State
72,971 recalls have nationwide distribution and so reach Kansas. 5,725 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,725 recalls naming Kansas we have scored against our rubric, 1,046 (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 5,725 recalls whose distribution notice names Kansas specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Orascoptic custom loupes configured with Phantom frames are recalled because loupe nose pads containing nickel may cause an allergic reaction, following complaints. 10,611 units are affected.
Magna International is recalling rearview cameras installed on certain Ford and Chrysler vehicles because they may display a blank or inverted image, increasing crash risk.
Orascoptic custom loupes with Dragonfly frames are recalled because loupe nose pads containing nickel may cause an allergic reaction, following complaints. 15,245 units are affected.
Ford is recalling specific 2015-2019 vehicles because the rearview camera may display a distorted, inverted, or blank image, increasing crash risk.
GE HealthCare OEC 9800 and OEC 9900 Elite C-arm systems are recalled because impacted units are missing the full layer of lead tape in the collimator covers, slightly increasing radiation exposure.
Bardex Lubri-Sil I.C. Foley catheters and related tray systems are recalled because the catheter may have an obstructed lumen, which may prevent the bladder from draining. 175,158 units are affected.
Orascoptic Phantom Essential Kits are recalled because loupe nose pads containing nickel may cause an allergic reaction, following complaints. 74 kits are affected.
GE HealthCare OEC 9800 C-arm systems are recalled because impacted units are missing the full layer of lead tape in the collimator covers, slightly increasing radiation exposure.
Corin Operating Tables are recalled because interference, such as from high-frequency surgical equipment used at the same time, can leave the table unresponsive to both the remote control and the override panel.
Sandoz Enoxaparin Sodium Injection bags labeled 80 mg/0.8 mL were found to contain 30 mg/0.3 mL prefilled syringes. 10 bags distributed in Kansas are affected.
Orascoptic Dragonfly Nose Pad Accessory Kits are recalled because loupe nose pads containing nickel may cause an allergic reaction, following complaints. 743 kits are affected.
ReliOn Sterile Alcohol Swabs distributed by Walmart are recalled nationwide because isopropyl alcohol levels fall below the labeled concentration. The recall covers 3,456,000 pads.
Orascoptic Phantom Nose Pad Accessory Kits are recalled because loupe nose pads containing nickel may cause an allergic reaction, following complaints. 22 kits are affected.
Chocolate Chip Cookie Dough ice cream in half gallon cartons carrying a Moo-llennium Crunch lid is recalled for undeclared almond, walnut and pecan. 16,532 half gallons are affected.
H-E-B inControl Sterile Alcohol Pads, 100 per container, are recalled nationwide because isopropyl alcohol levels fall below the labeled concentration. The recall covers 300,000 pads.
Hostess Ding Dongs in twin packs and 10- and 16-count cartons are recalled for mold, which the firm traced to a malfunctioning cooler after customer complaints rose. 60,630 cases are affected.
ELEOS Bowed Canal Filling Stems are recalled because an unidentified substance of unknown impact was found on devices during a retrospective evaluation. 30 units are affected.
Rite Aid Pharmacy first aid alcohol prep pads are recalled nationwide because isopropyl alcohol levels fall below the labeled concentration. The recall covers 984,000 pads.
ELEOS Segmental Limb Salvage System straight splined slotted stem extensions are recalled because an unidentified substance of unknown impact was found on devices during a retrospective evaluation. 554 units are affected.
Atlantis IO FLO-S Kits are recalled because a thread defect stops the device fully engaging an implant or analog, engaging about two rotations instead of five. 102 units are affected.
STA Satellite analyzers are recalled because of the potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen reagents in unfractionated and low molecular weight heparin applications. 3,650 units are affected.
Two NovoTHOR Gen 3.0 Reg PRX units are recalled because a failed welded nut may shear off, detaching a gas strut from the canopy and making the canopy difficult to lift.
STA-Liquid Anti-Xa 4 kits are recalled because of the potential for contamination by Stago Fibrinogen reagents in unfractionated and low molecular weight heparin applications. 116,600 units are affected.
BD PhaSeal closed system drug transfer devices are recalled because they were shipped to the US market without a US version of the instructions for use. 3,884,670 units are affected.
BD Pyxis MedStation and Anesthesia Station devices are recalled because antivirus software was not consistently installed during implementation. 8,353 devices are affected, 6,738 of them in the US.