FDA•MODERATE
MOSAIQ Oncology Information System
Elekta is recalling the MOSAIQ Oncology Information System due to a software error that may prevent the loading of baseline shift plans.
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FDA•MODERATEBoston Scientific Orca Air/Water and Suction ValvesBoston Scientific is recalling Orca single-use air/water and suction valves due to reports of the suction button sticking during use.
- Device RecallFDA•MODERATEMerlin Patient Care System Programmer Software
Abbott Medical is recalling Merlin PCS software for the Model 3330 programmer due to a potential failure to terminate pacing tests.
FDA•MODERATEBoston Scientific Clik X AnchorBoston Scientific is recalling the Clik X Anchor due to a potential lack of sterility assurance.
FDA•MODERATEBoston Scientific CSK ElectrodesBoston Scientific recalls CSK reusable electrodes over performance concerns.
4 products
NHTSA•MODERATEGreat Dane Champion Dry Van TrailersGreat Dane is recalling 2026 Champion dry van trailers because broken deck pins may cause the liftgate platform to fall.
NHTSA•MODERATEInternational HV Service BrakeInternational is recalling 2026-2027 HV vehicles due to a delayed service brake release that may increase the risk of a crash.
NHTSA•MODERATEAltec AC Series Crane Personnel JibAltec is recalling 2024-2026 AC Series Crane personnel jibs (IJ26) due to missing welds that may cause the platform to fall.
FDA•MODERATEMinocycline Hydrochloride 115 mg TabletsAscend Laboratories is recalling Minocycline Hydrochloride 115 mg tablets due to failed dissolution specifications.
FDA•MODERATENeuro Nourish Dietary SupplementSensory Supplement is recalling Neuro Nourish dietary supplement due to premature lipid oxidation causing off odors and bitter taste.
3 products
FDA•MODERATEZep Alcohol Sanitizer SprayZep Inc. is recalling 55-gallon containers of Alcohol Sanitizer Spray due to potential microbial contamination.
FDA•MODERATEAdvance Aluminum Chloride Gel Hemostatic KitInter-Med is recalling Aluminum Chloride Gel kits due to an incorrect package insert that provides dangerous first aid instructions.
FDA•MODERATEDragonfly Thai Ginger PowderDragonfly Thai Ginger Powder is being recalled due to potential lead contamination.
FDA•MODERATEHintermann Series Talar ImplantDT MedTech is recalling the Hintermann Series Talar Implant due to a labeling error that may result in the wrong implant being used.
FDA•MODERATESiemens Dimension Tacrolimus Flex Reagent CartridgeSiemens is recalling Dimension Tacrolimus Flex reagent cartridges due to a potential positive bias in test results.
FDA•MODERATEPark St. Deli Macaroni & CheesePark St. Deli Macaroni & Cheese is recalled due to an undeclared soy lecithin allergen.
NHTSA•MODERATEDenago EV Nomad, Scout, and Rover VehiclesDenago EV is recalling various Nomad, Scout, and Rover models because they may fail to emit required pedestrian warning sounds.
FDA•MODERATEFarm Rich Pizza Cheese CrunchersFarm Rich Pizza Cheese Crunchers recalled over possible metal pieces.
FDA•MODERATEMedartis APTUS Cannulated Compression ScrewsMedartis is recalling APTUS cannulated compression screws due to a manufacturing defect where the cannulation is not centered.
FDA•MODERATEEXENT AnalyserThe Binding Site is recalling the EXENT Analyser due to a software error that may cause inaccurate M-protein detection or measurements.
NHTSA•MODERATEFord Expedition Center ConsoleFord is recalling 2018–2024 Expedition vehicles because peeling chrome on the center console can create sharp edges, increasing injury risk.
NHTSA•MODERATEFord Mustang, Lincoln Nautilus, and Navigator Instrument ClusterFord is recalling 2019 Mustang, Nautilus, and Navigator vehicles because the instrument cluster may go blank, failing to show safety data.
NHTSA•MODERATEFord Explorer Powertrain Control ModuleFord is recalling 2024 Explorer vehicles with 2.3L engines over a PCM reset issue that can cause a vehicle rollaway risk.
NHTSA•MODERATEFord Focus Canister Purge ValveFord is recalling 2012–2018 Focus vehicles due to a faulty canister purge valve that may cause the engine to stall while driving.
NHTSA•MODERATECummins Clean Fuel Technologies 75DGE CNG Fuel SystemsNatural Gas Fuel Systems is recalling 75DGE CNG Fuel Systems as the support bracket may fail in a crash, posing a fire risk from fuel leaks.
NHTSA•MODERATEVermeer BC1800XL Brush Chipper Trailer Hydraulic JackVermeer is recalling 2002-2026 BC1800XL brush chipper trailers because the hydraulic jack may extend unexpectedly, increasing crash risk.
NHTSA•MODERATEFord F-150 Instrument ClusterFord is recalling 2017 F-150 vehicles because the instrument cluster may fail to illuminate in cold temperatures, increasing crash risk.
NHTSA•MODERATEMidwest Automotive Design Recreational VehiclesAlliance RV is recalling various 2020–2026 Midwest Automotive Design recreational vehicles due to a fire risk from an undersized ground cable.
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•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