Colorado recalls

Sold nationwide. COMMOWNER 3 GPM electric pressure washers lack proper electrical safety protection and have a short power cord that encourages unsafe extension cord use. This creates a serious risk of electric shock or electrocution.

Serious·CPSC·Aug 13, 2026·AZ Home Concept

Sold nationwide. Deli-branded fuel containers sold on Walmart.com have closures that are not child-resistant, which violates federal safety requirements. Children could open the containers and be exposed to fuel, risking serious burns, poisoning, or other injury.

Serious·CPSC·Aug 13, 2026·Deli OfficeSupplies

Sold nationwide. DUMOS Nine-Drawer Fabric Dressers can tip over and trap children if not anchored to the wall. These dressers were sold online as television stand furniture and do not meet federal safety standards for clothing storage units. About 8,981 units were sold.

Serious·CPSC·Aug 13, 2026·Jiayubo

Sold nationwide. TooyBing wooden bead stacking toys intended for children under 3 years old contain small wooden beads that pose a serious choking hazard. These toys violate federal small parts regulations designed to protect infants and toddlers.

Serious·CPSC·Aug 13, 2026·Guangzhou Yide Toys

Sold nationwide. Taleco Gear baby jumpers, swings, and 2-in-1 jumper & swing products can become unstable, creating a fall and impact hazard. The hanging restraint straps and seat openings also pose a strangulation risk. The company has received at least 52 reports of these hazards, including 32 reports of injuries such as head bumps.

Serious·CPSC·Aug 13, 2026·Taleco Gear

Sold nationwide. Brookstone-branded Tabletop Fire Pits can cause uncontrolled fires where flames spread across spilled alcohol and shoot out from fuel containers, causing serious or fatal burns. Southern Telecom has received two reports of flame jetting that resulted in second- and third-degree burns.

Serious·CPSC·Aug 13, 2026·Southern Telecom

Sold nationwide. Goody King magnetic building cubes contain magnets that can come loose if the cubes break or open. If a child swallows these loose magnets, they can attract each other inside the digestive system and cause serious injury, including intestinal perforation, blockage, or death.

Serious·CPSC·Aug 13, 2026·Iceberg

Sold nationwide. The electrical switch in certain Cooluli minifridges can short circuit, creating a fire and burn risk. The company has received reports of units smoking, sparking, catching fire, and overheating, with one person injured by smoke inhalation.

Serious·CPSC·Aug 13, 2026·Iceberg

Sold nationwide. The Neuroguard IEP carotid stent and post-dilation balloon system has an integrated filter that may fail to open after the sheath is retracted, due to a wire-to-filter bond issue. If this happens during a procedure, the device may lose its intended embolic protection. No injuries have been reported.

Moderate·FDA·Aug 12, 2026·Contego Medical

Sold nationwide. Freudenberg Medical is recalling two Blom-Singer Classic Indwelling Voice Prosthesis products (16Fr/10 mm, REF 1610-LEF and 1610-LF) because the boxes are labeled incorrectly. The box labeled for one product holds the other, so the product inside may not match the label. The recall covers 52 units and was distributed nationwide in the US and to the UK and France. No injuries have been reported.

Moderate·FDA·Aug 12, 2026·Freudenberg Medical2 products

Sold nationwide. The 36-month shelf life on COAPTIUM Connect peripheral nerve repair devices is not substantiated by real-time data, so devices will be relabeled with a 26-month shelf life. Using a device past its validated shelf life may cause it to break during surgery and become unusable; the worst-case outcome would be revision surgery. No injuries have been reported.

Moderate·FDA·Aug 12, 2026·Tissium7 products

Sold nationwide. Instrumentation Laboratory is recalling 141 units of two blood analysis systems: 32 GEM Premier 7000 with iQM3 units and 109 GEM Premier 5000 PAK units. The active ingredient concentration in the lysing bag solution did not meet manufacturing specifications, which could delay recognition and management of co-oximetry and total bilirubin abnormalities. The FDA classified it as Class II, and no injuries have been reported.

Moderate·FDA·Aug 12, 2026·Instrumentation Laboratory2 products

Sold nationwide. United Orthopedic Corp. is recalling three femoral offset bushings (0mm and 4mm, catalog 9323-5310, lot 25FC58) from its U2 Total Knee System. The implant's engraved numbering may be incorrect, which could lead to it being placed in the wrong orientation. The units were distributed in Texas and Michigan, and no injuries have been reported.

Moderate·FDA·Aug 12, 2026·United Orthopedic2 products

Sold nationwide. Aniara Diagnostica LLC is recalling its 5-PLASMA Bivalirudin AMR Verification Kit because stability issues were found with the reconstituted lyophilized human plasma and bivalirudin matrix. These issues cause measurable bivalirudin to degrade in the controls, calibrators, and linearity values. The kit was distributed in IL, NC, and TN, with no injuries reported.

Moderate·FDA·Aug 12, 2026·Aniara Diagnostica3 products

Sold nationwide. Philips is recalling 3 interventional X-ray system lines, sold as Philips Allura (including Allura Xper FD10 and Allura Centron), Philips Azurion, and Allura Centron, with about 8,610 units affected. The systems may contain unauthorized hard disk drives, which could cause loss of imaging, loss of motorized movement, or loss of data. No injuries have been reported.

Moderate·FDA·Aug 12, 2026·Philips3 products

Sold nationwide. Siemens Healthcare Diagnostics is recalling the Atellica CH Urine Albumin test (REF 11537225) used on CI analyzers. The test may produce falsely low urea nitrogen and hemoglobin A1c results, and may cause more quality control failures that delay results.

Moderate·FDA·Aug 12, 2026·Siemens

Sold nationwide. Beckman Coulter is recalling two MicroScan LabPro V5.03 Panel Update 11 products, an electronic update (REF D23352) and a DVD kit (REF D23354), for installation on MicroScan instruments such as the autoSCAN-4 and WalkAway-40 plus. The analyzers contain incorrect algorithms that may affect antimicrobial susceptibility test results and lead to false susceptibility classifications. The recall covers products distributed nationwide, including the listed states.

Moderate·FDA·Aug 12, 2026·Beckman Coulter2 products

Sold nationwide. Hardy Diagnostics is recalling HardyDisk AST Cefiderocol 30 µg (catalog Z9435) because incorrect cartridges were included in some units. This may lead to false-susceptible or false-resistant results, which could result in an ineffective antimicrobial being chosen. No injuries have been reported.

Moderate·FDA·Aug 12, 2026·Hardy Diagnostics

Sold nationwide. United Orthopedic is recalling four surgical knee instrument products, including U2 Total Knee System PSA box trials and femoral valgus adaptors, and USTAR II Knee System hinge box trials. An incomplete process on a component screw made by a subcontractor prevents the instruments from being assembled properly. The products were distributed nationwide, with distribution in Texas and Michigan. The notice reports no injuries.

Moderate·FDA·Aug 12, 2026·United Orthopedic4 products

Sold nationwide. Happiest Baby, Inc. is recalling refurbished pre-loved SNOO Smart Sleeper bassinets that failed to meet quality standards before they were distributed. The recall is being reported retroactively. The units were distributed in PA, WA, CA, and NJ, and 4 units are affected. No injuries have been reported.

Moderate·FDA·Aug 12, 2026·Happiest Baby

Sold nationwide. Siemens Healthcare Diagnostics recalled Lot U2 of its Syva Emit tox Serum Tricyclic Antidepressant Calibrator/Controls because the sodium azide concentration is outside specifications. The company says assay results were not affected, and the health risk to lab technicians is low, with the worst expected outcome being mild skin or eye irritation.

FDA·Aug 12, 2026·Siemens

Sold nationwide. Lot U1 of the Syva Emit Disopyramide Enzyme Immunoassay calibrator has an out-of-specification sodium azide concentration. The notice says assay results were not affected, and the health risk to lab technicians is low, with the worst outcome being mild skin or eye irritation. No injuries have been reported.

FDA·Aug 12, 2026·Siemens

Sold nationwide. GE Healthcare is recalling Portrait Core Services software version 1.2.0 because a software vulnerability may allow unauthorized persons to gain privileged access to the device. This could result in loss of patient monitoring, missed patient alarms, or access to protected health information. No injuries have been reported.

Moderate·FDA·Aug 12, 2026·GE

Sold nationwide. Biofire Defense is recalling 122 kits (3,660 pouches) of the FilmArray NGDS Warrior Panel, a test that detects several dangerous pathogens in human whole blood. The firm found mismatches between the outbreak strain and the reference strain used to develop the test. The notice reports no injuries.

Moderate·FDA·Aug 12, 2026·Biofire Defense

Sold nationwide. GE Healthcare recalled certain MAC VU360 electrocardiograph units running software v3.0. After the order refresh icon is selected, a preview or review screen may not close automatically after 2 minutes of inactivity, so data from a previous patient could stay on screen and be linked to the next patient. No injuries have been reported.

Moderate·FDA·Aug 12, 2026·GE

Sold nationwide. Merge Healthcare is recalling 58 imaging workstations in two products: 53 units of Merge PACS and 5 units of Merge OrthoPACS. Thumbnails from a previously opened patient study may appear in the Thumbnail Bar while a different patient study is open. The FDA classified the recall as Class II. The notice reports no injuries. It covers US nationwide distribution and Canada and the UK.

Moderate·FDA·Aug 12, 2026·Merge Healthcare2 products

Sold nationwide. Zimmer Biomet is removing certain sizes of its Intramedullary Bone Saw Blade Assembly from use. The recall is due to potential damage to the sterile barrier packaging, which could leave the saw blade exposed. The notice reports no injuries.

Moderate·FDA·Aug 12, 2026·Biomet5 products

Sold nationwide. Stryker is recalling three tube set products: the AHTO Tube Set, the AHTO Dual Spike Tube Set and the Single Spike Tube Set. The FDA reports an increase in complaints describing leaking from the handpiece during use. The products were distributed in the US and in 17 other countries, and no injuries have been reported.

Moderate·FDA·Aug 12, 2026·Stryker3 products

Sold nationwide. Nuclein LLC is recalling the DASH Rapid PCR Instrument, model SG-0002 running software 6.0.2, because a software issue may produce false co-infection results, such as a positive for Flu A when SARS-CoV-2 is present. Two units were affected, and no injuries have been reported. The FDA has classified this as a Class II recall.

Moderate·FDA·Aug 12, 2026·Nuclein

Sold nationwide. Maquet Critical Care AB recalled certain Flow-i, Flow-c and Flow-e anesthesia machines after events were observed in which anesthetic agent was not delivered when the vaporizer was activated. The agency says this failure may result in a patient receiving insufficient anesthesia and may lead to intraoperative awareness. No injuries have been reported.

Moderate·FDA·Aug 12, 2026·Maquet