Colorado recalls
1,988 federal recalls affecting Colorado in the last 12 months: 114 sold in Colorado plus 1,874 sold nationwide. From the CPSC, FDA, USDA and NHTSA.
Recent recalls
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SEGMART mini toddler trampolines recalled for strangulation riskSold nationwide. SEGMART mini trampolines sold with accessory kits (hammock, punching bag, hand rings, basketball board) pose a strangulation risk. Young children can become entangled in the straps, which can cause serious injury or death. One child has already suffered a rope burn injury to the neck from the hammock straps.
SeriousCPSCApr 16, 2026Segmart
Fun and Function swing frames recalled for fall hazardSold nationwide. Fun and Function's metal multi-point swing frames (model MW7661) can crack or break during use, causing children to fall. The company has received 10 reports of frames cracking or breaking, with two children sustaining bruises.
ModerateCPSCApr 16, 2026Fun and Function
Arch Studio tea kettles recalled for handle detachment burn riskSold nationwide. The handle on Macy's Arch Studio tea kettles can detach during use when the kettle is heated, which could cause serious burns. The stainless-steel kettles have a black handle and measure about 10.7 inches long with a 1.9-quart capacity. The brand name and model number "HJ10525" are marked on the underside.
SeriousCPSCApr 16, 2026Macy's
ATOYUS activity cubes recalled for choking hazardSold nationwide. ATOYUS wooden activity cubes sold on Amazon contain small parts that can detach, including xylophone screws, clock hands, and mallet ends. These parts pose a choking risk for young children. The toys were sold between January and February 2026.
SeriousCPSCApr 16, 2026Melofaver US
nvyue Magic Pocket Staffs recalled for projectile riskSold nationwide. The protective pin on nvyue Magic Pocket Staffs can fail, causing the staff to expand suddenly without warning. This rapid expansion poses serious risks of eye injuries, lacerations, and cuts to the face and hands. CPSC has received 163 injury reports, including corneal lacerations and injuries requiring stitches, many involving children.
SeriousCPSCApr 16, 2026Xingwenfeng
Sanlebi Pet Vet playsets recalled for button battery riskSold nationwide. The Sanlebi Pet Vet Playset (model MX094) contains button cell batteries in the toy nail grinder and otoscope that children can easily access. Button cell batteries can cause serious injury or death if swallowed. About 4,650 playsets were sold on Amazon between June 2025 and January 2026.
SeriousCPSCApr 16, 2026Letokids
Generac portable generators recalled for fire and burn riskSold nationwide. Certain Generac portable generators can leak gasoline from the carburetor when first filled with fuel, creating a serious risk of fire or burns. The recall affects specific models sold between May 2025 and February 2026. No injuries have been reported so far.
SeriousCPSCApr 16, 2026Generac
BATOYAK USA pressure washers recalled for electrocution riskSold nationwide. BAYOTAK USA-branded electric pressure washers (model C4012PLUS-1500C) lack a required ground-fault circuit-interrupter (GFCI) safety device. This missing protection creates a serious risk of electric shock or electrocution during use. About 360 units were sold online between October 2025 and January 2026.
SeriousCPSCApr 16, 2026BAYOTAK USA
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