FDA•MODERATE
Gemcitabine Injection
Hikma is recalling Gemcitabine Injection due to improper temperature storage.
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All Recalls
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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 KitWindstone Medical recalls DSAEK Pack-RX kits due to contaminated alcohol prep pads.
4 products- Device RecallFDA•MODERATERayCare 2024A SP1 Oncology Information Systems
RaySearch recalls RayCare 2024A SP1 over beam set delivery note data loss risk.
2 products 
FDA•CRITICALHillrom VOLARA System P.CIRCUIT KITBaxter recalls Hillrom VOLARA P.CIRCUIT KIT (REF M08085) over nebulizer cup leakage that may cause oxygen drop and ineffective treatment.
4 products- Device RecallFDA•MODERATEMedela ENFit Enteral Extension Set
Medela is recalling ENFit Enteral Extension Sets due to incorrect connectors that may cause delivery delays or misconnections.
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 detector lift movement.
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 Dilatation BalloonBoston Scientific recalls CRE Pro Wireguided Dilatation Balloons over 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.
FDA•MODERATEPilling Wecksorb NeurospongesTeleflex is recalling Pilling Wecksorb Neurosponges and Neurosponge Strips due to potential out-of-specification levels of endotoxins.
2 products
FDA•MODERATEBaxter Adapter for Head PositioningBaxter is recalling the Adapter for Head Positioning due to a risk of the accessory becoming loose and moving during patient positioning.
FDA•CRITICALSpring & Mulberry Date-Sweetened ChocolateSpring & Mulberry is recalling Mango Chili and Pecan Date-Sweetened Chocolate bars due to potential Salmonella contamination.
11 products
NHTSA•MODERATEHonda Odyssey Rearview CameraHonda is recalling 2018-2020 Odyssey vehicles because water intrusion can cause the rearview camera to fail, increasing the risk of a crash.
NHTSA•MODERATEBMW and Mini Integrated Brake SystemBMW is recalling various 2023-2025 BMW, Mini, and Rolls-Royce vehicles due to an integrated brake system malfunction that increases crash risk.
NHTSA•MODERATEMopar HeadlightsChrysler is recalling Mopar headlights that may flicker or fail, reducing vehicle visibility and violating federal safety standards.
NHTSA•MODERATERam 1500 Headlight WiringChrysler is recalling 2026 Ram 1500 vehicles due to headlight wiring issues that may cause parking and daytime running lights to fail.
NHTSA•MODERATEHonda Pilot and Passport Rear Subframe BoltsHonda is recalling 2026 Pilot and Passport vehicles due to improperly tightened rear subframe bolts that may cause stability loss.
FDA•MODERATELevothyroxine Sodium Tablets 300 mcgAccord Healthcare is recalling 300 mcg Levothyroxine Sodium Tablets due to subpotency.
FDA•MODERATEprednisoLONE Acetate Ophthalmic Suspension 1%Lupin Pharmaceuticals is recalling three sizes of prednisoLONE Acetate Ophthalmic Suspension 1% due to the presence of a foreign substance.
FDA•MODERATERemel GC Agar BaseRemel is recalling GC Agar Base plates due to a risk of reduced or no recovery of Neisseria gonorrhoeae strains.
FDA•CRITICALHamilton Medical Ventilator Coaxial Breathing CircuitHamilton Medical is recalling ventilator coaxial breathing circuits due to a risk of valve membrane adhesion and inadequate ventilation.
NHTSA•MODERATEEntegra Accolade and Jayco Seneca MotorhomesJayco is recalling 2027 Entegra Accolade and Jayco Seneca motorhomes because missing dinette brackets may cause the seating to detach.
NHTSA•MODERATETeko Triumph, Turbo, and Trophy VehiclesTeko is recalling 2026 Triumph, Turbo, and Trophy vehicles because a missing alert system prevents them from making required pedestrian sounds.
NHTSA•MODERATEJATCO Automatic Transmission Control Valve AssemblyNissan is recalling JATCO automatic transmission control valve assemblies that may fail to correctly display the selected gear.
NHTSA•MODERATELincoln Nautilus Hybrid and Explorer HybridFord is recalling certain 2024-2027 Lincoln Nautilus Hybrid and 2025-2027 Explorer Hybrid vehicles due to a missing pedestrian warning sound.
NHTSA•MODERATEFord Mustang and Mustang GTD Windshield WipersFord is recalling 2024–2026 Mustang and 2025–2026 Mustang GTD vehicles because cold weather can cause windshield wiper and washer malfunctions.
NHTSA•MODERATEFord Mustang Mach-E Rear Differential Pinion ShaftFord is recalling 2021-2023 Mustang Mach-E vehicles due to a risk of rear differential pinion shaft fracture and potential loss of drive power.
NHTSA•MODERATENissan Rogue Instrument PanelNissan is recalling 2026 Rogue vehicles because the instrument panel may fail to display the gear selection, increasing the risk of a crash.
NHTSA•MODERATEJeep Grand Wagoneer Brake System Control ModuleChrysler is recalling 2026 Jeep Grand Wagoneer and Grand Wagoneer L vehicles due to a software error that may cause a loss of brake assist.
NHTSA•MODERATEJeep Grand Cherokee and Wagoneer Transmission IndicatorChrysler is recalling certain 2022-2024 Jeep Grand Cherokee and Wagoneer vehicles due to a software error affecting the gear selection indicator.
FDA•MODERATEImuldosa (ustekinumab-srlf) InjectionAccord BioPharma is recalling Imuldosa (ustekinumab-srlf) 130 mg/26 mL injection vials due to a lack of assurance of sterility.
FDA•MODERATELe Chef Bakery: 2 productsLe Chef Bakery recalls Mini Tiramisu and Mini Italian Pastry Assortment for undeclared Yellow #5.
2 products
FDA•MODERATEMedline Arterial Access TraysMedline recalls arterial access kits with Huons lidocaine ampules over quality issues.
19 products
FDA•MODERATEMedacta Shoulder System Short Monobloc Stem BroachesMedacta is recalling Short Monobloc Stem Broaches for the Shoulder System due to a risk of humerus fracture during surgery.
NHTSA•MODERATETiffin Recreational Vehicle MaxxAir Rooftop FansTiffin is recalling various 2026-2027 recreational vehicles equipped with MaxxAir N-Series rooftop fans due to an overheating fire risk.
NHTSA•MODERATEJayco Alante and Entegra Vision Recreational VehiclesJayco is recalling 2024 Alante and Entegra Vision RVs due to incorrect weight labels that may lead to vehicle overloading.
FDA•MODERATEMedline Convenience Kits with Swan-Ganz CathetersMedline recalls convenience kits with Swan-Ganz catheters over leak/breakage risk.
9 products
NHTSA•MODERATEDiamond Coach VIP Motorcoach Wheelchair RetractorDiamond Coach is recalling 2025-2026 VIP motorcoaches with QRT-360 wheelchair retractors that may fail to lock, increasing injury risk.
NHTSA•MODERATE2025 Nissan Sentra DriveshaftNissan is recalling 2025 Sentra vehicles due to a potential driveshaft installation issue that may cause power loss or vehicle rollaway.
NHTSA•MODERATEAltec Digger Derrick Pole RackAltec is recalling 2023-2025 Digger Derrick vehicles due to an incorrect pole rack capacity rating that may increase the risk of a crash.
NHTSA•MODERATEThomas Built Saf-T-Liner HDX2 Entrance DoorDaimler Trucks is recalling 2026-2027 Thomas Built Saf-T-Liner HDX2 buses because the entrance door may fail to open or close.
- NHTSA•MODERATEThomas Built SAF-T-LINER School Bus Entrance Door
Daimler is recalling 2026-2027 Thomas Built SAF-T-LINER HDX2 and EFX2 school buses because the entrance door may fail to open or close.
FDA•CRITICALHigh Valley Orchard Chocolate Covered RaisinsHigh Valley Orchard Chocolate Covered Raisins are recalled due to undeclared peanuts caused by a mis-packaging error.
FDA•MODERATEBakr Brown Butter Chocolate Chunk Cookie DoughBakr Brown Butter Chocolate Chunk Cookie Dough is recalled due to an undeclared soy allergen.
FDA•MODERATEPovi-One 10% Povidone-Iodine Oral AntisepticElevate Oral Care is recalling Povi-One 10% Povidone-Iodine Oral Antiseptic due to sub-potency.
FDA•MODERATEIntera 3000 Hepatic Artery Infusion PumpBoston Scientific recalls Intera 3000 pump over drug pathway leakage risk.
FDA•MODERATEMedline Convenience Kits with 10mL Polycarbonate SyringesMedline recalls convenience kits with 10mL syringes over unapproved design changes.
23 products