State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
CSM Bakery Products is recalling 45 lb. boxes of Safeway Chocolate Buttercreme Base because pieces of plastic polymer were introduced into the sugar system.
Safavieh is recalling Aura and Silas 3-drawer chests because they can tip over or entrap children if not anchored to the wall.
COVIDIEN LLC is recalling 2,180 units of Endo GIA Ultra Universal Staplers because the sterile barrier may be compromised, increasing the risk of infection.
Nobel Biocare is recalling Dense Bone Drills because a packaging sealing issue may compromise sterility during shelf life.
CSM Bakery Products is recalling 43 lb. pails of Glossy White Icing distributed by Krispy Kreme because pieces of plastic polymer were introduced into the sugar system.
Cardinal Health is recalling Presource Procedure Packs containing AAMI Level 3 surgical gowns because they may not be sterile due to improper environmental conditions during manufacturing.
Nobel Biocare is recalling Dense Bone Drills because a packaging defect may compromise sterility during shelf life.
Custom Fire is recalling one 2017 Side Mount Pumper because the foam pump system can overheat and fail, making firefighting foam unavailable.
Siemens is recalling 475 Luminos Agile Max X-ray systems because a bypass key can override collision controls, creating a risk of collision with obstacles or persons.
Nobel Biocare is recalling 423 implant retrieval instruments because a packaging defect may compromise sterility during shelf life.
Philips is recalling 131 CombiDiagnost PCF X-ray systems due to a software error that locks the table and an incorrectly installed thermos switch.
The FDA is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that may compromise sterility.
Siemens Medical Solutions USA, Inc. is recalling 46 Luminos dRF Max digital radiography systems due to a software bug that may assign one image to two different patients, potentially affecting medical diagnosis.
Nobel Biocare is recalling 264 tapered dental drills because a packaging sealing defect may compromise sterility during shelf life.
CSM Bakery Products is recalling 18 lb. pails of Simplicious Cream Cheese Icing because pieces of plastic polymer were introduced into the sugar system.
Daimler Trucks North America is recalling 2017-2020 Thomas Built Buses Saf-T-Liner C2 school buses because the exterior warning lights and stop sign may fail, increasing injury risk.
CSM Bakery Products is recalling 43 lb. pails of White 'n Glossy Icing donut icing because pieces of plastic polymer were introduced into the sugar system.
Siemens Healthcare Diagnostics is recalling Dimension Vista Enzymatic Creatinine reagent because it may produce falsely depressed results for patients taking phenindione.
Nobel Biocare is recalling 197 implant retrieval instruments because a packaging defect may compromise sterility during shelf life.
Home Depot is recalling approximately 200 4-Drawer Whitewash Chests because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards.
Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Suture due to potential packaging integrity issues that may impact the humidity or sterility barrier.
Green Water, LLC is recalling Taspen's Organics Respiratory Tea because it contains Coltsfoot, an ingredient not intended for internal use.
Cardinal Health is recalling Presource Procedure Packs containing AAMI Level 3 surgical gowns because they may not be sterile. This could increase the risk of surgical site infections.
Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Suture 13-0 due to potential packaging integrity issues that may impact sterility.
Siemens is recalling 475 Luminos Agile Max devices due to a software bug that may assign one image to two patients, potentially affecting diagnosis.