State
72,936 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 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Medline is recalling 141,971 of its 14 Fr Suction Catheter Kits because an 8 Fr catheter may have been packed in place of the required 14 Fr catheter.
Asteria Health is recalling 24,099 pellets of ESTRADIOL, 10 mg sterile pellets over the potential presence of metal particulate matter.
Asteria Health is recalling 62,581 pellets of Testosterone, 87.5 mg sterile pellets over the potential presence of metal particulate matter.
Philips is recalling 5 of the Azurion 7 M20 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Toyota is recalling certain 2025-2026 Lexus LX600 vehicles due to a potential transmission solenoid failure that can damage the transmission, causing loss of drive power or fluid leaks that increase crash and fire risk.
Philips is recalling 3 units of the Spectral CT 7500 on Rails because fasteners attaching the rotor to the gantry bearing may not be torqued to specification.
Fresenius Kabi Compounding is recalling vancomycin HCl 2 grams in 500 mL sodium chloride injection over a lack of assurance of sterility.
Asteria Health is recalling 4,599 pellets of Testosterone 100mg, Triamcinolone Acetonide 20mcg sterile pellets over the potential presence of metal particulate matter.
Asteria Health is recalling 133 pellets of ESTRADIOL, 22 mg sterile pellets over the potential presence of metal particulate matter.
Asteria Health is recalling 1,758 pellets of Testosterone, 62.5 mg sterile pellets over the potential presence of metal particulate matter.
Philips is recalling 283 Spectral CT units because fasteners attaching the rotor to the gantry bearing may not be torqued to specification.
Medline is recalling 4,300 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Fresenius Kabi Compounding is recalling 1,410 bags of Ketamine HCl injection over a lack of assurance of sterility.
Philips is recalling 1 of the Azurion 7 B20 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Philips is recalling 291 units of the Azurion 3 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Asteria Health is recalling 100 pellets of Testosterone 100mg, Anastrozole 4mg (4.5) sterile pellets over the potential presence of metal particulate matter.
Medline is recalling 450 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Philips is recalling 47 units of the Brilliance iCT because fasteners attaching the rotor to the gantry bearing may not be torqued to specification.
Asteria Health is recalling 7,840 pellets of Testosterone 200mg, Triamcinolone Acetonide 40mcg sterile pellets over the potential presence of metal particulate matter.
Fresenius Kabi Compounding is recalling 10,548 bags of thiamine HCl 500 mg in sodium chloride injection over a lack of assurance of sterility.
Medline is recalling 1,350 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Asteria Health is recalling 14,848 pellets of ESTRADIOL, 15 mg sterile pellets over the potential presence of metal particulate matter.
Asteria Health is recalling 715 pellets of ESTRADIOL, 37.5 mg sterile pellets over the potential presence of metal particulate matter.
Intuitive Surgical is recalling 47 da Vinci 5 Surgeon Console Viewer Displays manufactured with outdated firmware, which may cause loss of the 3D surgical field or complete visualization loss.
Philips is recalling 655 units of the Azurion 7 B12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.