NHTSA•MODERATE
Vermeer BC1800XL Brush Chipper Trailer Hydraulic Jack
Vermeer is recalling 2002-2026 BC1800XL brush chipper trailers because the hydraulic jack may extend unexpectedly, increasing crash risk.
Filters
Category
Agency
Severity
Date
Distributed in
All Recalls
Back to home ←
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•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
CPSC•Gudook Bicycle HelmetsGudook-branded bicycle helmets are recalled for failing to meet federal safety standards, posing a serious risk of head injury.
CPSC•Crenlux Pool Drain CoversCrenlux pool drain covers are recalled due to entrapment and drowning hazards that violate federal safety standards.
CPSC•Little Grape Land Nursing PillowsLittle Grape Land nursing pillows are recalled due to a suffocation hazard and failure to meet federal safety standards.
CPSC•Broqixin Pool Drain CoversBroqixin pool drain covers (Model 11064W) are recalled for failing to meet federal entrapment protection standards, posing a drowning hazard.
CPSC•SUNS International Residential Elevator Interlock SwitchesSUNS International is recalling residential elevator interlock switches that can fail to lock, posing a fall and crushing hazard.
CPSC•Tiny Land Children's Play TentsTiny Land children's play tents are recalled due to fiberglass poles that can shed fibers, posing a risk of skin and eye irritation.
CPSC•Vornado Small Room Tower HeatersVornado is recalling SRTH small room tower heaters due to a fire hazard caused by fan blades detaching and the unit overheating.
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.