FDA•MODERATE
Neptune Smart Docking Station
Stryker is recalling the Neptune Smart Docking Station (120V) due to missing safety testing and a potential electrical shock risk.
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FDA•MODERATECovidien EndoStitch Polysorb Single Use Loading UnitCovidien is recalling EndoStitch Polysorb loading units (170053, 170071) due to packaging holes that may compromise sterility.
NHTSA•MODERATEGrand Design Reflection Fifth Wheel Shock BoltsGrand Design is recalling 2025-2026 Reflection fifth wheel trailers over incorrectly tightened shock bolts that may detach while driving.
FDA•MODERATEMotor City Pizza Co. 5 Cheese BreadMotor City Pizza Co. 5 Cheese Bread recalled over potential Salmonella contamination.
FDA•LOWLidocaine HCl Injection 2%Eugia US LLC is recalling Lidocaine HCl Injection 2% because the label wrap covers the barcode, making it difficult to scan.
- Device RecallFDA•MODERATEB. Braun CESK Northside Anesthesia Tray
B. Braun recalls CESK Northside Anesthesia Tray due to cracked adhesive tubing.
8 products 
FDA•MODERATECovidien Mon-a-Therm Esophageal StethoscopeCovidien recalls Mon-a-Therm Esophageal Stethoscope 400TM (REF 90042) due to lack of FDA clearance.
3 products
FDA•MODERATEExacta Mix Vented Micro-Volume InletBaxter is recalling Exacta Mix Vented Micro-Volume Inlet (Model H938175) due to incorrect filters that may cause flow and clinical issues.
FDA•CRITICALBD Spinal Tray with Quincke NeedleBD recalls Spinal Tray with Quincke Needle over quality issues in bupivacaine component.
10 products
FDA•MODERATECovidien Shiley Tracheostomy TubeCovidien is recalling Shiley Tracheostomy Tubes due to incorrect display box labeling.
FDA•MODERATEIvenix Infusion System Large Volume PumpFresenius Kabi is recalling the Ivenix Infusion System LVP due to a risk of the cassette loading lever breaking during use.
NHTSA•MODERATEForest River Wildwood and Salem Travel TrailersForest River is recalling 2024-2025 Wildwood and Salem travel trailers due to a fire hazard from incorrectly wired fireplace outlets.
NHTSA•MODERATEMercedes-Benz GLE and GLS Rear Seat Belt BoltsMercedes-Benz is recalling various 2026 GLE and GLS models because rear seat belt bolts may be loose, increasing the risk of injury in a crash.
FDA•MODERATEMedtronic 1x4 Pocket Adaptor KitMedtronic recalls 1x4 Pocket Adaptor Kit (Model 64001) due to incorrect Use-By-Dates.
2 products
FDA•MODERATEMedline Eye Tray-LF Convenience KitMedline is recalling Eye Tray-LF kits containing mislabeled Cardinal Health syringes that may lead to incorrect insulin dosing.
FDA•CRITICALMedline Anesthesia Trays with Huons BupivacaineMedline recalls anesthesia trays with Huons bupivacaine over quality and efficacy issues.
10 products
FDA•MODERATEPhilips Azurion System HDDPhilips recalls Azurion systems over aging HDDs that may cause loss of imaging or movement.
3 products
NHTSA•MODERATEARBOC Transit Bus Wheelchair Restraint RetractorARBOC is recalling certain 2025-2026 transit buses because the wheelchair restraint retractors may not lock, increasing the risk of injury.
NHTSA•MODERATEIC Bus EVSB Drive Motor Mounting BracketInternational is recalling 2026-2027 IC Bus EVSB school buses because the drive motor may detach due to improperly tightened mounting bolts.
NHTSA•MODERATEForest River Bus Wheelchair Restraint RetractorForest River Bus is recalling various 2025-2027 bus models due to QRT-3 wheelchair retractors that may fail to lock, increasing injury risk.
NHTSA•MODERATESubaru Forester Power MoonroofSubaru is recalling 2026 Forester and Forester Hybrid vehicles because the power moonroof glass may detach, creating a road hazard.
NHTSA•CRITICALMack Anthem, Pioneer, Pinnacle, and Granite Wheel Lug NutsMack is recalling various 2026-2027 truck models because loose wheel lug nuts may cause a wheel to detach, increasing crash risk.
NHTSA•CRITICALVolvo VAH, VN, VHD, VNL, and VNR TrucksVolvo is recalling certain 2026-2027 VAH, VN, VHD, VNL, and VNR trucks because loose lug nuts may cause a wheel to detach while driving.
NHTSA•MODERATEChevrolet Express and GMC Savana Steering ColumnGM is recalling 2026 Chevrolet Express and GMC Savana vehicles due to a steering column defect that may cause inaccurate gear selection.
FDA•LOWPred Mild Ophthalmic SuspensionAbbVie is recalling 10 mL bottles of Pred Mild ophthalmic suspension due to failed stability specifications.
FDA•MODERATEHydroMARK Breast Biopsy Site MarkerDevicor Medical is recalling HydroMARK breast biopsy site markers due to incorrect inner package labeling.
NHTSA•MODERATETiffin Open Trail, Wayfarer, and Midas Recreational VehiclesTiffin is recalling 2026-2027 Open Trail, Wayfarer, and 2026 Midas RVs due to non-compliant cargo capacity labels that may increase crash risk.
NHTSA•MODERATEEmber Touring Edition Recreational Trailer Shock BoltsEmber is recalling 2026-2027 Touring Edition trailers due to improperly tightened shock bolts that may detach and create a road hazard.
NHTSA•MODERATELexus and Toyota Instrument Panel ClusterToyota is recalling various Lexus and Toyota models because the instrument panel may fail to display critical safety warnings.
NHTSA•CRITICALFord Bronco Sport and Maverick Front Control ArmFord is recalling 2021-2026 Bronco Sport and 2022-2026 Maverick vehicles due to a risk of control arm separation and loss of vehicle control.
NHTSA•MODERATEFord Expedition and Lincoln Navigator Seat Belt PretensionerFord is recalling 2018-2022 Expedition and Lincoln Navigator vehicles due to a seat belt pretensioner defect that may prevent proper restraint.
NHTSA•MODERATEFord Explorer, Ranger, and Bronco EngineFord is recalling 2025-2026 Explorer, Ranger, and Bronco vehicles due to an engine failure risk that may cause a loss of drive power.
FDA•CRITICALOmnipod 5 PodsInsulet recalls Omnipod 5 Pods over cannula damage causing insulin leaks and under-delivery, risking DKA.
3 products
FDA•CRITICALTNVitamins and Doctor's Pride Moringa CapsulesTotal Nutrition is recalling TNVitamins and Doctor's Pride Moringa capsules due to potential Salmonella contamination.
FDA•LOWNicotine Transdermal System Patch 14 mgAveva is recalling 14 mg Nicotine Transdermal System Patches due to elevated levels of oxidative-related impurities.
NHTSA•CRITICALTiffin Motorhomes Fuel TankTiffin is recalling certain 2025-2026 GT1, GH1, and GH2 motorhomes due to a fuel tank puncture that poses a fire risk.
NHTSA•MODERATEAlliance Paradigm Curt Touring Coil Suspension Shock BoltsAlliance is recalling 2025-2027 Paradigm trailers with Curt Touring Coil Suspensions due to a risk of detached shock bolts causing road hazards.
NHTSA•MODERATEForest River Recreational Trailer Shock BoltsForest River is recalling certain 2026 Riverstone, 2026 Cedar Creek, and 2024 R-Pod trailers due to incorrectly tightened shock bolts.
NHTSA•MODERATEFord Ranger and Bronco Tire Placard LabelsFord is recalling 2026 Ranger and Bronco vehicles due to incorrect tire and weight capacity information on safety labels.
FDA•CRITICALMogo Pure Moringa Oleifera CapsulesMogo Moringa is recalling Pure Moringa Oleifera Capsules due to potential Salmonella Typhimurium contamination.
FDA•MODERATEHalyard Purezero Ultraviolet Nitrile Exam GlovesHalyard is recalling Purezero Ultraviolet Nitrile Exam Gloves due to a failure to meet chemical permeation performance specifications.
FDA•CRITICALAbiomed Automated Impella ControllerAbiomed is recalling the Automated Impella Controller due to hardware issues that may cause motor control, startup, or power failures.
NHTSA•MODERATEBrinkley Model Z Trailer Shock BoltsBrinkley is recalling 2025-2026 Model Z trailers because incorrectly tightened shock bolts may detach and create a road hazard.
NHTSA•MODERATECoach and Equipment Phoenix and Metrolite Wheelchair RetractorCoach and Equipment is recalling Phoenix and Metrolite buses with QRT-360 wheelchair retractors that may fail to lock during transit.
FDA•MODERATEFentanyl Citrate Sterile CADD for InjectionIntegraDose is recalling Fentanyl Citrate Sterile CADD for Injection (NDC 71139-6030-1) due to the product being subpotent.
FDA•MODERATEPhilips Azurion Image Guided Therapy SystemsPhilips is recalling various Azurion systems due to potential mechanical wear in the Float Tabletop control module affecting table movement.
2 products
FDA•MODERATEPhilips Azurion X-ray Tube Cooling Unit Deaeration HosePhilips recalls Azurion systems: deaeration hose may leak oil, causing cooling failure and low-dose fluoroscopy lockout.
4 products
FDA•MODERATESilastic Foley CathetersC.R. Bard is recalling Silastic Brand Foley Catheters due to surface staining on the devices.
NHTSA•MODERATEHonda and Acura Passenger Seat Weight SensorHonda and Acura are recalling various vehicles due to a faulty passenger seat weight sensor that may cause unintended air bag deployment.
NHTSA•MODERATEBentley Continental GT and GTC Front Axle DriveshaftBentley is recalling 2026 Continental GT and GTC vehicles due to an incorrect front axle driveshaft that may cause a loss of steering control.