NHTSA•MODERATE
Toyota Camry Hybrid Instrument Cluster
Toyota recalls 2025-2026 Camry Hybrids over instrument cluster failure that can disable safety warnings.
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NHTSA•MODERATERivian R1S/R1T Front Turn SignalsRivian recalls 2025-2026 R1S/R1T vehicles over front turn signals that may fail.
NHTSA•MODERATEInternational Windshield Wiper AssemblyInternational recalls certain 2027 HV, HX, LT, MV, and RH trucks over wiper disconnect risk.
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•MODERATEMedline Hudson RCI Heated Breathing CircuitMedline recalls Hudson RCI heated breathing circuits for infants due to connector thermal damage risk.
5 products
FDA•MODERATERed Blood Cells, Leukocytes ReducedRhode Island Blood Center recalls Red Blood Cells, Leukocytes Reduced units from a malaria-endemic-area donor.
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•MODERATEWangshin Doenjang Soybean PasteWangshin Doenjang soybean paste recalled over undeclared anchovy (fish) allergen.
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•MODERATEBig Way Hot Pot Miso PasteBig Way Hot Pot Miso Paste recalled for undeclared milk allergen.
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•MODERATEHondashi Seasoning PacketsPack'n Fresh recalls Hondashi seasoning packets due to undeclared fish allergen.
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•MODERATEIntramedullary Bone Saw Blade AssemblyBiomet recalls Intramedullary Bone Saw Blade Assembly (Model 475620) over sterile barrier damage risk.
5 products
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.
FDA•MODERATEPeter Rabbit Organics Banana & Strawberry PureeCheer Pack recalls Peter Rabbit Organics Banana & Strawberry puree pouches over possible plastic strip release.
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•MODERATEAmerican Regent: multiple injectionsAmerican Regent recalls Adequan injections due to particulate matter including glass.
2 products
FDA•MODERATEmunevo DRIVE Powered Wheelchair Control SystemMunevo recalls wheelchair control systems over software calibration issue causing steering drift and collision risk.
FDA•MODERATENerivio Infinity BatteryTheranica recalls Nerivio Infinity over battery thermal-runway risk during charging.
- 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.
- Device RecallFDA•MODERATEREMISOL Advance Data Manager
Beckman Coulter recalls REMISOL Advance Data Manager over software error that may misreport combo assay results.
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•MODERATEUkrop's Homestyle Foods: 2 productsUkrop's recalls Bread Pudding with Vanilla Sauce due to possible metal fragments.
2 products
FSIS•MODERATECurry Chicken SaladMary's Harvest alerts on Curry Chicken Salad due to possible Listeria; no illnesses reported.
FDA•MODERATEPower Over Fiber Base ModuleTerex Utilities recalls Power Over Fiber Base Module due to missing laser certification and improper labeling.