State
72,907 recalls have nationwide distribution and so reach Oregon. 7,525 additional recalls listed Oregon specifically in their distribution scope.
Of the 7,525 recalls naming Oregon we have scored against our rubric, 876 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,803 (24%) are Severe.
Which agencies issued them
These figures cover only the 7,525 recalls whose distribution notice names Oregon 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 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 3,585 model year 2026 Kawasaki Teryx4 H2 and Teryx5 H2 off-road vehicles are being recalled after 19 reports of drive converter sheave breakage.
About 86,040 Kitchen HQ thermal insulated bowls with detachable hinged lids are being recalled after 30 reports of smoking, sparking, melting or fire when microwaved.
Altec Industries is recalling 2024-2026 AC Series Cranes because missing welds on the 26-foot insulating personnel jib may cause the platform to fall, increasing injury risk.
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 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 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 2,100 The Black Sheep Fam Kids' Unisex Jogger Pajama Sets and Girls' Sleepshirts are being recalled for violating the mandatory flammability standard.
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 5,770 Hopelight adult portable bed rails, model F311, are being recalled for violating the mandatory safety standard for adult portable bed rails.
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 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 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 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.
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 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.
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 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.
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.
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 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.
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.
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.