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.
Superbobi 7 3/8-inch pool drain covers violate federal safety standards and pose entrapment and drowning hazards. Pool owners should stop using affected covers immediately.
Amazon is recalling Amazon Basics 55 Lbs. Adjustable Dumbbells because weight plates can fail to engage completely and dislodge during use, posing an impact hazard. No injuries have been reported.
Cook Incorporated is recalling Aurous Centimeter Sizing Catheters due to risk of marker band cracking or breakage during angiographic procedures. Potential complications include device fragmentation, vessel injury, and in worst-case scenarios, life-threatening harm or death.
Cook Incorporated is recalling Centimeter Sizing Catheters because marker bands may crack or break, potentially causing device fragmentation, vessel injury, or life-threatening harm.
Medline Industries is recalling multiple surgical convenience kits because equipment used to sterilize and package the devices had calibration issues that may have affected sterility assurance. The devices were processed through validated sterilization cycles but the calibration problems could impact their sterility.
Cook Incorporated is recalling Beacon Tip Centimeter Sizing Catheters because marker bands may crack or break, which could lead to device fragmentation, prolonged procedures, vessel injury, and in worst-case scenarios, life-threatening harm or death.
Acella Pharmaceuticals is recalling Naproxen oral suspension due to the presence of lead and lithium above specification levels. The recall affects 6,336 bottles distributed nationwide.
Raw Farm Original Raw Cheddar in 80 oz bulk format is being recalled in connection with a multi-state outbreak of E. coli O157:H7.
Medline Industries is recalling multiple convenience kit models due to calibration issues with equipment used to sterilize and package the devices, which could affect sterility assurance levels.
Milk Wash packed exclusively for Chick-fil-A is being recalled after the firm's supplier reported that the nonfat dry milk may be contaminated with Salmonella.
French Broad Chocolate bette's bake sale bonbon assortments are being recalled because the printed tasting guide misidentifies the Walnut Fudge and Peach Cobbler chocolates.
Milk-N-Egg Mix in 50 lb bags is being recalled after the firm was notified by its supplier that the nonfat dry milk may be contaminated with Salmonella. 833 bags are affected.
Raw Farm Raw Cheddar Original in 8 oz and 16 oz sizes is being recalled in connection with a multi-state outbreak of E. coli O157:H7.
B. Braun Medical Inc. is recalling Lactated Ringer's Injection USP (1000 mL containers) due to the presence of particulate matter. The recall affects 95,412 containers distributed nationwide.
Raw Farm Shredded Raw Cheddar in 80 oz bulk format is being recalled in connection with a multi-state outbreak of E. coli O157:H7.
Lucid is recalling certain 2024-2025 Air rear-wheel drive vehicles because the Gen 4 inverter may experience internal friction and become damaged, causing a loss of drive power.
Erbe Medical is recalling ERBEFLO CleverCap CO2 hybrid tubing and cap sets used with endoscopes because the distal connector may allow unintended water flow, potentially leading to water aspiration and serious respiratory complications.
Medline Industries is recalling approximately 29,192 labor and delivery kits and OB packs due to calibration issues in sterilization equipment that may impact sterility assurance. The products were exposed to validated sterilization cycles, but the calibration problems potentially compromise sterile status.
Teva Pharmaceuticals USA, Inc. is recalling 2,200 kits of Octreotide Acetate for Injectable Suspension (30 mg) due to quality system deficiencies that affect sterility assurance. The recall affects all lots nationwide.
Medline is recalling multiple convenience kits used in catheterization labs and surgical procedures due to calibration issues with sterilization equipment that may affect sterility assurance. The affected kits were distributed nationwide.
Medline Industries is recalling six models of medical device convenience kits due to calibration issues with sterilization and packaging equipment that may have reduced sterility assurance levels. The recall affects 553 units distributed nationwide.
Medline Industries is recalling four Convenience Kit models (892 units) nationwide because sterilization and packaging equipment calibration issues may have compromised the sterility assurance level of the devices.
Fresenius Medical Care is recalling DELFLEX Dextrose Peritoneal Dialysis Solution bags due to potential leaks from bag perforations that could compromise sterility. Affected patients should contact their healthcare provider immediately.
Meatloaf seasoning packed for the Costco service deli is being recalled after the firm's supplier reported that the nonfat dry milk may be contaminated with Salmonella.
CareFusion 213, LLC is recalling BD PurPrep (povidone-iodine 8.3% with isopropyl alcohol 72.5%) due to lack of assurance of sterility and potential product contamination. Affected lots are distributed nationwide.