State
72,907 recalls have nationwide distribution and so reach Nebraska. 4,547 additional recalls listed Nebraska specifically in their distribution scope.
Of the 4,547 recalls naming Nebraska we have scored against our rubric, 705 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,119 (25%) are Severe.
Which agencies issued them
These figures cover only the 4,547 recalls whose distribution notice names Nebraska specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
International is recalling 2026-2027 HV vehicles because the service brake may take longer than expected to release, increasing crash risk.
About 8,650 model year 2021-2022 Yamaha Drive2 Electric Fleet Golf Cars are being recalled because a misrouted passenger-side brake cable can break during use.
About 17,600 Kidisle single-serve coffeemakers are being recalled after at least 107 reports of unexpected hot liquid or steam release and at least 27 injuries.
About 18,000 Merkury Innovations Hot + Cool Heating and Cooling Fans are being recalled after two reports of the fan catching fire, one causing smoke damage to property.
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 10,354 Timechee Changing Table Dressers are being recalled because they are unstable when not anchored to the wall and violate the mandatory STURDY Act standard.
About 2,100 The Black Sheep Fam Kids' Unisex Jogger Pajama Sets and Girls' Sleepshirts are being recalled for violating the mandatory flammability standard.
About 5,770 Hopelight adult portable bed rails, model F311, are being recalled for violating the mandatory safety standard for adult portable bed rails.
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.
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 3,000 Hasuit 7-Drawer Dressers are being recalled because they are unstable when not anchored to the wall and violate the mandatory STURDY Act standard.
About 6,187 Nimood adult portable bed rails in models C3 Pro, C4 Pro, C5 Pro and C5 Pro 2.0 are being recalled for violating the mandatory safety standard.
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 15,616 plastic tip restraint kits supplied with Childcraft furniture sold by School Specialty are being recalled because the straps can break or degrade.
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.
Design Options spinal needle anesthesia procedure kits are being recalled because they contain Bupivacaine Hydrochloride in Dextrose Injection subject to the Huons recall.
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 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.
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.
Ivenix Infusion System Large Volume Pumps are being recalled because dropping or jarring can loosen the touchscreen input cable, causing random touches or an unresponsive screen.
BD Spinal Trays with Whitacre needle, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall.
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.
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.
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.