NHTSA•MODERATE
Midwest Automotive Design Recreational Vehicles
Alliance RV is recalling various 2020–2026 Midwest Automotive Design recreational vehicles due to a fire risk from an undersized ground cable.
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NHTSA•MODERATEFord Focus and Fusion Transmission ClutchFord is recalling 2015-2018 Focus and 2013-2016 Fusion vehicles due to a transmission clutch fracture risk that may cause a fire.
NHTSA•MODERATEFord F-150 Shift LeverFord is recalling 2018 F-150 vehicles due to a shift lever defect that may cause unintended gear selection and unexpected vehicle movement.
NHTSA•MODERATEFord Escape Power Window SystemFord is recalling 2017 Escape vehicles due to a power window system malfunction that increases the risk of injury.
NHTSA•MODERATEFord F-150 Daytime Running LampsFord is recalling 2018-2020 F-150 vehicles because the daytime running lamps may fail to dim, increasing the risk of a crash.
NHTSA•MODERATEFord F-150 TransmissionFord is recalling 2014 F-150 vehicles due to a transmission defect that may cause an unexpected downshift and loss of vehicle control.
NHTSA•MODERATELincoln Nautilus Steering Wheel Detection SystemFord is recalling 2019 Lincoln Nautilus vehicles because the lane center assist system may fail to detect hands-off steering.
FDA•MODERATEBudesonide Inhalation SuspensionSun Pharmaceutical is recalling Budesonide Inhalation Suspension (1mg/2mL) due to the presence of foreign black or brown particles.
FDA•MODERATEBreckenridge Pharmaceutical: multiple capsulesBreckenridge recalls Duloxetine 30mg and 60mg capsules due to N-nitroso-duloxetine impurity above FDA limit.
2 products
FDA•MODERATENeoSpan SuperElastic Compression StapleIn2bones USA is recalling 10+ variants of NeoSpan compression staples due to missing MR Conditional safety labeling.
2 products
FDA•MODERATECareFusion 213: Multiple Subsidiary Of Beckton SolutionsBD recalls ChloraPrep & PurPrep applicators due to lack of sterility assurance, posing infection risk.
10 products
FDA•MODERATEMicromed SD LTM 64 PLUS EEG AmplifierMicromed is recalling SD LTM 64 PLUS EEG amplifiers due to a potential one-second temporal delay that may cause misinterpretation of results.
FDA•MODERATECGuard Prime Carotid Stent SystemInspireMD recalls CGuard Prime Carotid Stent System (model CND0830) due to deployment complications.
6 products
FDA•MODERATECORFLO Safety PEG KitAvanos recalls CORFLO Safety PEG Kit (model 30-4320) due to supplier-recalled lidocaine.
20 products
FDA•MODERATEMahurkar Elite PASS TraysMozarc Medical is recalling Mahurkar Elite PASS Trays because the Tegaderm CHG dressing is missing from the packaging.
2 products
FDA•MODERATEGE Allia IGS 3 Pulse Angiographic X-ray SystemGE recalls Allia IGS 3 Pulse X-ray systems over electrical shock risk to service personnel.
5 products
FDA•MODERATEBicarby DialysateFresenius Medical Care is recalling Bicarby Dialysate due to a luer-lock leak issue that poses a slip and fall hazard.
FDA•MODERATEPlum Solo Precision IV PumpICU Medical recalls Plum Solo IV Pump over soft limit alert failure.
3 products
FDA•MODERATETDC VELOCE 23G Two Dimensional CutterD.O.R.C. recalls TDC VELOCE 23G cutter over loose outer knife risk.
3 products
FDA•MODERATEEXCOR Pediatric VAD Blood Pump PU ValvesBerlin Heart is recalling EXCOR Pediatric VAD Blood Pump PU Valves due to an expiration date mismatch that could delay surgical procedures.
FDA•MODERATESporeTraq Mail-In Spore Testing ServiceSporeTraq Mail-In Spore Testing Service recalled due to incorrect incubation process; model 1023780.
4 products
FDA•MODERATESharpoint Microsurgical KnifeSurgical Specialties Corporation is recalling Sharpoint microsurgical knives mislabeled as 2.2mm when they are actually 3.0mm.
FDA•MODERATEGrace Medical Stapes ProsthesisGrace Medical is recalling the Titanium/Fluoroplastic Piston Stapes Prosthesis due to incorrect functional length listed on the labeling.
FDA•MODERATEDa Vinci 5 NIR Handheld CameraIntuitive Surgical is recalling the da Vinci 5 NIR handheld camera system due to a risk of unintentional illumination activation.
2 products
NHTSA•MODERATE2027 IC Bus CESB Wheelchair Restraint RetractorInternational is recalling 2027 IC Bus CESB school buses because wheelchair restraint retractors may fail to lock, increasing injury risk.
NHTSA•MODERATEHonda and Acura Rear SubframeHonda is recalling various Pilot, Ridgeline, Passport, and Acura MDX vehicles due to potential rear subframe corrosion and suspension failure.
NHTSA•MODERATEHonda Tire Repair Kit Sealant BottleHonda is recalling tire repair kit sealant bottles in certain hybrid and fuel cell vehicles due to a risk of the cap detaching under pressure.
FDA•MODERATENiacin Extended-release Tablets 1,000 mgLannett is recalling Niacin Extended-release Tablets 1,000 mg due to failed dissolution specifications.
FDA•MODERATEKirkland Signature Ultra Strength AntacidKirkland Signature antacid recalled due to metallic particles in tablets.
23 products
FDA•MODERATEXyvona (levorphanol tartrate) 2mg TabletsForte BioPharma recalls Xyvona (levorphanol tartrate) 2mg tablets due to FDA denial of proprietary name.
2 products
FDA•MODERATEDeRoyal Covaderm Plus Vascular Access DressingDeRoyal is recalling Covaderm Plus Vascular Access Dressing (Ref 46-406) due to a lack of sterility assurance.
FDA•MODERATEAligned Medical Fluids KitWindstone Medical Packaging is recalling Aligned Medical AMS16835 Fluids Kits due to a supplier recall of the included Lidocaine injection.
FDA•MODERATEGE MAC 5 A4 and A5 Resting ECG Analysis SystemsGE is recalling MAC 5 A4 and A5 ECG systems due to a software error that may incorrectly associate clinical data with the wrong patient.
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.
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•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•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.