State
72,940 recalls have nationwide distribution and so reach Colorado. 6,941 additional recalls listed Colorado specifically in their distribution scope.
Of the 6,941 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 1,507 (22%) are Severe.
Which agencies issued them
These figures cover only the 6,941 recalls whose distribution notice names Colorado specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Micro Bird is recalling 2021-2026 G5, T-Series, and MB II school buses because a loose power cable connection may cause the air conditioning control board to overheat and melt, increasing the risk of a fire.
Micro Bird is recalling 2022-2026 G5 and T-Series transit buses because a loose power cable connection may cause the air conditioning control board to overheat and melt, increasing the risk of a fire.
About 210,000 INIU 10,000mAh power banks, model BI-B41, are being recalled after 15 reports of overheating including 11 fires, three minor burn injuries and over $380,000 in property damage.
Nova Bus is recalling certain water pumps because a loose impeller shaft may cause pump failure, increasing crash risk.
About 250 FUFU&GAGA queen size Murphy wall beds are being recalled after two reports of the 215-pound frame falling during assembly, injuring two consumers.
Motorcar Parts of America is recalling specific brake calipers for 2008-2025 Ford E-450 Super Duty vehicles because the piston bore wall may not meet specifications, causing the caliper to fracture.
About 3,170 Primark Water Balloon Pumps are being recalled because they can generate excessive pressure and rupture. Two US reports of cuts to hands and fingers have been received.
About 40 Cubimana treehouse building toy sets are being recalled because button cell batteries in the LED light piece can be easily accessed by children.
About 4,120 Casaottima 13-Drawer Dressers are being recalled because they are unstable when not anchored to a wall and violate the STURDY Act standard.
About 17,000 HydroJug 14-ounce children's sport tumblers are being recalled because the rivets on the handle can come loose, causing the handle to detach and posing a choking hazard.
About 300 Little Pea Shop padded crib bumpers are being recalled because they can obstruct an infant's breathing and are banned under the Safe Sleep for Babies Act.
About 9,400 CreateOn Crayola-branded pip-Cubes are being recalled because magnets can come loose if the seams separate, posing an ingestion hazard to children.
About 2,300 Grizzly Industrial 15-inch 3HP heavy-duty planers, model G0815, are being recalled because the chip breaker can contact the cutterhead blades and eject debris.
About 10,380 KTEBO writing tablet toys are being recalled because the screw securing the button cell battery compartment does not remain attached as the mandatory toy standard requires.
BMW is recalling 2026 X6, X7, X5, and X5 Plug-In Hybrid models. The instrument panel may prevent the passenger-side airbag from deploying properly during a crash.
Fresenius Kabi is recalling 2,199,850 vials of Famotidine Injection USP after out of limit results were obtained for endotoxin testing. The FDA classified it Class I.
Olympus is recalling 7,023 EVIS EXERA III TJF-Q190V duodenovideoscopes after continued reports of positive cultures and infections, and is updating the reprocessing materials.
Medtronic Sofamor Danek is recalling 275,260 Catalyft PL and PL40 expandable interbody spacers because the cage may lose height or collapse, risking migration or neurological injury.
Intelerad Medical Systems is recalling 19 IntelePACS InteleConnect and TechPortal installations because a bug can cause data loss in the Relevant Clinical Info field.
Volkswagen is recalling 27 vehicles with potentially incorrect wheel bolts that could detach during driving. Owners should not drive their vehicles until bolts are inspected and replaced by a dealer at no cost.
Stryker is recalling 39,148 NICO Myriad Illumination Packs because tape used to secure components in the packaging contains latex despite the products being labelled latex-free.
Medtronic MiniMed is recalling 12,126 CareLink Clinic installations because a software error displays incorrect data on the 24-hour sensor glucose overview graph.
Stryker is recalling 39,148 NICO BrainPath devices because tape used to secure components in the packaging contains latex despite the products being labelled latex-free.
Stryker is recalling 39,148 NICO Myriad Handpieces because tape used to secure components in the packaging contains latex despite the products being labelled latex-free.
Pivotal Health Solutions is recalling 34 Quantum Intersegmental Tables, model Q400, because damage to the heat function components can lead to overheating and smoldering.