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.
About 6,800 YITA 16-drawer dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children.
About 470 bottles of Lotus Joy Organic Sweet Birch Essential Oil are being recalled because the methyl salicylate they contain is not in child-resistant packaging.
About 3,500 Cobelae Busy Books for toddlers are being recalled because beads on page eight can loosen and detach, posing a choking hazard.
About 300 Semfri-branded children's multi-purpose helmets are being recalled because they do not comply with the mandatory safety standard for bicycle helmets.
Hyundai is recalling certain 2025-2026 IONIQ 5 and 2026 IONIQ 9 vehicles because the high voltage battery system may contain an improperly tightened bus bar, which can cause a short circuit.
Superfoods, Inc. is recalling 795,834 units of Live it Up brand Super Greens because the products may be contaminated with Salmonella Typhimurium.
Superfoods, Inc. is recalling Live it Up brand Super Greens powder, net weight 8.5oz, because the products may be contaminated with Salmonella Typhimurium.
SunMed Holdings is recalling 95,300 units of the Broselow Pediatric Emergency Rainbow Tape because the product contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.
SunMed Holdings is recalling 89 units of the Filled Broselow Organizer, model 7730IALS, because the product contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.
SunMed Holdings is recalling 20,583 units of the Broselow Pediatric Emergency Rainbow Tape, model 7700RE, because it contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.
Fontaine Modification is recalling certain 2024-2025 Freightliner Business Class M2 vehicles because the steering gearbox assembly may have been assembled with insufficient oil.
Prima Vera Nueva is recalling 16,790 packages (4 tamales per package) of Black Bean Bonanza Tamales with Black Beans over potential contamination with Listeria monocytogenes.
Gold Star Distribution is recalling feminine hygiene products over potential exposure of rodents and rodent activity in its distribution center.
Daimler Coaches is recalling 2026 Mercedes-Benz Tourrider buses because a faulty door valve may prevent doors from opening, delaying emergency evacuation.
About 700 Scepter B62 gas and oil combination fuel containers are being recalled because they lack flame mitigation devices and the spout is not child-resistant.
Baxter Healthcare is recalling 125,496 bottles of Sterile Water for Irrigation, 250 mL, after plastic particles from the bottle rim were observed floating in the solution.
Cardinal Health is updating the instructions for use on 1,169,726 chest drainage units to clarify that the intended patient population is adults 18 years and older.
Aju Pharm is recalling 2,569 AlternatiV+ Max Knotless Anchors after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Aju Pharm is recalling 600 units of the Genesis Screw-In Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Philips North America is recalling 1 unit of the Evolution Upgrade 3.0T MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Philips North America is recalling 1 unit of the Ingenia Ambition S because exported MR Elastography stiffness maps may show stiffness value errors.
Philips North America is recalling 31 units of the Ingenia Elition X MR system because exported MR Elastography stiffness maps may show stiffness value errors.
NIPRO Technical Services is recalling 499 units of Conductivity Standard Solution because a defect in the solution can cause meters to report incorrect conductivity values for dialysate.
LSL Healthcare is recalling 1,400 Central Line Dressing Kits because the BD ChloraPrep Triple Swabsticks inside exhibit an open seal on the applicator packaging.
Philips North America is recalling 10 units of the Ingenia 1.5T MR system because exported MR Elastography stiffness maps may show stiffness value errors.