FDA•MODERATE
Halyard LAVH Pack Clearify Visualization System
AVID Medical recalls Halyard LAVH Pack (USAR053-11) due to possible leakage of the Clearify Visualization System.
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FDA•MODERATEGetinge SERVO-U/SERVO-N Y Sensor ModuleGetinge recalls SERVO-U/N Y sensor module over missing safety electrical testing.
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FDA•MODERATEOverStitch Suture CinchBoston Scientific recalls OverStitch Suture Cinch over deployment and suture-cutting failures.
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FDA•MODERATETD Navio Midi Speech Generating DeviceTobii Dynavox recalls TD Navio Midi speech device over battery tab damage risk.
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Kico Knee recalls ARVIS Surgical Navigation System Gen 2 over tilted eyepiece image from sensor issue.
2 products 
FDA•MODERATEPhilips Cardiac Workstation 5000Philips recalls Cardiac Workstation 5000 over intermittent inaccurate heart-rate data.
2 products
FDA•MODERATEDentsply Sirona Capsule MixerDentsply Sirona Capsule Mixer recalled over electrical discharge risk when unplugged.
FDA•MODERATEIntersurgical One-Piece Guedel AirwayIntersurgical recalls One-Piece Guedel Airway, size 00, ISO 5.0, Blue, due to potential occlusion.
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Foundation Medicine recalls Hamilton Microlab STAR PCT v2.0.0 over spontaneous software closures.
FDA•MODERATEEndoFLIP 1 SystemCovidien recalls EndoFLIP 1 System due to 24-hour limit flagging products as expired.
2 products
NHTSA•MODERATEHorton Ambulance Touchscreen DisplayHalcore recalls 2025-2026 Horton ambulances over touchscreen failure that can disable emergency lights and equipment.
CPSC•COMMOWNER Pressure WashersCOMMOWNER pressure washers recalled over shock/electrocution risk due to missing GFCI and short cord.
CPSC•Cooluli MinifridgesCooluli recalls 10L and 15L minifridges due to fire and burn hazard from electrical switch short circuit.
CPSC•CuberShop Magnetic Speed CubesCuberShop Magnetic Speed Cubes recalled due to loose high-powered magnets posing ingestion hazard.
CPSC•Deli Fuel ContainersDeli fuel containers recalled; non-child-resistant closures pose burn and poisoning risks to children.
CPSC•DUMOS Nine-Drawer DressersDUMOS Nine-Drawer Dressers recalled due to tip-over and entrapment hazards; violate STURDY Act.
CPSC•Zimtown Portable Gas and Fuel CansZimtown 5-gallon gas cans recalled because non-child-resistant closures pose burn and poisoning risks.
CPSC•Merax Murphy BedsGigaCloud Technology (USA) Inc. is recalling Merax full-size and twin-size wall-mounted Murphy beds due to a frame that can fall onto consumers during assembly or disassembly, posing impact, crush, and laceration hazards.
CPSC•Goody King Magnetic Building CubesYi Suen Commerce recalls Goody King Magnetic Building Cubes over magnet ingestion hazard; full model list on CPSC page.
CPSC•Hampton Bay Halwin 52-Inch Ceiling FansHampton Bay Halwin 52-inch ceiling fans recalled due to blade separation hazard.
CPSC•Qabefy MattressesQabefy 10-inch twin mattresses recalled for violating flammability standard, posing fire risk.
CPSC•Ritchey Carbon Bicycle ForksRitchey recalls carbon bicycle forks due to loose alloy insert posing fall and crash hazard.
CPSC•Shengsen Prank Sound MakersShengsen Prank Sound Makers recalled due to accessible coin batteries posing ingestion hazard.
CPSC•Brookstone Tabletop Fire PitsBrookstone tabletop fire pits recalled due to burn and fire hazards.
CPSC•SUGIFT Pressure WashersSUGIFT recalls 2.8 GPM electric pressure washers (model LTBBHG006) over shock and electrocution hazards from missing GFCI.
CPSC•Taleco Gear Baby Jumpers and SwingsTaleco Gear recalls baby jumpers and swings due to fall, impact, and strangulation hazards.
CPSC•TooyBing Wooden Bead Stacking ToysTooyBing Wooden Bead Stacking Toys recalled due to choking hazard; sold on Amazon.
CPSC•Yamazuki Youth ATVsYamazuki recalls QEASET/HOVERHEART youth ATVs (model XW-A19) over brake, speed limiter, and reflector defects posing crash hazard.
FDA•MODERATEShoolin Pharma Chem: multiple drugsShoolin Pharma Chem recalls Sildenafil and Tadalafil APIs due to CGMP deviations.
5 products
FDA•MODERATEClear Eyes Maximum Itchy Eye ReliefClear Eyes Maximum Itchy Eye Relief recalled over potential sterility issues.
FDA•MODERATEPresource KitsCardinal Health is recalling multiple Presource procedural kits due to possible endotoxin contamination.
13 products
NHTSA•MODERATEFord Explorer Engine Rod BearingFord recalls 2026 Explorer 2.3L engines over rod bearing seizure risk.
NHTSA•MODERATEChevrolet Silverado 2500 / GMC Sierra 2500 Tire Pressure LabelGM recalls 2024-2025 Silverado 2500 and Sierra 2500 with 20-inch accessory wheels over incorrect tire pressure label.
2 products
NHTSA•MODERATEJeep Grand Cherokee Windshield WipersChrysler recalls 2026 Jeep Grand Cherokee and Grand Cherokee L over wiper failure risk.
NHTSA•MODERATEDodge Durango Rear SpoilerChrysler recalls 2021-2023 Dodge Durango rear spoilers that may detach, posing a crash risk.
NHTSA•MODERATERange Rover Front Suspension KnucklesLand Rover recalls 2016-2017 Range Rovers over incorrect front suspension knuckles that may cause loss of control.
NHTSA•MODERATENissan Altima Front Passenger Air BagsNissan recalls 2025 Altima over front air bags that may not deploy due to incorrect mounting fasteners.
NHTSA•MODERATEChrysler Rearview CameraChrysler recalls certain 2026-2027 Jeep, Ram, Chrysler, and Dodge vehicles over rearview camera display failure.
FDA•MODERATEERBECRYO 2 Cryosurgical UnitErbe USA recalls ERBECRYO 2 Cryosurgical Unit (Model 10402-000) over risk of cryoprobe rupture from CO2 leak.
FDA•MODERATEBIOFIRE Respiratory Panel 2.1BioFire recalls BIOFIRE Respiratory Panel 2.1 over increased false negatives.
NHTSA•MODERATEBMW Driveshaft ConnectionBMW recalls certain 840i, 540i, M550i, and 750e xDrive models over driveshaft damage that can cause loss of power or rollaway.
NHTSA•MODERATEBMW X3 Steering SpindleBMW is recalling certain 2024-2026 X3 vehicles over a steering spindle that may be incorrectly attached, risking loss of steering control.
NHTSA•MODERATEGrote Replacement Marker LightsMack Trucks recalls Grote replacement marker lights (PN 78513681) that may fail to illuminate, increasing crash risk.
2 products
NHTSA•MODERATEGrote Marker LightsVolvo recalls Grote marker lights (PN 78513681) that may fail to illuminate, increasing crash risk.
2 products
NHTSA•MODERATEOdyne Hybrid System BatteryOdyne recalls hybrid systems (evAPU, G2V9) with Samsung SDI cells in Webasto battery packs due to fire risk.
FDA•MODERATEStraumann Bone Level Tapered ImplantStraumann recalls BLT Implant D 4.1mm RC SLActive 14mm due to possible 12mm length mismatch.
FDA•CRITICALBaxter Duo-Vent Solution SetBaxter recalls Duo-Vent Solution Set (1C8507) over air bubble risk in drip chamber and tubing.
FDA•CRITICALMorphine Sulfate Injection 2 mg/mL Prefilled SyringesFresenius Kabi recalls Morphine Sulfate 2 mg/mL syringes over a label mixup that may contain Dilaudid.
2 products