State
73,738 recalls have nationwide distribution and so reach Colorado. 6,951 additional recalls listed Colorado specifically in their distribution scope.
Of the 6,951 recalls naming Colorado we have scored against our rubric, 1,215 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,826 (26%) are Severe.
Which agencies issued them
These figures cover only the 6,951 recalls whose distribution notice names Colorado specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Breez 2-in-1 Smart Bedroom Fan and White Noise Machines are recalled because the internal power connector can corrode and cause the fan to overheat, posing a fire risk.
Yeeluzan pool drain covers are recalled because they violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act, posing entrapment and drowning hazards.
Iron-containing dietary supplements from eleven brands are recalled because their packaging is not child-resistant as required by the Poison Prevention Packaging Act. About 356,140 units are affected.
Silks-branded children's loungewear sets are recalled because they violate mandatory flammability standards for children's sleepwear. About 7,900 units are affected.
Happiness Light LED lights are recalled because their lithium coin batteries can be accessed easily by children, posing an ingestion hazard. About 2,800 units are affected.
Akron Brass is recalling Enovation Controls PowerView 700 displays that may fail to power on or respond to touch, preventing the activation of emergency lights and equipment.
Maitys drinkware charms are recalled because they contain loose magnets that violate the mandatory magnet standard, posing an ingestion hazard to children. About 16,400 units are affected.
The Member's Mark 7-foot Pre-Lit Twinkling Buck is recalled because the current limiting resistor can overheat if the wires are connected incorrectly, posing a burn hazard. About 2,460 units are affected.
Chrysler is recalling certain 2026 Jeep Cherokee vehicles because the brake system control module may fail, causing loss of anti-lock brakes (ABS) and electronic stability control (ESC), which increases crash risk.
SCUBAPRO Monorail Weight Pockets are recalled because the D-ring handle used to release the pocket from a buoyancy compensator can detach, preventing weight ditching in an emergency.
Besslly Halloween Pumpkin Carving Kits are recalled because children can easily access the button cell batteries in the included tea lights, posing an ingestion hazard. About 650 units are affected.
Chrysler is recalling 2026 Jeep Wrangler vehicles because insufficient child seat tether welds may reduce restraint effectiveness during a crash.
Philips Respironics is recalling the Trilogy Evo O2 ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Philips Respironics is recalling the Trilogy Evo Universal ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Philips Respironics is recalling the Trilogy Evo ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
One lot of Magnesium Sulfate in Water for Injection is being recalled after a foil pouch labeled as magnesium sulfate was found to contain an IV bag of tranexamic acid.
Imu-Tek Animal Health has recalled Imu-Tek Colostrum-5 Powder because the product may be under-processed. The recalled lot was distributed across 29 states.
Philips Respironics is recalling the Trilogy EV300 ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Philips is recalling the Azurion 5 M12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
The 2.4 VOLT Tap Locking Screw Tap is being recalled after a full lot swap with the Cortical Screw Tap left the bone taps with an incorrect thread.
Medline is recalling kits containing ENFit G-tube connectors because the connectors were not made to required dimensional specifications and may not form a proper seal.
Medline is recalling BAL and ENDO kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Medtronic is recalling MiniMed 620G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Philips is recalling the Allura Xper FD20/10 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Toyota is recalling specific Lexus RC, GS, and IS models because a failing fuel pump can cause the engine to stall, increasing crash risk.