NHTSA•MODERATE
International Windshield Wiper Assembly
International recalls certain 2027 HV, HX, LT, MV, and RH trucks over wiper disconnect risk.
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NHTSA•MODERATEEvenflo Revolve180 Litemax NXT Child SeatEvenflo recalls Revolve180 Litemax NXT child seats over recline indicator issue.
2 products
NHTSA•MODERATEMack Anthem and Pioneer Roof Marker LightsMack recalls 2027 Anthem and Pioneer trucks over roof marker lights that may fail, increasing crash risk.
2 products
NHTSA•MODERATEVolvo VNL/VNR Roof Marker LightsVolvo recalls 2027 VNL/VNR trucks: roof marker lights may fail, reducing visibility and crash risk.
2 products
NHTSA•MODERATEToyota bZ Woodland Tow ConverterToyota recalls 2026 bZ Woodland tow converter: short circuit can disable stability control and keep brake lights on.
2 products
NHTSA•MODERATEToyota Tacoma Shock Absorber ReservoirsToyota recalls certain 2024-2025 Tacoma models over shock absorber reservoirs that may detach, posing a crash risk.
FDA•CRITICALGlutathione 200 mg/mL InjectionVictory Medical Center Pharmacy recalls Glutathione 200 mg/mL vials over bacterial endotoxin contamination.
FDA•MODERATEMedline Hudson RCI Heated Breathing CircuitMedline recalls Hudson RCI heated breathing circuits for infants due to connector thermal damage risk.
5 products
FDA•CRITICALSura Tanmen Hot and Sour Flavor Ramen Noodle KitSura Tanmen ramen noodle kits recalled over undeclared fish in the Soba sauce packet.
FDA•MODERATEAtellica CH Urine Albumin AssaySiemens recalls Atellica CH Urine Albumin assay over falsely depressed UN_c and A1c_E results and QC failures.
2 products
FDA•MODERATEMicroScan LabPro UpdateBeckman Coulter is recalling MicroScan LabPro Update Panel Update Software Update, MicroScan LabPro Update Panel 11 (US), due to potential incorrect antibiotic resistance results that may lead to delayed or inappropriate treatment.
2 products
FDA•MODERATE5-PLASMA Bivalirudin AMR Verification KitAniara recalls 5-PLASMA Bivalirudin AMR Verification Kit (Model 5D-45905) due to stability issues causing degradation of bivalirudin.
3 products
FDA•MODERATEPhilips Allura Xper Interventional Fluoroscopic X-Ray SystemsPhilips recalls Allura Xper X-ray systems over unauthorized HDDs causing loss of imaging, movement, or data.
5 products
FDA•MODERATEHardyDisk Cefiderocol 30µg Susceptibility DisksHardy Diagnostics recalls HardyDisk Cefiderocol 30µg disks due to incorrect cartridges that may cause false susceptibility results.
FDA•MODERATEU2 Total Knee System PSA Box TrialUnited Orthopedic recalls U2 Total Knee PSA Box Trials (models 9323-5511 thru 9323-5526) due to screw defect.
4 products
NHTSA•MODERATETesla Model 3 and Model Y HeadlightsTesla recalls certain Model 3 and Model Y vehicles over low beams that may be too bright, raising crash risk.
FDA•MODERATEDicyclomine Hydrochloride Capsules 10mgAurobindo recalls Dicyclomine HCl 10mg capsules due to shortfill and empty capsules.
FDA•MODERATEGE Portrait Core Services Software V1.2.0GE recalls Portrait Core Services SW V1.2.0 over a security vulnerability.
2 products
FDA•MODERATEFilmArray NGDS Warrior PanelBiofire Defense recalls FilmArray NGDS Warrior Panel due to strain mismatches affecting test accuracy.
FDA•MODERATEGE MAC VU360 ElectrocardiographGE recalls MAC VU360 ECG over software issue that may mix patient data.
FDA•MODERATEMerge PACS Medical Imaging WorkstationMerge PACS workstation recalled over risk of displaying thumbnails from a prior patient study.
2 products
NHTSA•MODERATEEscape E13 F1 Refrigerator VentilationEscape is recalling 2025-2026 E13 F1 trailers over carbon monoxide buildup risk from refrigerator ventilation.
NHTSA•MODERATEWabash Van Trailer ABS LightWabash recalls 2027 Van Trailers over unlabeled ABS malfunction light, posing crash risk.
FDA•MODERATEMaquet Flow Anesthesia Machine VaporizerMaquet recalls Flow anesthesia machines over risk of insufficient anesthesia.
FDA•MODERATEStryker AHTO Tube Set PackagingStryker recalls AHTO Tube Set Packaging (Cat. 0250070600) over handpiece leaking.
5 products
FDA•MODERATEDialysis Change Tray Clear SequenceMedical Action recalls Dialysis Change Tray Clear Sequence (Model 78791) due to improper seal in needle-free access device.
FDA•MODERATEOXOS MC2 Portable X-Ray SystemOXOS Medical recalls MC2 Portable X-Ray System due to overheating circuit board.
2 products
FDA•MODERATEVector Pedicle Screw System Anti-TorqueInnovasis recalls Vector Pedicle Screw System anti-torque instrument (LS-749) due to undersized tip that may prevent engagement during surgery.
NHTSA•MODERATELeprechaun/Freelander RV House Battery BreakerForest River recalls 2027 Leprechaun/Freelander RVs over missing battery breaker, fire risk.
NHTSA•MODERATEGrote HeadlampsDaimler Trucks recalls Grote Headlamps (A66-41940-000 to -003) over low beam illumination failure.
- Vehicle RecallNHTSA•MODERATERosenbauer Commander Touch Screen Display
Rosenbauer recalls certain Commander, M2-106, and HV507 emergency vehicles over Weldon UV800 displays that may fail, disabling emergency lights and equipment.
FDA•CRITICALOptiray 350 Ioversol InjectionLiebel-Flarsheim recalls Optiray 350 Ioversol Injection 500 mL vials due to particulate matter (plastic, steel, glass).
2 products
FDA•CRITICALHalyard Cardiac Cath Pack with Medline ManifoldAVID Medical recalls Halyard kits with Medline manifolds due to particulate risk.
3 products
FDA•MODERATEmunevo DRIVE Powered Wheelchair Control SystemMunevo recalls wheelchair control systems over software calibration issue causing steering drift and collision risk.
- Device RecallFDA•MODERATEWASPLab WebApp Software
Copan WASP recalls WASPLab WebApp software over a result-overwrite issue.
FDA•MODERATERadial Jaw 4 Biopsy ForcepsBoston Scientific recalls Radial Jaw 4 biopsy forceps due to sterile barrier breach risk.
4 products
FDA•MODERATEFORWARD Oral Airway KitIntegrated Medcraft recalls FORWARD Oral Airway Kits due to possible occluded airway tip.
2 products- Device RecallFDA•MODERATEQuantum 4Front 2 Wheelchair Controller
Quantum Rehab recalls the Quantum 4Front 2 wheelchair controller over a software issue that can cause unexpected park brake stops.
13 products 
FDA•MODERATETherabody Theragun G4 PRO ChargerTherabody recalls Theragun G4 PRO charger due to fire risk from overheating cradle.
NHTSA•MODERATERoyal Truck Solar PanelAlamo Group recalls 2022-2026 Royal Truck Class 2 Traffic Control trucks with Wanco sign boards over solar panel detachment risk.
FDA•MODERATEPower Over Fiber Base ModuleTerex Utilities recalls Power Over Fiber Base Module due to missing laser certification and improper labeling.
NHTSA•MODERATEAutocar ACTT Terminal Tractor ABS ECUAutocar recalls 2023-2027 ACTT terminal tractors over ABS ECU separation risk.
NHTSA•MODERATEGenesis G80 Ignition Coil Ground BoltHyundai recalls 2027 Genesis G80 over loose ignition coil ground bolt that may cause engine stall.
NHTSA•MODERATEBrinkley Model I Exterior LadderBrinkley RV recalls 2027 Model I trailers: exterior ladder may detach, posing injury risk.
NHTSA•MODERATEWanco Compact Light Tower Fuel TankWanco recalls Compact Light Towers (part WLTT) over fuel tank crack/leak fire risk.
NHTSA•MODERATERam 1500 Seat Belt Buckle AnchorChrysler recalls 2019-2026 Ram 1500s over improperly installed second-row seat belt buckle anchors, increasing crash injury risk.
NHTSA•CRITICALWinnebago Ekko Motorhome GeneratorWinnebago recalls 2024-2025 Ekko motorhomes: touchscreen may turn on generator, risking CO poisoning.
NHTSA•MODERATEHonda CMX500/CMX300/SCL500 Handlebar Lock ScrewHonda recalls CMX500, CMX300, and SCL500 motorcycles over a handlebar lock screw that may detach and impair steering.
NHTSA•MODERATEChevrolet Silverado EV and GMC Sierra EV Steel WheelsGM recalls 2026 Silverado EV and Sierra EV over steel wheels that may crack, risking loss of control.
NHTSA•MODERATEGM High Voltage Battery ModuleGM recalls 2026 Cadillac Escalade IQ/IQL, GMC Sierra EV, Silverado EV over high voltage battery module risk.