State
72,907 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 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The MOSAIQ Oncology Information System is being recalled because the software may fail to load an adapted baseline shift plan during treatment delivery when a communication error occurs.
MIC Safety PEG Kits with ENFit Connectors, 24 Fr PULL, catalog number 8180-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.
CORFLO Safety PEG Kits with ENFit Connector, catalog number 50-6312, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 43 kits affected.
Dragonfly Thai Ginger Powder, 4.37 oz, packed for U.S. Trading Company, is being recalled over potential contamination with lead. 1,800 units are affected.
MIC Safety PEG Kits, 20 Fr PULL, catalog number 7180-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 3,184 kits affected.
TDC VELOCE 25G Two Dimensional Cutters are being recalled following an increase in complaints of a loose outer knife, including reports of it loosening during use.
The SporeTraq Mail-In Spore Testing Service, 52 tests, is being recalled because an incorrect incubation process was performed on the product. 2,210 units are affected.
EXCOR Pediatric VAD System blood pump PU valves are being recalled because the inner package expiration date does not match the correct outer package date.
Boston Scientific CSK stainless steel electrodes across several lengths are being recalled because the reusable electrodes may not meet expected performance levels. 31,923 units affected.
The SporeTraq Mail-In Spore Testing Service, 12 tests, is being recalled because an incorrect incubation process was performed on the product.
NeoSpan SuperElastic Compression Staple kits are being recalled because the Magnetic Resonance Conditional symbol is missing from the carton, inner tray and patient label. 306 kits affected.
Boston Scientific TCN nitinol electrodes across four lengths are being recalled because the reusable electrodes may not meet expected performance levels. 49,251 units affected.
Minocycline Hydrochloride Extended-Release Tablets, USP, 115 mg, are being recalled after an out-of-specification dissolution result at the ninth month of testing. 360 bottles affected.
Primidone Tablets, USP, 50 mg, from Amneal are being recalled over the potential for cross-contamination with acemetacin API due to an issue at the API manufacturer. 27,936 bottles affected.
Epinephrine Injection, USP, 1 mg/mL single-dose vials from Fresenius Kabi are being recalled because they failed impurities and degradation specifications. 898,050 vials affected.
Neuro Nourish, a 6-in-1 nutritional supplement, is being recalled because premature lipid oxidation may give the product an off odor and bitter taste. 512 units affected.
Mahurkar Elite PASS Trays are being recalled because the Tegaderm CHG dressing specified in the product labeling was missing from certain lots. 25,627 units are affected.
Storyteller Overland is recalling 2024-2026 GXV Hilt vehicles because a secondary alternator pulley may fail, causing loss of power brakes and steering.
Forest River is recalling 2023-2024 XLR Toy Hauler trailers because the listed Gross Vehicle Weight Rating exceeds the chassis rating, creating a risk of overloading and crashes.
Wabash is recalling 2027 van trailers because improperly tightened bumper tube bolts may reduce rear impact guard protection, increasing injury risk in crashes.
Daimler Trucks North America is recalling 2027 Thomas Built SAF-T-LINER HDX2 school buses because front and mid-body interior joints may have insufficient strength, increasing injury risk in a crash.
Waymo is recalling 5th Generation Automated Driving Systems because software may allow vehicles to enter closed freeway construction zones, increasing crash risk.
Altec is recalling 2014-2026 AT Series aerial vehicles because a missing transmission interlock may allow the aerial device to operate while the chassis is not in park.
Marion Body Works is recalling Waltco MDV series liftgates on Morgan aluminum dry vans because deck pins may break, causing the platform to fall.
Winnebago is recalling 2026-2027 Revel and Revel Sport vehicles because the tire information label lists the wrong tire size, which could lead to incorrect replacements and increased crash risk.