FDA•MODERATE
GE MAC 5 A4 and A5 Resting ECG Analysis Systems
GE is recalling MAC 5 A4 and A5 ECG systems due to a software error that may incorrectly associate clinical data with the wrong patient.
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FDA•MODERATEBD Pyxis MedStation 4000 Fingerprint ScannerBD Pyxis MedStation 4000 recalled: fingerprint scanner may overheat, causing burns.
8 products
FDA•MODERATEMedrad Avanta Injection System Tube SetsBayer is recalling Avanta Multi-Patient Administration Tube Sets due to a fit issue that may cause connection instability during use.
FDA•CRITICALPencan Spinal Needle TraysB. Braun recalls Pencan spinal needle trays over potential quality issues with bupivacaine component.
6 products
NHTSA•MODERATEJayco Recreational VehiclesJayco is recalling 2026 Entegra Qwest SE, Condor, Granite Ridge, and Melbourne RVs due to a false taillight warning light on the display.
NHTSA•MODERATEEntegra Qwest and Jayco Melbourne Prestige RVsJayco is recalling 2026 Entegra Qwest and Jayco Melbourne Prestige RVs due to a potential false taillight warning light on the display.
NHTSA•MODERATEAston Martin Valkyrie Brake Master CylinderAston Martin is recalling 2024 Valkyrie vehicles with track suspension due to a brake seal defect that increases the risk of fire.
FDA•CRITICALDried Herring FishPrime Food is recalling 7 oz. Dried Herring Fish due to potential Clostridium botulinum contamination from improper evisceration.
FDA•MODERATELidocaine HCl Injection USPSpectra Medical Devices is recalling Lidocaine HCl Injection USP single-dose ampules due to a lack of assurance of sterility.
- Food RecallFDA•MODERATEAlbertsons: multiple undeclared allergens
121 Albertsons products recalled for undeclared tree nuts, fish, or shellfish.
121 products 
FDA•LOWYunker Energy & Health Herbal SupplementSato Pharmaceutical is recalling Yunker Energy & Health Herbal Supplement due to a failure to meet label claims for Vitamin E content.
FDA•MODERATEAmlodipine and Olmesartan Medoxomil TabletsAscend Laboratories is recalling Amlodipine and Olmesartan Medoxomil Tablets, 5mg/40mg, due to failed dissolution specifications.
FDA•MODERATEArvis Hip & Knee 3.0 Instrument SetKico recalls Arvis Hip & Knee 3.0 Instrument Set over magnet face wear/corrosion.
2 products
FDA•MODERATEShimadzu X-Ray Systems High Voltage GeneratorShimadzu recalls X-ray systems over generator contactor weld risk; full model list on FDA page.
2 products
FDA•MODERATEDuloxetine DR Capsules 30 mgAsclemed USA is recalling Duloxetine DR Capsules 30 mg due to the presence of a nitrosamine impurity above acceptable intake limits.
NHTSA•MODERATEBraun Ram ProMaster Wheelchair Seat BeltBraun is recalling 2026 Ram ProMaster vehicles with Q'Straint wheelchair seat belts due to a risk of improper occupant restraint.
NHTSA•MODERATEKia Telluride Driver Seat Belt RetractorKia is recalling 2027 Telluride and Telluride Hybrid vehicles because the driver seat belt may fail to extend, increasing injury risk.
NHTSA•MODERATEChrysler Pacifica and Voyager Front Seat Harness ConnectorBraun is recalling 2023-2026 Chrysler Pacifica and Voyager vehicles due to a harness connector defect that may prevent air bag deployment.
NHTSA•MODERATENova Bus LFS and LFS Artic Transit BusesNova Bus is recalling LFS and LFS Artic transit buses (1997-2024) because the low brake air pressure warning light may fail to illuminate.
FDA•MODERATEPhaseOne Antimicrobial Solution SprayerOculus Technologies is recalling PhaseOne Antimicrobial Solution due to sprayer spring corrosion that may contaminate the product.
FDA•MODERATECASE v7.0 Cardiac Testing SystemGE Medical is recalling the CASE v7.0 Cardiac Testing System due to a risk of electrical sparking at the printer head.
FDA•MODERATEHiRes Ultra 3D CI HiFocus Mid Scala Cochlear ImplantAdvanced Bionics is recalling the HiRes Ultra 3D CI HiFocus Mid Scala cochlear implant due to an incorrect shelf-life expiration date.
2 products
FDA•MODERATENeptune Smart Docking StationStryker is recalling the Neptune Smart Docking Station (120V) due to missing safety testing and a potential electrical shock risk.
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•CRITICALD'Dioses Fruit Pops: multiple undeclared allergens32 D'Dioses Fruit Pops products recalled for undeclared tree nuts or milk.
32 products
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.