FDA•MODERATE
Philips Achieva 1.5T MRE
Philips recalls Achieva 1.5T MRE over stiffness value errors from incorrect voxel size settings.
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FDA•MODERATEHiResolution Bionic Ear M Zn-Air Battery PakAdvanced Bionics is recalling M Zn-Air Battery Paks for sound processors due to a non-compliant battery door design.
2 products
NHTSA•MODERATEProliance High Voltage BatteryABS is recalling Proliance High Voltage Batteries (part 20000114-AB) due to contactor failure causing loss of drive power.
FDA•MODERATEAlcon Research: Multiple Lubricant Eye GelsAlcon recalls Systane and GenTeal eye gels over sterility concerns.
2 products
FDA•MODERATEOmega-3-Acid Ethyl Esters CapsulesMajor Pharmaceuticals is recalling Omega-3-Acid Ethyl Esters Capsules due to failed stability testing for capsule shell loss on drying.
FDA•MODERATEDisposable Mixing Bowls with SpatulaZimmer is recalling Disposable Mixing Bowls with Spatula due to compromised sterile barrier seals that may lead to infection.
FDA•MODERATEMilestone Vacuum Bag SU Large Specimen ContainerMilestone is recalling Vacuum Bag SU Large specimen containers (Model 68409SS) due to possible reagent leakage.
FDA•MODERATEHealthmark Mesh Style Tip ProtectorsHealthmark is recalling Mesh Style Tip Protectors (models CSW-03-2.0 and CSW-04-4.0) because they lack required FDA clearance.
FDA•MODERATEKiwi Omni Vacuum Delivery SystemClinical Innovations is recalling the Kiwi Omni Vacuum Delivery System (Model VAC-6000MT) due to a risk of device breakage during use.
FDA•MODERATEGenius Digital Diagnostics System Review Station DisplayHologic is recalling Genius Review Station displays (Model CMP-01669) due to unauthorized user modifications to validated monitor settings.
- Vehicle RecallNHTSA•MODERATEUtilimaster Aeromaster Certification Label
Shyft is recalling 2022 Utilimaster Aeromaster vehicles with incorrect GVWR on certification label, risking overloading and crashes.
NHTSA•MODERATEAudi Q5 and SQ5 Seat BeltsAudi is recalling 2025 Q5 and SQ5 vehicles with defective driver and front passenger seat belts that may fail to restrain occupants.
FDA•MODERATEB. Braun Sterile Water for Injection 3000 mLB. Braun recalls Sterile Water for Injection 3000 mL bags over sterility and leakage risk.
4 products
NHTSA•MODERATEMack Pioneer and Anthem Rear Brake ModulatorMack is recalling 2025–2027 Pioneer and 2026–2027 Anthem trucks over rear brake modulator short-circuit risk affecting ABS and stability control.
NHTSA•MODERATEVolvo VNR and VNL Rear Brake ModulatorVolvo is recalling 2025–2027 VNR and VNL trucks with rear brake modulators that may short circuit and disable ABS and stability control.
NHTSA•MODERATEJeep Wagoneer S and Dodge Charger Instrument Panel DisplayChrysler is recalling 2024–2025 Jeep Wagoneer S and Dodge Charger EVs for instrument panel display failure that may hide critical safety information.
NHTSA•MODERATELand Rover Defender Fuel TankLand Rover is recalling 2026 Defender vehicles with defective fuel tanks that may leak in a crash, posing a fire risk.
FDA•MODERATEFreshKote Lubricant EyedropsHarrow Eye LLC is recalling FreshKote Lubricant Eyedrops (0.33 fl oz) due to lack of assurance of sterility.
NHTSA•MODERATEACDelco GMW DOT 3 Brake and Clutch FluidGM recalls ACDelco GMW DOT 3 brake fluid (lot #01977 091222) containing sediment that may reduce brake performance.
NHTSA•MODERATEToyota RAV4 Front Seat BracketsToyota is recalling 2025 RAV4 vehicles with improperly welded front seat brackets that may fail to restrain occupants in a crash.
NHTSA•MODERATERPM Freeride Recreational Trailer CooktopTrails West is recalling 2027 RPM Freeride trailers due to inverted cooktop flame fire risk.
FDA•MODERATESkin Script Blemish Spot TreatmentSkin Script Blemish Spot Treatment recalled over failed stability specifications; UPC 6 10563 13873 9.
FDA•MODERATEWindstone Custom Convenience Kits Pre Op KitWindstone recalls Custom Convenience Kits Pre Op Kit (Part AMS14433) due to potential IV backflow and priming issues.
3 products
FDA•MODERATEMicro-X Rover Mobile X-ray SystemMicro-X is recalling the Rover Mobile X-ray System due to a generator malfunction that can render the device inoperable.
FDA•MODERATEOxoid Salmonella 9-O Agglutinating SeraRemel Europe is recalling Oxoid Salmonella 9-O Agglutinating Sera due to potential cross-reactivity and misidentification risks.
FDA•MODERATEFoundationOne CDx Sequencing Agent SEQ0067Foundation Medicine is recalling Sequencing Agent SEQ0067 component of FoundationOne CDx due to possible false-positive BARD1 variants.
FDA•MODERATELSL Infant Central Line Dressing Change KitLSL Healthcare recalls Infant Central Line Dressing Change Kit (Model 2925H) due to non-sterile alcohol prep pads.
6 products
FDA•MODERATEArrow Echogenic Introducer NeedleArrow recalls Echogenic Introducer Needle due to incorrectly manufactured liquid adhesive.
13 products
FDA•MODERATEAccess Total T4 CalibratorBeckman Coulter is recalling Access Total T4 Calibrator (Catalog No. 33805) due to negative bias causing falsely low results on DxI 600/800 instruments.
FDA•MODERATEFlamingo Funnel SmallSurgiSmoke recalls Flamingo Funnel Small over sterilization drape nonconformance.
3 products
FDA•MODERATEOlympus OER-ELITE Connecting TubesOlympus recalls OER-ELITE connecting tubes (MAJ-2110) due to premature lock lever failure.
12 products
NHTSA•MODERATEVolkswagen Taos Fuel Pressure SensorVolkswagen is recalling 2025–2026 Taos vehicles; fuel pressure sensor may dislodge in a crash, causing fuel leakage and fire risk.
NHTSA•MODERATETesla Cybertruck Wheel StudTesla is recalling 2024–2026 Cybertruck with 18-inch steel wheels over wheel stud separation risk.
FDA•MODERATEnanOss 3D Advanced Bone Graft SubstituteXTANT Medical is recalling nanOss 3D bone graft substitutes due to an incorrect five-year shelf life label.
FDA•MODERATEFurosemide Tablets, USP 80 mgLeading Pharma is recalling Furosemide Tablets 80 mg (NDC 69315-118-01) due to N-nitroso-Furosemide above recommended limits.
FDA•MODERATEAvitene Ultrafoam Microfibrillar Collagen HemostatDavol is recalling Avitene Ultrafoam Microfibrillar Collagen Hemostat (Catalog 1050030) due to potential inspect fragment contamination.
NHTSA•MODERATEHyundai Elantra and Tucson Air Bag SensorHyundai recalls 2025 Elantra N and 2026 Tucson models for misassembled air bag sensors that may delay deployment.
NHTSA•MODERATETern RC8 Digital Display ClusterHexagon Purus is recalling 2025–2026 Tern RC8 vehicles; digital display may show incorrect air brake pressure.
NHTSA•MODERATEThomas Built SAF-T-LINER HDX2 Driver Seat Belt AnchorThomas Built SAF-T-LINER HDX2 (2026–2027) driver seat belt anchor may be improperly installed, risking restraint failure in a crash.
NHTSA•MODERATEForest River East to West College Avenue and Entrada FenderForest River is recalling 2026–2027 East to West College Avenue and Entrada RVs due to fender-to-tire contact risk.
- NHTSA•MODERATEThomas Built SAF-T-LINER HDX2 Driver Seat Belt Anchor
Thomas Built SAF-T-LINER HDX2 (2026–2027) driver seat belt anchor may be improperly installed, risking inadequate crash restraint.
NHTSA•MODERATEMitsubishi Outlander Liftgate Gas SpringMitsubishi is recalling 2014–2022 Outlander vehicles; liftgate gas springs may rupture or fail, causing unexpected drop.
NHTSA•MODERATEQ'Straint QRT-3 Wheelchair Restraint RetractorQ'Straint QRT-3 wheelchair retractors may fail to lock, risking wheelchair movement during transit.
FDA•MODERATEGentuity HF-OCT Imaging SystemGentuity is correcting HF-OCT Imaging System software (versions 21.11–23.3.13) to prevent inaccurate longitudinal measurements during imaging.
NHTSA•MODERATEGoodyear Eagle F1 Supersport TireGoodyear is recalling Eagle F1 Supersport tires (305/30ZR21, 255/35ZR20) over tread separation risk.
2 products
NHTSA•MODERATEAltec Digger Derrick and Aerial Device Front End RadarAltec is recalling 2025–2026 Digger Derrick and Aerial Device vehicles with improperly installed front radar that may cause unexpected brake activation.
NHTSA•MODERATEBlue Bird All American Transit Bus Windshield Wiper Blade AssemblyBlue Bird is recalling 2026 All American transit buses with loose windshield wiper blade retention nuts that may cause wiper failure and reduced visibility.
NHTSA•MODERATELand Rover and Jaguar DC-DC ConverterJaguar Land Rover is recalling certain 2019–2024 Range Rover, Discovery, F-Pace, and E-Pace models due to DC-DC converter failure causing loss of drive power and lighting.
NHTSA•MODERATEBlue Bird All American School Bus Windshield Wiper Blade AssemblyBlue Bird is recalling 2026–2027 All American school buses with loose windshield wiper blade fasteners that may reduce visibility and increase crash risk.
FDA•MODERATEClaravis (isotretinoin capsule, USP) 10 mgTeva is recalling Claravis 10 mg capsules (NDC 0555-1054-56, 0555-1054-86) due to out-of-specification Tretinoin impurity levels.
3 products