State
72,907 recalls have nationwide distribution and so reach North Dakota. 2,921 additional recalls listed North Dakota specifically in their distribution scope.
Of the 2,921 recalls naming North Dakota we have scored against our rubric, 265 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 727 (25%) are Severe.
Which agencies issued them
These figures cover only the 2,921 recalls whose distribution notice names North Dakota 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 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 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 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.
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 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.
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.
Atlan A350 anesthesia workstations are being recalled because units either indicated a piston ventilator failure before use or suffered a mechanical ventilation failure during use.
Atlan A350XL anesthesia workstations are being recalled because units either indicated a piston ventilator failure before use or suffered a mechanical ventilation failure during use.
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 a Whitacre 25 G needle, catalog number 405658, are being recalled as a sub-recall of the Huons bupivacaine product recall. 150 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.
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 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, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall.
BD Spinal Trays with Quincke needle 26 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 890 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.
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.
Design Options spinal needle anesthesia procedure kits are being recalled because they contain Bupivacaine Hydrochloride in Dextrose Injection subject to the Huons recall.
Albertsons store-made chicken caesar salad is being recalled because the contains statement does not declare anchovy. 328 units are affected.
Albertsons store-made Boston Creme Dubai 5-inch cake is being recalled because the contains statement does not declare pistachio. 25 units are affected.
GoodSense Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.