State
72,940 recalls have nationwide distribution and so reach Kansas. 5,723 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,723 recalls naming Kansas we have scored against our rubric, 1,045 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,228 (21%) are Severe.
Which agencies issued them
These figures cover only the 5,723 recalls whose distribution notice names Kansas specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
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 2,448 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
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.
Asteria Health is recalling 133 pellets of ESTRADIOL, 22 mg sterile pellets over the potential presence of metal particulate matter.
Asteria Health is recalling 194,336 pellets of Testosterone, 200 mg sterile pellets over the potential presence of metal particulate matter.
Asteria Health is recalling 2,442 pellets of ESTRADIOL, 25 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.
Fresenius Kabi Compounding is recalling 10,548 bags of thiamine HCl 500 mg in sodium chloride injection over a lack of assurance of sterility.
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 120 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
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 1 of the Azurion 7 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
McCain Foods USA is recalling 21,557 cases of Ore-Ida Tater Tots shaped potatoes over foreign material described as small hard plastic fragments.
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 70,959 pellets of Testosterone, 50.0 mg sterile pellets over the potential presence of metal particulate matter.
Asteria Health is recalling 50,990 pellets of ESTRADIOL, 6 mg sterile pellets over the potential presence of metal particulate matter.
Amerisource Health Services is recalling 31,676 packages of Oxycodone Hydrochloride Tablets 5 mg over card seal defects that let tablets fall out of their cavities.
Medline is recalling 8,445 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 670 pellets of Testosterone 75mg, Anastrozole 4mg sterile pellets over the potential presence of metal particulate matter.
Medline is recalling 21,854 units of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Hologic is recalling 681,870 Brevera Breast Biopsy System disposable 9 gauge needles because particulates in affected devices can be deposited into breast tissue during use.
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.
Philips is recalling 52 IQon Spectral CT units because fasteners attaching the rotor to the gantry bearing may not be torqued to specification.
Steris is recalling 10 units of the Barco MNA with HexaVue IP Integration System because the supplier used the incorrect configuration file for a limited batch of adapter components.
Alphatec Spine is recalling 7 ATEC Lateral Navigation Disc Prep Instruments due to a design issue where the navigated array connection geometry is incorrect.