NHTSA•MODERATE
Volkswagen Tiguan Rearview Camera
Volkswagen is recalling 2024 Tiguan vehicles because a software error may cause the rearview camera to fail to display at startup.
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NHTSA•MODERATEWabash Platform TrailersWabash is recalling 2019-2027 Platform trailers because missing conspicuity tape may reduce visibility and increase crash risk.
2 products
FDA•MODERATEGas-X Simethicone 125 mg SoftGelsHaleon is recalling Gas-X Simethicone 125 mg SoftGels (120 count), UPC 3 00674 35041 9, due to incomplete inactive ingredient labeling.
FDA•MODERATEWellnov Supplements: 14 Vitaminally LLC Chandler AzesWellnov recalls liquid multivitamins and supplements over cGMP deviations risking bacterial contamination and C. botulinum.
14 products
FDA•MODERATELiraglutide InjectionLupin is recalling Liraglutide Injection (NDC 70748-346-02 and 70748-346-03) due to white thread-like particulate matter in the cartridge.
NHTSA•MODERATEHyundai Santa Cruz and Tucson Forward Collision SystemHyundai is recalling 2025-2026 Santa Cruz and Tucson vehicles because a software error may cause the brakes to apply unexpectedly.
NHTSA•MODERATETesla Model Y Certification LabelTesla is recalling 2025-2026 Model Y vehicles that may be missing a required certification label, posing a risk of vehicle overloading.
NHTSA•MODERATEHyundai Ioniq 5 and Ioniq 9 Rear Suspension FastenersHyundai is recalling 2025 Ioniq 5 and 2026 Ioniq 9 vehicles due to a risk of rear suspension fasteners loosening and causing loss of control.
NHTSA•MODERATEJerr-Dan XLP Carrier Light AssemblyJerr-Dan is recalling XLP Carrier kits due to non-compliant reverse and brake light assemblies that may increase the risk of a crash.
FDA•MODERATEICU Medical Oncology Extension SetICU Medical is recalling Oncology Extension Set REF: CL3960 due to a potential leak that could cause therapy interruption or hazardous exposure.
NHTSA•MODERATEKeystone Recreational Trailer Shock BoltsKeystone is recalling 2024-2026 Cougar, Alpine, Montana, and Walkabout trailers (NHTSA 26V313000) due to incorrectly tightened shock bolts.
NHTSA•MODERATEEndera Shuttle Transit Bus Wheelchair RetractorEndera is recalling 2025-2026 Shuttle transit buses because wheelchair restraint retractors may fail to lock, increasing injury risks.
NHTSA•MODERATEOshkosh NGDV Battery Electric VehicleOshkosh is recalling 2025 NGDV electric vehicles due to a battery contactor failure that may cause a sudden loss of drive power.
FDA•CRITICALPS Seasoning & Spices: 6 productsPS Seasoning recalls Ellsworth Sour Cream + Onion Seasoning and other seasonings over Salmonella risk.
6 products
FDA•MODERATETangent Single Use Digital CatheterTangent Endoscopy is recalling single-use digital catheters due to potential fractures at the distal shaft tip.
FDA•MODERATESwan-Ganz Catheters (Multiple Models)Becton, Dickinson and Company is recalling multiple variants of its Swan-Ganz pulmonary artery catheters due to a potential risk of valve leakage that may affect the balloon inflation performance.
3 products
NHTSA•MODERATEHyundai Elantra Hybrid Power Control UnitHyundai is recalling 2024-2026 Elantra Hybrid vehicles because the hybrid power control unit may overheat, increasing the risk of fire.
NHTSA•MODERATEHyundai Elantra and Elantra GT Air Bag InflatorHyundai is recalling 2015-2016 Elantra and 2016 Elantra GT vehicles because the driver's air bag inflator may rupture during deployment.
NHTSA•MODERATEAltec Aerial Device Emergency StopAltec is recalling various aerial device vehicles because the emergency stop may fail to halt hydraulic functions, increasing injury risk.
NHTSA•MODERATEHonda Prologue and Acura ZDX Rearview CameraHonda is recalling 2024-2025 Honda Prologue and 2024 Acura ZDX vehicles because the rearview camera may display a distorted or blank image.
NHTSA•MODERATEBMW C Evolution Motorcycle DC/DC ConverterBMW is recalling 2017-2018 C Evolution motorcycles due to a fire risk from potential corrosion in the DC/DC converter electrical connection.
NHTSA•MODERATECadillac, Chevrolet, and GMC Front Wheel Hub BoltsGM is recalling 2025–2026 Cadillac, Chevrolet, and GMC vehicles with 24-inch wheels due to incorrect front wheel hub bolts that may loosen.
FDA•CRITICALDOXOrubicin Hydrochloride Liposome InjectionSun Pharma recalls DOXOrubicin Liposome Injection 50 mg/25 mL vials due to glass particulate matter.
FDA•MODERATECodman CerebroFlo EVD CatheterIntegra LifeSciences is recalling the Codman CerebroFlo EVD Catheter due to out-of-specification endotoxin results.
FDA•CRITICALArrow Edge Hemodialysis Catheterization ProductArrow Edge hemodialysis catheterization product recalled: sheath introducer may not split, risking injury.
6 products
FDA•MODERATEBARD Dynamic Deca Steerable CatheterBARD Dynamic Deca Steerable EP catheter recalled due to incomplete seals on sterile product.
26 products
FDA•MODERATEEdwards EVOQUE Tricuspid Delivery SystemEdwards Lifesciences is updating the labeling for the EVOQUE tricuspid delivery system to include a warning about potential functionality issues.
NHTSA•MODERATEWeldon UV800 Display UnitHale Products is recalling Weldon UV800 display units (part numbers 610-00060-080-51, 610-00060-080-50, 610-00060-081, 610-00091) due to failure.
NHTSA•MODERATEWaltco MDV Series Liftgate Deck PinsHiab is recalling Waltco MDV series liftgates because broken deck pins may cause the platform to fall, posing an injury risk.
NHTSA•MODERATELucid Air Gen 4 InverterLucid is recalling 2024-2025 Air vehicles due to a Gen 4 inverter defect that may cause a loss of drive power and increase crash risk.
FDA•MODERATECreamy Sesame NoodlesFly By Jing recalls Creamy Sesame Noodles over possible undeclared peanut allergen.
FDA•MODERATEZYMUTEST HIA IgG ELISA KitZYMUTEST HIA IgG ELISA kit lot FD1265 distributed with outdated flyer containing incorrect positive control values.
FDA•MODERATEPhilips Azurion Cable Hose CarrierPhilips is recalling Azurion imaging systems due to potential loosening or breakage of Cable Hose Carrier bolts and plastic parts.
FDA•MODERATEQuickVue Dipstick Strep A TestQuidel is recalling QuickVue Dipstick Strep A Test (REF 20108) due to risk of false positive results.
FDA•MODERATEThermedx FluidSmart Urology Tube SetStryker is recalling the FluidSmart Urology Tube Set (REF LL0006) due to the distribution of nonconforming products.
FDA•MODERATESelenia Dimensions Mammography SystemsHologic recalls Selenia Dimensions mammography systems over loose or broken internal bolts.
2 products
NHTSA•MODERATEVespa Rearview Mirror Warning LabelPiaggio is recalling 2026 Vespa GTV 310, Primavera 150, and Primavera 50 motorcycles (Officina 8 color) with missing rearview mirror warning labels.
NHTSA•MODERATEFord Escape and Lincoln Corsair Integrated Park ModuleFord is recalling 2026 Escape and Lincoln Corsair vehicles because a faulty park module can cause the vehicle to roll away.
NHTSA•MODERATEFord Bronco Molded-In-Color Hardtop Roof PanelsFord is recalling 2021-2022 Bronco vehicles with Molded-In-Color hardtop roof panels that may detach while driving, creating a road hazard.
NHTSA•MODERATELand Rover Range Rover Seat Belt Warning SystemLand Rover is recalling 2026 Range Rover, Velar, and Sport vehicles (NHTSA 26V297000) because the seat belt chime may not activate.
NHTSA•MODERATENova Bus LFS Transit Bus Driver Door WindowNova Bus is recalling 2019-2023 LFS transit buses because the driver's door window may be missing a required DOT code mark.
FDA•MODERATEMetoprolol Succinate Extended-Release Tablets 25 mgAscend Laboratories is recalling 25 mg Metoprolol Succinate Extended-Release Tablets due to failed dissolution testing.
FDA•MODERATEDexcom G7 CGM iOS AppDexcom recalls G7 CGM iOS App (v2.9.0–2.11.2) over glucose alert delays that may cause missed hypo/hyperglycemic events.
4 products
FDA•MODERATEBuprenorphine Hydrochloride Injection 0.3mg/mLEndo USA recalls Buprenorphine Hydrochloride Injection 0.3mg/mL vials (NDC 42023-179-05) due to particulate matter contamination.
FDA•MODERATEDiowave 250W Laser SystemDiowave 250W Laser System recalled; software update needed to correct power output exceeding FDA-cleared 60W limit.
FDA•MODERATELUCAS Chest Compression SystemJolife AB is recalling LUCAS 2, 3, and 3.1 chest compression systems due to missing service documentation.
2 products
NHTSA•MODERATEPrime Time Crusader Waste Holding Tank VentForest River recalls 2026 Prime Time Crusader trailers; waste tank vent may release sewer gas into cabin.
NHTSA•MODERATEInternational HV Service Brake SystemInternational is recalling 2026–2027 HV vehicles for delayed service brake release that increases crash risk.
NHTSA•MODERATEBeck/Arnley Lower Control Arm and Ball Joint AssembliesTenneco is recalling Beck/Arnley lower control arm and ball joint assemblies for 2018-2025 Subaru vehicles due to a steering loss risk.
NHTSA•MODERATEBraun Chrysler Pacifica Wheelchair Restraint RetractorBraun is recalling 2023-2026 Chrysler Pacifica vehicles because the wheelchair restraint retractor may fail to lock, increasing injury risk.