FDA•MODERATE
Medartis APTUS Cannulated Compression Screws
Medartis is recalling APTUS cannulated compression screws due to a manufacturing defect where the cannulation is not centered.
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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•MODERATENeoSpan SuperElastic Compression StapleIn2bones USA is recalling 10+ variants of NeoSpan compression staples due to missing MR Conditional safety labeling.
2 products
FDA•LOWWeikfield Custard Powder Kesar PistaWeikfield recalls Kesar Pista Custard Powder 300g over mislabeled ingredient (Pista vs. Pistachio).
FDA•CRITICALCareFusion 213: Multiple Chlorhexidine Gluconate SolutionsBD recalls ChloraPrep Clear and FREPP Clear applicators due to sterility seal breach risk.
4 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•LOWEpinephrine Injection 1mg/mLFresenius Kabi is recalling Epinephrine Injection 1mg/mL vials due to out-of-specification stability test results.
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
NHTSA•CRITICALYamaha XTZ690 Motorcycle Turn SignalYamaha is recalling 2025 XTZ690 motorcycles because the turn signals may fail to operate, increasing the risk of a crash.
FDA•CRITICALHaleon US: multiple softgelsHaleon recalls Gas-X Extra Strength softgels (120 & 72 ct) over possible coolant contamination.
2 products
FDA•CRITICALThe Coffee Connexion: 4 Poly Bag And PackedsCheese sauce mixes and related products recalled over potential Salmonella from dry milk powder.
4 products
FDA•MODERATESharpoint Microsurgical KnifeSurgical Specialties Corporation is recalling Sharpoint microsurgical knives mislabeled as 2.2mm when they are actually 3.0mm.
FDA•CRITICALKayserBett IDA Pediatric Care BedKayserBett is recalling the IDA pediatric care bed due to an entrapment risk if the hand control is not locked while the child is unattended.
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•CRITICALJeep Wrangler and Gladiator Power Steering Pump WiringChrysler is recalling 2021-2025 Jeep Wrangler and Gladiator vehicles due to a risk of fire from the power steering pump wiring.
NHTSA•CRITICALChrysler Pacifica PHEV Battery PackChrysler is recalling 2020-2022 Pacifica PHEV vehicles due to a battery pack fire risk that can occur even when the vehicle is parked.
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.