NHTSA•MODERATE
Husqvarna and GasGas Motorcycle Rear Brake Caliper
KTM is recalling certain Husqvarna and GasGas motorcycles because the rear brake caliper may crack and break, reducing braking ability.
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NHTSA•MODERATEPeterbilt 579 and Kenworth T680 Air Brake ValvePACCAR is recalling certain 2026-2027 Peterbilt 579 and 2027 Kenworth T680 tractors due to an incorrectly installed air brake valve.
NHTSA•MODERATEForest River Wildwood and Salem Travel TrailersForest River is recalling 2026-2027 Wildwood and Salem travel trailers due to an incorrect GVWR on the Federal Placard.
NHTSA•MODERATEToyota and Lexus Rear Axle CarrierToyota is recalling 2026 Lexus TX and Toyota Grand Highlander vehicles due to a risk of rear axle carrier breakage and loss of vehicle control.
- Vehicle RecallNHTSA•MODERATEUtilimaster Velocity Strobe Light
Shyft is recalling 2016, 2019, and 2021 Utilimaster Velocity vehicles due to a strobe light short circuit that poses a fire risk.
2 products 
NHTSA•MODERATEBMW Starter MotorBMW recalls certain 2023-2026 models over starter motor fire risk.
FDA•MODERATEMethohexital Sodium 100 mg/10 mLQuVa Pharma is recalling Methohexital Sodium 100 mg/10 mL vials due to failed impurities and degradation specifications.
FDA•MODERATEMedline Remedy Specialized Silicone CreamMedline Remedy Specialized Silicone Cream is recalled due to an out-of-specification result for formaldehyde in the raw material.
FDA•MODERATEMethohexital Sodium for Injection 500 mgAvet Pharmaceuticals is recalling Methohexital Sodium for Injection 500 mg vials due to failed impurities and degradation specifications.
FDA•MODERATEAquacel Ag Surgical SP DressingConvaTec is recalling Aquacel Ag Surgical SP dressings because they were manufactured with a thickness exceeding specifications.
FDA•MODERATEWise Onion RingsWise Foods is recalling 3.75 oz bags of Onion Rings due to undeclared colors and the presence of an unapproved color additive.
FDA•MODERATEOlympus Single Use Distal CoverOlympus is replacing the previous design of the MAJ-2315 Single Use Distal Cover used with the EVIS EXERA III Duodenovideoscope.
NHTSA•MODERATEBraun Chevrolet Traverse Fuel Fill LineBraun is recalling 2026 Chevrolet Traverse vehicles due to a missing braze connection in the fuel fill line that poses a fire risk.
NHTSA•MODERATEKenway Towing Light Kits and Submersible LightsHarbor Freight is recalling Kenway towing and submersible lights that may fail to illuminate, increasing the risk of a crash.
NHTSA•MODERATESubaru Crosstrek, Forester, and Ascent Certification LabelsSubaru is recalling various Crosstrek, Forester, and Ascent models due to incorrect weight rating labels that may lead to vehicle overloading.
NHTSA•MODERATEWabash Econex Refrigerated Body Side Door StepWabash is recalling 2021-2026 Econex Refrigerated Body vehicles because the side door stirrup steps may detach, posing injury and crash risks.
NHTSA•MODERATETesla Model Y and Model 3Tesla recalls certain 2026 Model Y and 2024 Model 3 vehicles lacking knee air bags and other safety features.
NHTSA•MODERATEQ'Straint Max Wheelchair RetractorPrime-Time is recalling Q'Straint Max wheelchair retractors in 2025-2026 Ford Med Transit vans that may fail to lock and secure wheelchairs.
NHTSA•MODERATEToyota Tundra Load Carrying Capacity LabelSoutheast Toyota is recalling one 2026 Tundra truck due to an incorrect load carrying capacity label that violates federal safety standards.
FDA•MODERATECinacalcet Hydrochloride Tablets 30 mgCipla recalls Cinacalcet HCl 30 mg tablets due to nitrosamine impurity above ADI.
3 products
FDA•MODERATEDextroamphetamine/Amphetamine Extended-Release CapsulesLannett is recalling 5 mg Dextroamphetamine/Amphetamine ER capsules due to a labeling mix-up where capsules contain immediate-release pellets.
FDA•MODERATEAsclemed: Multiple Lidocaine Hcl InjectionsAsclemed recalls Accucaine kits and Lidocaine HCl Injection USP, 1% (10 mg/mL), 5 mL ampules due to lack of sterility assurance.
2 products
FDA•MODERATEA.T.S. 4000 TS Tourniquet Dual HoseZimmer Surgical recalls A.T.S. 4000 TS Tourniquet Dual Hose (Model 60-1812-101-00) due to sterility breach risk.
2 products
FDA•MODERATEGORE TAG Thoracic Branch EndoprosthesisW.L. Gore & Associates is recalling its GORE TAG Thoracic Branch Endoprosthesis due to a device defect.
2 products
FDA•CRITICALReprocessed Electrophysiology and Ultrasound CathetersMedline is recalling reprocessed catheters due to residual particulate matter that may cause infection or embolism.
FDA•MODERATEBard Acute Drainage TraysBard recalls acute drainage trays due to lidocaine ampoules made under deficient practices.
20 products
FDA•CRITICALMedtronic Harmony Delivery Catheter SystemMedtronic is recalling the Harmony Delivery Catheter System due to a manufacturing defect that may cause the distal tip to detach during use.
FDA•MODERATESolar GI System Water PerfusionLaborie is recalling Solar GI System configurations due to moisture accumulation that may affect pressure measurement performance.
FDA•MODERATECovidien Shiley Disposable Decannulation PlugCovidien recalls Shiley Disposable Decannulation Plug over incorrect non-DEHP labeling; product contains 30-35% DEHP.
2 products
NHTSA•MODERATEJayco Heartland Cyclone Travel and Fifth Wheel TrailersJayco is recalling 2026 Heartland Cyclone trailers due to a missing inverter ground connection that poses fire and electrical shock risks.
NHTSA•MODERATEJayco Seismic Fifth Toy HaulersJayco is recalling 2026 Seismic fifth toy haulers due to a missing grounding connection that poses fire and electrical shock risks.
NHTSA•CRITICALKia Telluride Power Seat MotorKia is recalling 2020-2024 Telluride vehicles due to a risk of fire from overheating front power seat motors.
NHTSA•CRITICALHyundai Ioniq 5 High Voltage BatteryHyundai is recalling 2023-2024 Ioniq 5 vehicles due to a high voltage battery defect that may cause a fire while parked or driving.
NHTSA•CRITICALKia EV6 and EV9 High Voltage BatteryKia is recalling 2022-2024 EV6 and 2024 EV9 vehicles due to a high voltage battery defect that may cause a fire while parked or driving.
NHTSA•MODERATEAltec Service Body Inverter AC WiringAltec is recalling 2022-2026 Service Body vehicles due to a wiring defect that may cause a short circuit and increase the risk of fire.
NHTSA•MODERATENissan Leaf Rear Seat Belt RetractorsNissan is recalling 2026 Leaf vehicles because rear seat belt retractors may fail to properly secure child restraint systems.
NHTSA•CRITICALCrestline Ford CCL166 Type III Emergency VehicleCrestline is recalling 2026 Ford CCL166 Type III emergency vehicles due to a fuel line puncture risk that may cause a fire.
NHTSA•MODERATEWarn Wireless Remote KitsWarn is recalling wireless remote kits (part numbers 90287 and 90289) that may cause unexpected winch movement, posing an injury risk.
2 products
FDA•MODERATEGlucagon Emergency KitLupin recalls Glucagon Emergency Kits due to a stability test failure that may impair emergency use.
3 products
FDA•MODERATEGemcitabine InjectionHikma is recalling Gemcitabine Injection due to improper temperature storage.
FDA•MODERATEZeiss Intrabeam Spherical ApplicatorZeiss is recalling the 1.5 cm Intrabeam Spherical Applicator (REF 304534-6000-557) due to failure to meet manufacturing specifications.
FDA•MODERATESiemens ARTIS icono Ceiling SuspensionSiemens is recalling the ARTIS icono ceiling suspension (Model 11328100) because monitor attachment screws may loosen over time.
FDA•CRITICALDSAEK Pack-RX Surgical Convenience KitDSAEK Pack-RX kits recalled due to contaminated alcohol prep pads; stop use and contact firm.
4 products
FDA•MODERATERayCare 2024A SP1 Oncology Information SystemsRaySearch recalls RayCare 2024A SP1 oncology software due to potential data loss in beam set delivery notes.
2 products
FDA•CRITICALHillrom Volara System Patient Circuit KitBaxter recalls Hillrom Volara P.CIRCUIT KIT (REF M08085) due to nebulizer cup leakage causing oxygen drop and ineffective treatment.
4 products
FDA•MODERATEAccuray Cyberknife Xchange Robotic Collimator ChangerAccuray is recalling the Xchange Robotic Collimator Changer for the Cyberknife system due to a risk of the collimator falling from its housing.
FDA•MODERATEARTIS icono biplaneSiemens recalls ARTIS icono biplane over potential loss of movement after detector lift height adjustment.
3 products
FDA•MODERATEAccuray Cyberknife Xchange Robotic Collimator ChangerAccuray is recalling the Cyberknife Xchange Robotic Collimator Changer due to a risk of the component falling from its housing.
FDA•MODERATECRE Pro Wireguided DilatorBoston Scientific recalls CRE Pro Wireguided dilator due to potential sterile pouch breach.
12 products
FDA•MODERATEIntelliCuff Portable Cuff Pressure ControllerThe IntelliCuff pressure controller may fail to maintain cuff pressure due to a system leakage error, causing the motor to run continuously.