State
72,913 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 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Thermos Stainless King food jars and Sportsman bottles are recalled after 27 reports of stoppers ejecting forcefully on opening, including three consumers with permanent vision loss.
Stephan Baby Boo Bunnie and Friends toys are recalled after 20 reports of the water-filled cube cracking or breaking, including one case where a child swallowed sharp pieces.
Honda is recalling model year 2025-2026 CRF250R and CRF450R off-road motorcycles because the handlebar clamp can allow the handlebar to rotate unexpectedly. One crash reported.
Nova Bus is recalling certain 2022-2023 LFS transit buses because a telemetry control unit may cause a data overload, shutting down the unit and causing a loss of drive power.
Malker Bicycle Light Sets are recalled because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. About 7,000 units are affected.
USDA FSIS issued a public health alert for meat and poultry products containing FDA-regulated dairy ingredients that may be contaminated with Salmonella. No illnesses have been reported to date.
Acer AES015 folding electric scooters are recalled because a loose screw can cause the front tube to fold down unexpectedly, posing a fall hazard. About 510 US units are affected.
Build-A-Bear Workshop Heartwarming Hugs Bears are recalled because the zipper slider on the side pouch can detach, posing a choking hazard to children. About 36,000 units are affected.
Hepo adult portable bed rails are recalled because users can become entrapped within the rail or between the rail and the mattress. About 2,200 units are affected.
UHOMEPRO 5-Drawer Dressers are recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children. About 5,190 units are affected.
StrikeLock hoistway door locking devices for residential elevators are recalled because they can allow the elevator cab to move with a landing door open, posing a fall hazard.
Earthtec 7 3/8 inch pool drain covers are recalled because they violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act.
1-K Kerosene Heater Fuel portable containers are recalled because they lack the flame mitigation devices required under the Portable Fuel Container Safety Act. About 30,155 units are affected.
Travel Size Afrin Original Nasal Spray 6 mL bottles are recalled because the packaging does not meet Poison Prevention Packaging Act requirements for imidazolines.
Segmart 4-Drawer Dressers are recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children. About 16,440 units are affected.
Qumeney Bicycle Light Sets are recalled because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. About 2,800 units are affected.
DGIVOVO US electric pressure washers are recalled because they lack an integral ground-fault circuit interrupter, posing shock and electrocution hazards. 50 units are affected.
Medline Industries has recalled its PICC Tray (Model DYNJ41648A) because the 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded by FDA.
Medline Industries is recalling certain Labor Pack kits (Model DYNJ44813D) nationwide because their 510(k) regulatory clearances for Control Syringes, Guidewires, and High-Pressure Tubing have been rescinded.
Angiodynamics, Inc. is recalling Soft-Vu Angiographic Catheter (Straight Art, Non-Braided) units due to a manufacturing defect that may prevent guidewires from passing through the catheter hub's inner diameter.
Medline Industries is recalling Convenience Kits containing 10mL Polycarbonate Colored Syringes due to unapproved design changes made outside of FDA 510(k) clearance. The recall affects multiple product SKUs distributed nationwide and internationally.
Medline Industries is recalling 41 different surgical kit models nationwide because regulatory clearances for certain control syringes, guidewires, and high-pressure tubing have been rescinded. Affected facilities should stop use and contact Medline.
Dorman is recalling specific transmission gearshift cables where the bushing may detach, preventing the vehicle from shifting into Park and increasing the risk of a crash.
Kirkland Signature Traditional Madeleines are being recalled because packages were filled with heart madeleines containing undeclared hazelnut and soy lecithin. 92 units are affected.
Medline Industries is recalling multiple Convenience Kits containing 10mL Polycarbonate Colored Syringes due to unapproved design changes made outside of FDA 510(k) clearance. The recall affects products distributed worldwide including the US, Canada, Panama, and Barbados.