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Goal Zero YETI 3000X Power Stations
Goal Zero recalls YETI 3000X power stations due to fire and burn hazard from overheating circuit board.
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CPSC•JINHEZO Mini Waterproof LED Tea LightsJINHEZO Mini LED Tea Lights recalled due to accessible button batteries posing ingestion hazard.
CPSC•Koorlian MattressesKoorlian mattresses (Twin XL, 10") recalled for violating flammability standard, posing fire risk.
CPSC•KTM Off-Road MotorcyclesKTM recalls 2021-2024 GASGAS and Husqvarna off-road motorcycles due to rear brake caliper failure risk.
CPSC•Airedale Ventilation FansModine recalls Airedale ventilation fans in heat pumps due to fire hazard from motor short circuit.
CPSC•Workbless Pressure WashersWorkbless recalls electric pressure washers over shock and electrocution hazards.
FDA•MODERATEAmerican Contract Systems Procedure KitsAmerican Contract Systems recalls 9 procedure kits due to potential endotoxin variability in included neurological sponges.
3 products
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•MODERATEPrince Bakery: 4 Enriched Bleached FloursPrince Bakery recalls Italian and French breads over undeclared sesame in the ingredient statement.
4 products
FDA•Glutathione 200 mg/mL Sterile Multidose VialsOptimal Balance Pharmacy recalls Glutathione 200 mg/mL vials over bacterial endotoxin contamination.
FDA•MODERATEGifford's Power Play Fudge Ice CreamGifford's recalls Power Play Fudge ice cream (1 qt) over possible rubber pieces.
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•MODERATEWhole BloodSuncoast Communities Blood Bank recalls whole blood due to incomplete donor eligibility screening.
2 products
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•MODERATEOutshine Fruit Bar: 6 productsDreyer's recalls Outshine Fruit Bars over possible glass pieces.
6 products
FDA•MODERATEProlon Everyday Apulian Almond & Cocoa SpreadProlon Apulian Almond & Cocoa Spread recalled for undeclared tree nuts (hazelnut, cashew, pistachio).
FDA•MODERATECarbamazepine Tablets 200mgTaro recalls Carbamazepine 200mg tablets over black specks.
2 products
FDA•MODERATERed Blood Cells, Leukocytes ReducedOneBlood recalls Red Blood Cells, Leukocytes Reduced from a misregistered donor.
FDA•MODERATEMedtronic MiniMed 640G Insulin PumpMedtronic recalls loaner MiniMed 640G pumps (MMT-1711/1712) over cleaning damage risk.
3 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•MODERATELago XSpectral Instruments recalls Lago X over a missing "X-Ray On" banner during readiness check.
2 products
FDA•MODERATEProtein Cereal Cocoa CrunchProtein Cereal Cocoa Crunch recalled over undeclared soy allergen.
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•MODERATEProspector Popcorn: 4 productsProspector Popcorn recalls gourmet popcorn varieties over inaccurate nutrient declarations.
4 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