Colorado recalls
1,962 federal recalls affecting Colorado in the last 12 months: 114 sold in Colorado plus 1,848 sold nationwide. From the CPSC, FDA, USDA and NHTSA.
Recent recalls
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Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker Sustainability Solution Color Cuff 18" (Red), Quick Connect Dual Port Single Bladder REF 5921-018-135 Stryker Sustainability Solution Color Cuff 18" (Red) Dual Port Single Bladder REF 5921-018-235.Sold nationwide. Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.
FDAApr 15, 2026Stryker
- MicroScan Neg Multidrug Resistant MIC 1 REF C32368 UDI-DI code: 15099590720568 Intended Use- For use with MicroScan Dried Gram Negative MIC/Combo Panels and Dried Gram Negative Breakpoint Combo Panels. MicroScan panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of aerobic and facultatively anaerobic gram-negative bacilli.
Sold nationwide. Due to manufacturing issue (incorrectly processing) with in vitro multidrug resistant test.
FDAApr 15, 2026Beckman Coulter
- Contact Spacelabs about your Model 91496 monitor
Sold nationwide. Certain Spacelabs Healthcare Model 91496 multi-parameter cardiac monitors have a circuit board defect. When the device is in Auto mode, the cardiac output measurement may start too early, causing errors that prevent proper readings or exclude readings that should be included. This could lead to inaccurate patient information and delayed medical decisions.
ModerateFDAApr 15, 2026Spacelabs Healthcare
- Cook Medical procedure kits recalled for expiration date errors
Sold nationwide. Cook Medical is recalling 18 product listings, including catheter, tracheostomy, and central venous kits and trays, because some affected lots were labeled with expiration dates longer than their true shelf life. No injuries have been reported, and the products were distributed worldwide.
ModerateFDAApr 15, 2026Cook18 products
- Stop using Molded Products MPC-130 Luer caps
Sold nationwide. Molded Products Inc. is recalling the MPC-130 See Luer Cap Set used in medical IV administration. The threaded sleeve can fail to engage properly, causing the cap to become detached during use. This affects 26,900 units distributed across Tennessee, Texas, Nevada, Illinois, and Florida.
ModerateFDAApr 15, 2026Molded Products
- Stop using Beckman Coulter MicroScan panels
Sold nationwide. Beckman Coulter identified a manufacturing defect in certain MicroScan Neg MIC 3J antibiotic susceptibility test panels (Catalog C54814, Lot 2025-08-23). Some panels are missing a drug in one well and contain double the amount of antibiotics in others, which could produce inaccurate test results. No injuries have been reported.
ModerateFDAApr 15, 2026Beckman Coulter
- Check Tornier HRS Max shoulder implant parts
Sold nationwide. Tornier, Inc. recalled three shoulder implant parts that were incorrectly labeled as compatible with the Tornier HRS Max system. These parts actually work only with the older Tornier HRS system and will not fit properly in HRS Max procedures. A total of 233 units with specific lot numbers were distributed nationwide.
ModerateFDAApr 15, 2026Tornier
- Medline NAMIC angiographic syringes recalled for disconnection risk
Sold nationwide. Medline is recalling 19 NAMIC angiographic syringes and Medline convenience kits that contain them. The syringe's rotating adaptor can unwind during use, which may loosen or fully disconnect the syringe from the manifold. No injuries have been reported.
SeriousFDAApr 15, 2026Medline19 products
- Contact Siemens about your ARTIS imaging system
Sold nationwide. Siemens ARTIS pheno and ARTIS Icono biplane imaging systems may occasionally display an incorrect, higher x-ray dose reading during patient exams. The actual radiation dose delivered is safe and meets regulatory standards, but the displayed reading can be misleading. This affects certain model numbers used in hospitals and imaging centers.
ModerateFDAApr 15, 2026Siemens
Vital Nutrients Aller-C recalled for undeclared egg, soy, hazelnutBlueroot Health, Inc. is recalling Vital Nutrients Aller-C vitamin supplements because they contain egg, soy, and hazelnut that are not listed on the label. This poses a serious risk to people with allergies to these ingredients. The recall affects 100-count and 200-count bottles distributed across the U.S.
SeriousFDAApr 15, 2026Vital Nutrients
Teva clonidine patches recalled for unapproved raw materialSold nationwide. Teva Pharmaceuticals is recalling certain Clonidine Transdermal System patches (0.1 mg/day) because they were manufactured using an unapproved raw material that does not meet FDA standards. The affected patches were distributed in the U.S. The company and FDA are working to ensure the product is removed from use.
ModerateFDAApr 15, 2026Teva3 products
- Check GE Healthcare Omnipaque injection lot numbers
Sold nationwide. GE Healthcare has recalled specific lots of Omnipaque (iohexol) injection, a contrast dye used in medical imaging, because some vials may contain visible particles. This could affect the safety of the procedure if the contaminated solution is used.
ModerateFDAApr 15, 2026GE Healthcare2 products
- Xanax XR 3 mg tablets recalled for failed dissolution
Sold nationwide. Viatris is recalling one lot of Xanax XR (alprazolam) 3 mg extended-release tablets because they failed to meet dissolution specifications—meaning the tablets may not break down and release the medication properly in your body. This affects only lot #8177156 with an expiration date of 02/28/2027, distributed nationwide. No injuries have been reported.
ModerateFDAApr 15, 2026Viatris
- Preferred Pharmaceuticals eye drops recalled for lack of sterility assurance
Sold nationwide. Preferred Pharmaceuticals' Artificial Tears Lubricant Eye Drops in 0.5 oz bottles may not be sterile due to a manufacturing issue. The FDA is recalling specific lots because sterility cannot be assured. No injuries have been reported.
ModerateFDAApr 15, 2026Preferred Pharmaceuticals
- Fagron IV norepinephrine and vancomycin bags recalled for sterility concerns
Sold nationwide. Fagron Compounding Services is recalling five premixed IV bags in 0.9% sodium chloride: norepinephrine bitartrate (16 mg and 32 mg per 250 mL) and vancomycin (1 g, 1.25 g and 1.5 g per 250 mL). The bags were made by Fagron Sterile Services in Wichita, Kansas, and sold nationwide, and the company cannot assure they are sterile. A blue break-off part on the administration port could also detach. No injuries have been reported.
SeriousFDAApr 15, 2026Fagron Compounding Services5 products
- Fresenius Kabi IV saline and dextrose bags recalled over sterility
Sold nationwide. Fresenius Kabi is recalling 14 sodium chloride and dextrose IV fluid bags because the company cannot assure they are sterile. The products were sold under the Fresenius Kabi, BD and Fresenius Medical Care names and were distributed nationwide, to Alaska and to Puerto Rico. No injuries have been reported.
ModerateFDAApr 15, 2026Fresenius Kabi14 products
- Cipla lanreotide injection recalled for sterility assurance concern
Sold nationwide. Cipla is recalling two versions of its lanreotide injection, 120 mg/0.5 mL pre-filled syringes, sold nationwide. The recall was prompted by an FDA observation at the contract manufacturing site about visual inspection procedures, so the product cannot be assured to be sterile. No injuries have been reported.
ModerateFDAApr 15, 2026Cipla2 products
Morovan nail polish remover recalled for methylene chlorideSold nationwide. Morovan gel nail polish remover (15ml bottle, turquoise with white cap) was found to contain methylene chloride and chloroform—chemicals prohibited in cosmetics. Methylene chloride may cause cancer and is not allowed in cosmetics at any level under FDA regulations. About 4,000 units were sold on Amazon between August 2025 and January 2026.
ModerateFDAApr 9, 2026
Muscccm pool drain covers recalled for entrapment and drowning riskSold nationwide. Muscccm-branded pool drain covers sold on Amazon do not meet federal safety standards for drain protection. These covers create a risk that swimmers could become trapped or drown. About 480 covers were sold between February and March 2026.
SeriousCPSCApr 9, 2026Fenle
Prestige Supernova and Typhoon lighters recalled for fire riskSold nationwide. Prestige Import Group is recalling about 4,300 Supernova and Typhoon brand butane lighters because they lack the required child-resistant safety mechanism. These lighters do not meet federal safety standards and pose a risk of fire and burn injuries, especially to children. No injuries have been reported.
SeriousCPSCApr 9, 2026Prestige Import
Happiness Light LED lights recalled for coin battery ingestion riskSold nationwide. Happiness Light LED lights sold on Amazon contain easy-to-access coin batteries that children can swallow. Ingesting these batteries can cause serious internal burns and death. The lights also lack required safety warnings.
SeriousCPSCApr 9, 2026Happiness Light
Shenzhen Shijingjie male-to-male extension cords recalled for electrocution riskSold nationwide. Shenzhen Shijingjie male-to-male extension cords (model RY-US-06 and RY_US-1.5) sold on Walmart.com have exposed live prongs that can cause electrocution. These cords are sometimes used to connect generators to home outlets during power outages, which can backfeed electricity into the home's wiring and create fire risk. Their short length also encourages generators to run near homes or indoors, risking carbon monoxide poisoning.
SeriousCPSCApr 9, 2026Segmart
VEEKTOMX mini power banks recalled for fire and burn hazardsSold nationwide. The lithium-ion battery in VEEKTOMX VT103 power banks can overheat and catch fire. The company has received three reports of fires causing minor property damage. The power banks were sold on Amazon between January and September 2024.
SeriousCPSCApr 9, 2026Segmart
ShymeryDirect LED lights recalled for button battery ingestion riskSold nationwide. ShymeryDirect LED lights contain easily accessible lithium coin batteries (CR2032) that children can swallow, causing serious internal burns or death. The lights lack required safety warnings and violate federal battery safety standards.
SeriousCPSCApr 9, 2026ShymeryDirect
Yeeluzan pool drain covers recalled for entrapment and drowning riskSold nationwide. Yeeluzan pool drain covers sold on Amazon do not meet federal safety standards and can trap swimmers underwater, creating a drowning risk. About 640 white plastic drain covers (8.7 inches diameter, sold in two-packs) were sold from May 2025 through March 2026.
SeriousCPSCApr 9, 2026Yeeluzan
Besslly pumpkin carving kits recalled for button battery riskSold nationwide. Halloween pumpkin carving kits sold on Amazon contain tea light candles with button cell batteries that children can easily remove and swallow. Swallowing these batteries can cause serious internal injuries, chemical burns, and death. The kits lack required safety warnings.
SeriousCPSCApr 9, 2026Besslly Store
Head ski boots recalled for fall injury riskSold nationwide. Head USA ski boots from 2015–2022 with fluorescent yellow shells or soles can deteriorate and break during use, creating a serious fall risk. The company has identified specific model numbers and article codes affected by this defect. No injuries have been reported, but the boots pose a hazard if worn.
ModerateCPSCApr 9, 2026Head
Member's Mark 7' pre-lit twinkling buck recalled for burn riskSold nationwide. The wires in this decorative light-up buck can be connected incorrectly at the factory, causing a resistor to overheat. This creates a risk of burns or fire. The company has received five reports of smoke and burning smells.
ModerateCPSCApr 9, 2026Seasonal Specialties
SCUBAPRO Monorail weight pockets recalled for drowning riskSold nationwide. The D-ring handle on SCUBAPRO Monorail Weight Pockets can detach during diving. If this happens, you won't be able to remove the weight pocket in an emergency to surface safely, creating a serious drowning risk. The company has received two reports of handles detaching, though no injuries have occurred yet.
SeriousCPSCApr 9, 2026SCUBAPRO
Maitys magnetic drinkware charms recalled for magnet ingestion riskSold nationwide. Maitys magnetic drinkware charms sold on Amazon contain loose magnets that can separate and be swallowed by children. High-powered magnets in the digestive system can attract each other or metal objects, causing serious internal injuries including intestinal perforation, blockage, and potentially death.
SeriousCPSCApr 9, 2026Maitys