State
73,218 recalls have nationwide distribution and so reach Colorado. 6,945 additional recalls listed Colorado specifically in their distribution scope.
Of the 6,945 recalls naming Colorado we have scored against our rubric, 1,218 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,510 (22%) are Severe.
Which agencies issued them
These figures cover only the 6,945 recalls whose distribution notice names Colorado specifically. The 73,218 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Yoocaa baby loungers fail to meet CPSC safety requirements for infant sleep products, posing suffocation, fall, and entrapment risks. About 4,140 units sold on Amazon from January 2021 through May 2023 are affected; no injuries have been reported.
Lochinvar LLC recalls about 17,370 residential condensing boilers sold under three brand names due to cracking flue collectors that can allow carbon monoxide emission. Consumers should contact installers for free repair or ensure working carbon monoxide alarms are installed.
Grizzly Industrial and Shop Fox wood lathes are being recalled because the cutting tool can break, creating a risk of projectiles striking users or bystanders, and lacerations to users. About 21,300 units are affected.
UncleWu Life is recalling approximately 360 infant bath seats sold on Amazon.com from December 2020 through June 2021. The seats fail federal safety requirements and can tip over, posing a drowning hazard to infants.
Murf Electric Bikes is recalling about 9,000 electric bicycles sold from July 2017 through April 2022 because they do not meet U.S. safety standards and pose fall and injury hazards. The company has received one report of a fall with minor injury.
Dixon Ticonderoga is recalling Creativity Street Assorted Craft Buttons because they contain lead levels that exceed federal limits. Lead can cause adverse health effects if ingested by young children.
Cardinal Health is recalling 1,097,048 Monoject 35 mL syringes due to demonstrated compatibility and recognition issues with infusion pumps. The affected units were distributed nationwide.
B. Braun's Infusomat Large Volume Pump battery pack may sound a false occlusion alarm, causing the device to stop pumping. This interruption of high-risk medications can lead to hemodynamic instability and serious medical consequences.
Cardinal Health recalls approximately 3.1 million Monoject 1 mL Tuberculin Syringes due to demonstrated compatibility and recognition issues with syringe infusion pumps. Nationwide distribution affected.
ResMed recalls Astral ventilators due to a battery fault that can cause sudden power loss. The backup alarm system may fail to alert users due to supercapacitor degradation.
Cardinal Health is recalling Monoject 6 mL Luer-Lock syringes (approximately 3.9 million units) nationwide due to demonstrated recognition and compatibility issues with syringe infusion pumps.
Cardinal Health is recalling 4.9 million Monoject 20 mL Luer-Lock syringes due to compatibility and recognition issues with infusion pumps. Affected lot numbers from 2022 and 2023 were distributed nationwide.
Toyota is recalling 2013-2018 RAV4 vehicles because certain replacement 12-volt batteries may not fit properly, potentially causing a short circuit and fire.
The Infusomat Large Volume Pump may incorrectly sound an occlusion alarm and stop delivering high-risk medications, potentially causing serious complications.
Cardinal Health recalls 3 million Monoject 12 mL Luer-Lock syringes due to demonstrated compatibility issues with syringe infusion pumps that may affect medication delivery.
Cardinal Health is recalling 457,200 Monoject 60 mL Luer-Lock tip syringes due to demonstrated compatibility issues with certain infusion pump systems. The affected syringes may fail to function correctly with these pumps.
The FDA has recalled ION Sinus Spray due to microbial contamination of the non-sterile product. All lots are affected regardless of expiration date.
American Contract Systems is recalling CVS PCSU SJH IV catheter and adhesive components due to improper ethylene oxide sterilization. The components may have reduced functionality or elevated chemical residuals.
Smith & Nephew recalled 28 JOURNEY II knee prosthesis inserts because two different articular types were mislabeled and swapped during packaging. The incorrect labeling prevents identification of the actual insert type.
Carl Zeiss OPMI LUMERA 300 surgical microscopes may have a missing screw on the suspension arm, potentially allowing suspended components to fall and injure nearby persons. Eight units distributed in Maryland, Texas, California, Georgia, and Louisiana are affected.
American Contract Systems recalls cardiovascular surgical device components that were subjected to improper ethylene oxide sterilization at excessive temperatures, potentially causing loss of functionality or drug efficacy.
GE Healthcare's Universal Viewer Workflow Manager medical imaging software may show the wrong patient's information when third-party reporting applications are used. This data mismatch could cause confusion during medical procedures.
Mercedes-Benz is recalling 42,742 vehicles because they may lack a rear brake pad inspection gauge and manual instructions, potentially reducing braking ability.
American Contract Systems recalled General Pack medical device components (I.V. catheters and adhesive) that were improperly sterilized with ethylene oxide at higher than approved temperatures. The components may lack functionality or have elevated sterilization residuals.
The Maquet Acrobat-i Vacuum Stabilizer System's housing mount jaw may break during cardiac surgery, risking injury to heart tissue, blood vessels, or bypass grafts.