NHTSA•MODERATE
Cornell Pump Trailer Tongue
Cornell recalls 2025 pump trailers over cracked tongue risk.
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NHTSA•MODERATEPeterbilt and Kenworth Seat Ventilation HarnessPACCAR recalls certain 2027 Peterbilt and Kenworth trucks over a seat ventilation harness short circuit fire risk.
NHTSA•MODERATEAltec AN/AA/AM Series Automatic Brake SystemAltec recalls certain AN/AA/AM Series and Digger Derrick vehicles due to improperly calibrated automatic braking system, risking delayed braking.
NHTSA•MODERATERossmonster Motorcoach Maxxfan PCBRossmonster recalls 2026 Skye, Baja, Havn motorcoaches with MaxxAir Maxxfan rooftop fans due to PCB overheating fire risk.
2 products
NHTSA•MODERATEBritax B-Safe Child Seat Carrying HandleBritax recalls certain B-Safe child seats over a carrying handle screw that may loosen and detach, posing a fall injury risk.
NHTSA•MODERATELiftgate Deck PinsMarathon Industries is recalling certain 2025 Ford F-650 SD vehicles because the liftgate deck pins may break, causing the liftgate to unexpectedly fall and posing an injury hazard.
FDA•MODERATECarbamazepine Tablets 200mgGSMS recalls Carbamazepine 200mg tablets over black specks.
FDA•MODERATEAcamprosate Calcium 333 mg TabletsMylan recalls Acamprosate Calcium 333 mg tablets over dissolution failure.
FDA•MODERATEEsteem Body Soft Convex Urostomy PouchConvaTec recalls Esteem Body Soft Convex Urostomy Pouches due to cap leakage risk.
FDA•MODERATEVeritas Standard Glenoid Baseplaterestor3d recalls Veritas Standard Glenoid Baseplate over screw hole machining defect.
2 products- Vehicle RecallNHTSA•MODERATEE-One Fire Trucks Hydraulic Valve
E-One recalls certain fire trucks over hydraulic valve failure that can delay response.
- Equipment RecallNHTSA•MODERATEAvride Automated Driving System Software
Avride is recalling ADS software versions prior to RC-01-05 that may cause unexpected vehicle movement, increasing crash risk.
FDA•MODERATECarbamazepine Tablets 200mgTaro recalls Carbamazepine 200mg tablets over black specks.
2 products
FDA•MODERATEFDI Automated Field Steam SterilizerFDI recalls Automated Field Steam Sterilizer over possible ground continuity loss in the water recovery system connector.
FDA•MODERATESyva EMIT 2000 Quinidine AssaySiemens recalls Syva EMIT 2000 Quinidine Assay over precision issues that may cause elevated readings and risk of cardiac arrhythmias.
2 products- Device RecallFDA•MODERATEBeckman Coulter DxC 500i Analyzer Modules
Beckman Coulter recalls DxC 500i Analyzer Modules (software ≤1.5) over a Parameter Package import defect that can yield erroneous results.
2 products 
NHTSA•MODERATEHolley Replacement Carburetors and Throttle Body KitsHolley recalls replacement carburetors and throttle body kits over throttle control loss risk.
NHTSA•MODERATEHeil Front Loader CNG Ladder Kit BoltHeil recalls front loader garbage trucks with CNG tailgate ladder kits; incorrect bolt may damage CNG cylinders, risking fire.
2 products
NHTSA•MODERATEHeil CNG Tailgate Ladder Kit BoltHeil recalls CNG tailgate ladder kits; incorrect bolt may damage CNG cylinders, posing fire risk.
NHTSA•MODERATETerex Digger Derrick Pole Guide Arm WeldmentTerex digger derrick trucks recalled: weld crack may drop pole guide arm, posing injury risk.
FDA•MODERATEPEMRYDI RTU Pemetrexed InjectionShilpa Medicare recalls PEMRYDI RTU vials over green discoloration.
2 products
FDA•MODERATELibtayo (cemiplimab-rwlc) InjectionRegeneron recalls Libtayo (cemiplimab-rwlc) Injection 350 mg/7 mL over sterility concerns.
FDA•LOWParagon 28 Navicular Cage Foot ImplantParagon 28 recalls Navicular Cage foot implant (Model 6123S R) due to elevated oxygen levels.
2 products
FDA•MODERATEGentherm Thermal Regulating SystemGentherm recalls thermal regulating systems over CPU board overheating that may cause shutdown.
3 products
FDA•MODERATEKidneyVault Portable Renal Perfusion SystemParagonix recalls KidneyVault perfusion system over firmware defect causing blank screen.
FDA•MODERATESiemens Healthineers Immulite 2000 SYP Syphilis ScreenSiemens Healthineers recalls Immulite 2000 SYP Syphilis Screen due to negative bias risk.
2 products
FDA•MODERATEHalyard LAVH Pack Clearify Visualization SystemAVID Medical recalls Halyard LAVH Pack (USAR053-11) due to possible leakage of the Clearify Visualization System.
2 products
FDA•MODERATEGetinge SERVO-U/SERVO-N Y Sensor ModuleGetinge recalls SERVO-U/N Y sensor module over missing safety electrical testing.
2 products
FDA•MODERATEOverStitch Suture CinchBoston Scientific recalls OverStitch Suture Cinch over deployment and suture-cutting failures.
2 products
FDA•MODERATETD Navio Midi Speech Generating DeviceTobii Dynavox recalls TD Navio Midi speech device over battery tab damage risk.
2 products
FDA•MODERATEArrow-LOK ImplantArrowhead recalls Arrow-LOK Implants over missing gamma radiation audit, risking infection.
2 products- Device RecallFDA•MODERATEARVIS Surgical Navigation System Gen 2
Kico Knee recalls ARVIS Surgical Navigation System Gen 2 over tilted eyepiece image from sensor issue.
2 products 
FDA•MODERATEPhilips Cardiac Workstation 5000Philips recalls Cardiac Workstation 5000 over intermittent inaccurate heart-rate data.
2 products
FDA•MODERATEDentsply Sirona Capsule MixerDentsply Sirona Capsule Mixer recalled over electrical discharge risk when unplugged.
FDA•MODERATEIntersurgical One-Piece Guedel AirwayIntersurgical recalls One-Piece Guedel Airway, size 00, ISO 5.0, Blue, due to potential occlusion.
2 products- Device RecallFDA•MODERATEHamilton Microlab STAR PCT Software
Foundation Medicine recalls Hamilton Microlab STAR PCT v2.0.0 over spontaneous software closures.
FDA•MODERATEEndoFLIP 1 SystemCovidien recalls EndoFLIP 1 System due to 24-hour limit flagging products as expired.
2 products
NHTSA•MODERATEHorton Ambulance Touchscreen DisplayHalcore recalls 2025-2026 Horton ambulances over touchscreen failure that can disable emergency lights and equipment.
FDA•MODERATEShoolin Pharma Chem: multiple drugsShoolin Pharma Chem recalls Sildenafil and Tadalafil APIs due to CGMP deviations.
5 products
FDA•MODERATEClear Eyes Maximum Itchy Eye ReliefClear Eyes Maximum Itchy Eye Relief recalled over potential sterility issues.
FDA•MODERATEPresource KitsCardinal Health is recalling multiple Presource procedural kits due to possible endotoxin contamination.
13 products
FDA•MODERATEBD Intravascular Administration and Extension SetsBD recalls IV administration and extension sets due to possible sterilization failure.
2 products
NHTSA•MODERATEFord Explorer Engine Rod BearingFord recalls 2026 Explorer 2.3L engines over rod bearing seizure risk.
NHTSA•MODERATEChevrolet Silverado 2500 / GMC Sierra 2500 Tire Pressure LabelGM recalls 2024-2025 Silverado 2500 and Sierra 2500 with 20-inch accessory wheels over incorrect tire pressure label.
2 products
NHTSA•MODERATEJeep Grand Cherokee Windshield WipersChrysler recalls 2026 Jeep Grand Cherokee and Grand Cherokee L over wiper failure risk.
NHTSA•MODERATEDodge Durango Rear SpoilerChrysler recalls 2021-2023 Dodge Durango rear spoilers that may detach, posing a crash risk.
NHTSA•MODERATERange Rover Front Suspension KnucklesLand Rover recalls 2016-2017 Range Rovers over incorrect front suspension knuckles that may cause loss of control.
NHTSA•MODERATENissan Altima Front Passenger Air BagsNissan recalls 2025 Altima over front air bags that may not deploy due to incorrect mounting fasteners.
NHTSA•MODERATEChrysler Rearview CameraChrysler recalls certain 2026-2027 Jeep, Ram, Chrysler, and Dodge vehicles over rearview camera display failure.
FDA•MODERATEERBECRYO 2 Cryosurgical UnitErbe USA recalls ERBECRYO 2 Cryosurgical Unit (Model 10402-000) over risk of cryoprobe rupture from CO2 leak.