed rails, model F311, are being recalled for violating the mandatory safety standard for adult portable bed rails.
Great Dane is recalling 2026 Champion dry van trailers because deck pins may break, causing the liftgate platform to fall and increasing injury risk.
About 254,000 Sloosh dive sticks, sold in packages of Sloosh water toys model 40041, are being recalled because they exceed the compress limit under the federal dive sticks ban.
About 1,101 model year 2019-2025 UMAX Bistro and Bistro Deluxe vehicles are being recalled because the weight capacity certification label is inaccurate.
KayserBett IDA pediatric care beds are being recalled because the hand control can be operated by children, creating a risk of entrapment and serious injury or death.
BD Spinal Trays containing both a Whitacre 25 G and a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 290 units affected.
The Ivenix Infusion System Large Volume Pump software is being recalled because a software anomaly can report a false battery-health value and trigger a shutdown alarm.
Alfredo Sauce in 3 lb 7 oz sealed poly bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.
BD Spinal Trays with a Whitacre 24 G needle, catalog numbers 400868 and 405652, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,550 units affected.
BD Spinal Trays with Quincke needle 25 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,130 units are affected.
BD Spinal Trays with Whitacre needle 25 G, catalog numbers 405637 and 405707, are being recalled as a sub-recall of the Huons bupivacaine product recall. 5,940 units are affected.
BD Spinal Trays with a Whitacre 25 G needle, catalog number 405658, are being recalled as a sub-recall of the Huons bupivacaine product recall. 150 units affected.
BD Spinal Trays with Whitacre needle 25 G, spanning nine catalog numbers, are being recalled as a sub-recall of the Huons bupivacaine product recall. 13,320 units affected.
Birch Benders Sweet Potato Pancake and Waffle Mix, 12 oz, is being recalled because of undeclared egg. The recall covers 5,340 cases.
BD Spinal Trays with Whitacre needle 22 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 330 units are affected.
BD Spinal Trays with Whitacre needle, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall.
Cheese Sauce Mix and Creamier Cheese Sauce Mix are being recalled because they contain a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.
Spinocan spinal needle procedure kits are being recalled because they contain Bupivacaine Hydrochloride in Dextrose Injection subject to the Huons recall. 16,080 units affected.
Aramark Cheese Sauce New & Improved in 25 lb bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.
Spinal needle procedure kits containing Bupivacaine Hydrochloride in Dextrose Injection are being recalled after the drug's manufacturer issued a voluntary recall. 582,030 units are affected.
Design Options spinal needle anesthesia procedure kits are being recalled because they contain Bupivacaine Hydrochloride in Dextrose Injection subject to the Huons recall.
BD Spinal Trays with a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 990 units are affected.
Cold Prep Cream Sauce in 20 lb bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.