FDA•MODERATE
Imactis CT-Navigation System
GE Medical Systems is recalling Imactis CT-Navigation System (Models E85101LA, E85101LP) due to potential needle trajectory/tip position discordance.
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NHTSA•MODERATEMercedes-Benz GLC Center Rear Seat BeltMercedes-Benz is recalling 2026 GLC models with center rear seat belts that may fail to properly restrain child seats.
NHTSA•MODERATEHyundai Palisade Seat Belt Status IndicatorHyundai is recalling 2026 Palisade and Palisade Hybrid (Limited/Calligraphy trims) over faulty third-row seat belt status indicator that may fail to alert unfastened occupants.
NHTSA•MODERATEAltec AC Series Crane and DT Series Digger Derrick Chassis Lighting HarnessAltec is recalling 2025 AC Series Crane and DT Series Digger Derrick vehicles due to missing chassis lighting harness that may disable body or trailer lights.
2 products
NHTSA•MODERATEGrand Design Lineage Motorhome Entry StepsGrand Design is recalling 2025–2026 Lineage motorhomes; entry steps may deploy while in transit, increasing crash risk.
2 products
NHTSA•MODERATERam ProMaster Emergency Exit WindowBraun is recalling 2023–2024 Ram ProMaster vehicles with incorrect emergency exit window glass that fails FMVSS 226 safety standards.
NHTSA•MODERATEKia Telluride Hybrid Second-Row Power SeatKia is recalling 2027 Telluride Hybrid second-row power seats that may fail to detect and stop for a person.
FDA•MODERATEDexamethasone Sodium Phosphate Injection, USP 100 mg/10 mLSomerset Therapeutics is recalling Dexamethasone Sodium Phosphate Injection (NDC 70069-025-10/01) due to out-of-specification impurities at expiry.
FDA•LOWDatascope Cardiosave Battery Charging StationDatascope is recalling the Cardiosave battery charging station due to a screw defect in the left bay that prevents proper charging.
FDA•MODERATELeksell Gamma Knife Radiosurgery SystemElekta is recalling Leksell Gamma Knife Perfexion, Icon, and Esprit systems due to potential adapter misalignment during radiation delivery.
FDA•MODERATEArtegraft Vascular GraftLeMaitre Vascular is recalling the Artegraft Vascular Graft due to a labeling mix-up on the outer packaging.
FDA•MODERATEConvatec EsteemBody Drainable PouchConvaTec recalls EsteemBody drainable pouches over possible leakage from a manufacturing issue.
3 products
FDA•MODERATEAptima HPV AssayHologic is recalling the Aptima HPV Assay due to the potential for the test to generate invalid or false negative results.
FDA•MODERATECub Pediatric Crib Model FL19HStryker is recalling Cub Pediatric Crib Model FL19H over missing access door warning labels.
NHTSA•MODERATEIC Bus CESB and EVSB School Bus Body Panel JointInternational is recalling 2023–2027 IC Bus CESB and 2025–2027 EVSB school buses over insufficient epoxy on body panel joints that may separate in a crash.
NHTSA•MODERATETerex Digger Utility Truck Pole Guide ArmTerex is recalling 2019–2026 General 65, 80, 95, C4000, C5000, C6000 digger trucks; pole guide arm may fall due to cracked weld.
2 products
NHTSA•MODERATELippert 8K AxleLippert is recalling certain 8K axles with incorrect seals that can cause oil leakage, bearing failure, and wheel loss.
NHTSA•MODERATEChevrolet Silverado / GMC Sierra Roof Rail Air Bag InflatorGM is recalling 2018–2019 Silverado and Sierra Crew Cab trucks over roof rail air bag inflator end cap detachment or rupture risk.
2 products
NHTSA•MODERATEFord Lincoln Navigator, Nautilus, Aviator, Explorer Image Processing ModuleFord is recalling certain 2022–2025 Lincoln Navigator, Nautilus, Aviator, and Explorer vehicles over Image Processing Module resets causing loss of rearview camera and ADAS features.
FDA•MODERATESTA Liatest D-Di Assay KitDiagnostica Stago is recalling the STA Liatest D-Di kit due to a positive bias in D-Dimer measurements that may cause inaccurate test results.
2 products
FDA•MODERATEIcosapent Ethyl CapsulesZydus Pharmaceuticals is recalling Icosapent Ethyl Capsules due to oxidation, which can cause capsule melting and discoloration.
FDA•CRITICALWebcol Alcohol Prep Pads (70% Isopropyl Alcohol)Cardinal Health is recalling Webcol Alcohol Prep Pads (200-count boxes) due to microbial contamination that may pose infection risk.
3 products
FDA•MODERATEWelch Allyn Spot Vision Screener VS100Welch Allyn is recalling the Spot Vision Screener VS100 (software v3.2.0.1) due to a screen flickering issue that may trigger seizures.
NHTSA•MODERATELexus NX350, NX250, RX350, TX350 Rearview CameraToyota is recalling Lexus NX350, NX250, RX350, and TX350 vehicles over rearview camera display failure that reduces rear visibility.
NHTSA•MODERATELand Rover Defender Seat Belt Anchorage BracketLand Rover is recalling 2026 Defender vehicles with defective third-row seat belt anchorage welds that may fail to restrain occupants.
NHTSA•MODERATEKeystone Montana Fifth Wheel WiringKeystone is recalling 2026 Montana fifth wheel trailers due to improperly secured wiring that may be damaged by the bedroom slide-out, creating fire risk.
2 products
NHTSA•MODERATEFord Explorer and Lincoln Aviator Seat Belt AnchorsFord is recalling 2020–2026 Explorer and Lincoln Aviator vehicles over improperly secured second-row seat belt anchors.
2 products
NHTSA•MODERATEHyundai Palisade Power Rear SeatsHyundai is recalling 2026 Palisade and Palisade Hybrid power rear seats that may fail to detect and trap a person.
NHTSA•MODERATEFord Maverick Moonroof Glass PanelFord is recalling 2025–2026 Maverick vehicles over moonroof glass that may detach and become a road hazard.
NHTSA•MODERATEFord F-Series Super Duty High Pressure Fuel PumpFord is recalling F-Super Duty F250–F550, F600, and F750 vehicles over high pressure fuel pump failure risk due to biodiesel deposits.
NHTSA•MODERATETiffin Motorhomes GT1, GH1, GH2 Seating Capacity LabelTiffin is recalling 2025–2026 GT1, GH1, and 2026 GH2 motorhomes with incorrect seating capacity labels that may result in unbelted passengers.
NHTSA•MODERATEFord F-59 and F-53 Brake LightsFord is recalling 2025–2026 F-59 and F-53 chassis vehicles; brake lights may remain illuminated when not braking, increasing crash risk.
NHTSA•MODERATEForest River Entourage Motorhome CCC LabelForest River is recalling 2025–2026 Entourage motorhomes with incorrect CCC labels stating 7 belted seats instead of 8, risking overload and crashes.
FDA•MODERATEChildren's Ibuprofen Oral Suspension 100 mg/5mLTaro Pharmaceuticals is recalling Children's Ibuprofen Oral Suspension 100 mg/5mL (120 mL) due to gel-like masses and black particles.
- Device RecallFDA•MODERATECentricity Universal Viewer Software
GE recalls Centricity Universal Viewer software over credential exposure risk.
4 products 
NHTSA•MODERATEOrange EV Terminal Truck Training SeatOrange EV is recalling T-Series, e-TRIEVER, and HUSK-e terminal trucks with foldaway training seats that may fail to restrain occupants in a crash.
2 products
NHTSA•MODERATEFerrari 12Cilindri WindowsFerrari is recalling 2025–2026 12Cilindri vehicles with dark-tinted windows that reduce driver visibility and fail safety standards.
FDA•MODERATEID NOW Influenza A & B 2 Test KitAbbott is recalling ID NOW Influenza A & B 2 test kits (Model 427-000) due to an increased rate of invalid results.
NHTSA•MODERATEMicro Bird G5 Transit Bus Wheelchair Tie-DownMicro Bird is recalling 2026 G5 transit buses with wheelchair tie-downs that may not lock due to installation error.
NHTSA•MODERATEAltec Service Body and Aerial Device VehiclesAltec is recalling 2023–2026 Service Body and Aerial Device vehicles with incorrect tire pressure labels that may cause blowout or crash.
NHTSA•MODERATEMicro Bird Transit Bus Wheelchair Tie-DownMicro Bird is recalling MB II, G5, and T-Series transit buses with wheelchair tie-downs that may not lock due to installation error.
NHTSA•MODERATENew Flyer Transit Bus Accelera ELFA 3 Control SystemNew Flyer is recalling XE35, XE40, XE60, XHE40, and XHE60 transit buses with Accelera ELFA 3 control systems over unintended acceleration/deceleration risk.
NHTSA•MODERATEMicro Bird School Bus Wheelchair Tie-DownMicro Bird is recalling MB II, G5, and T-Series school buses (2003–2026) with wheelchair tie-downs that may not lock due to installation error.
NHTSA•MODERATECummins PD7000 Electric Drive System Control ModuleCummins PD7000 Electric Drive (part BES CM0904 EV104B) recalled for SCM software error causing unintended vehicle movement.
NHTSA•MODERATENissan Kicks and Sentra Front Seat FrameNissan is recalling 2026 Kicks and Sentra vehicles with insufficiently welded front seat frames that may loosen during a crash.
2 products
FDA•CRITICALOmnipod 5 PodsInsulet is recalling Omnipod 5 Pods due to a cannula defect that can cause insulin under-delivery and severe health risks.
FDA•MODERATEMedline Cardiac Procedure KitsMedline is recalling cardiac procedure kits to clarify that the included chest drainage units are intended for adult patients only.
FDA•MODERATEMedline Medcrest Surgical GownsMedline is recalling Medcrest surgical gowns due to fabric delamination risks that may lead to infection or delays in patient care.
3 products
FDA•MODERATELutronic CLARITY II Laser SystemLutronic is recalling CLARITY II Laser System (Model 1110200210) due to sparking and burn hazard.
NHTSA•MODERATEHonda CMX300, CMX500, CL500 Handlebar Lock ScrewHonda is recalling 2023–2025 CMX300, CMX500, and CL500 motorcycles; handlebar lock screw may detach and interfere with steering.