State
73,741 recalls have nationwide distribution and so reach Kansas. 5,821 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,821 recalls naming Kansas we have scored against our rubric, 1,053 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,485 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,821 recalls whose distribution notice names Kansas specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Synthetopes Inc is recalling Sn-Mertiatide Kits nationwide due to a lack of processing controls. The recall covers all lots remaining within their expiry date.
Geritrex, LLC is recalling Senna Syrup bottles due to reports of atypical odor and unpleasant taste.
Glenmark Pharmaceuticals is recalling Estradiol Vaginal Inserts because the plunger delivery system is not functioning properly.
Cardiocommand Inc. is recalling five units of its Transesophageal Cardiac Pacing and Recording System, Model 7A, due to possible corrosion of the battery contacts.
Conformis is recalling 183 iTotal Hip Replacement System stems nationwide due to a 3mm discrepancy between approved and manufactured neck/head lengths.
Synthetopes Inc. is recalling Sulfur Colloid Reaction Vials nationwide due to a lack of processing controls.
Synthetopes Inc is recalling 82 vials of Sn-DTPA Kit 10 mg nationwide due to a lack of processing controls.
B. Braun Medical Inc. is recalling 40,176 bags of Heparin Sodium in Dextrose because testing showed the drug had lower potency than required by USP specifications.
Philips is recalling Patient Information Center iX software because infusion pump data may be recorded at 100 times the actual rate.
Synthetopes Inc. is recalling Sn-DMSA solution vials nationwide due to a lack of processing controls. The product is not for direct injection.
Philips is recalling IntelliBridge Systems configured with comma decimal separators because infusion pump data may be recorded at 100 times the actual values.
Synthetopes Inc. is recalling Sn-Pyrophosphate Kits because of a lack of processing controls. The recall covers all lots remaining within their expiry dates.
Laird Superfood is recalling Performance Mushrooms because the label incorrectly lists 14 mg of Iron instead of the actual 14 mcg.
Fresenius Kabi USA, LLC is recalling 11,981 vials of Ondansetron Injection, USP, 40 mg / 20 mL, because the product failed impurities and degradation specifications.
Bausch & Lomb is recalling Lotemax ophthalmic gel because it failed stability specifications for viscosity. The recall covers 17,083 bottles distributed nationwide.
Home Meridian is recalling Copeland Corner Curio cabinets sold at Havertys due to tip-over and entrapment hazards that can cause injury.
Isuzu is recalling 2018-2020 FTR and Chevrolet 6500XD vehicles because a steering stopper bolt jam nut may loosen, increasing the turning radius and crash risk.
Farber Specialty Vehicles is recalling 2017 Ford F-550s with Whelen brake lights that may illuminate without the brake pedal being pressed, potentially confusing other drivers.
SVO Group is recalling 2017-2018 Ford E-350 and E-450 shuttle buses because backup camera images may reverse, increasing crash risk.
Farber Specialty Vehicles is recalling 2018 International 4300 SBA vehicles equipped with Whelen brake lights that may illuminate without the brake pedal being pressed.
Altec is recalling 2017-2018 aerial devices because fasteners securing the rotation bearing may break, potentially causing the pedestal to separate from the turntable.
Altec is recalling 328 vehicles due to non-DOT brake line fittings that may leak, causing the parking brake to drag and increasing crash risk.
Forest River is recalling 2017-2018 Berkshire motorhomes because water in the block heater cable can cause corrosion, leading to overheated wiring and fire risk.
Caterpillar is recalling 2015-2019 Progress Rail Sky Trim Hi-Rail vehicles because a support plate may block driver visibility and the boom may detach from the cradle while in motion.
Maserati is recalling 2015-2018 Granturismo vehicles because a defective air bag component may cause the air bag to deactivate or deploy unexpectedly.