FDA•MODERATE
Paragon 28 Phantom Intramedullary Nail System Guide Rod
Paragon 28 is recalling the Phantom Hindfoot TTC/TC Ball Tipped Guide Rod (item P31-955-1800-S) due to sterile packaging breaches.
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NHTSA•MODERATEAltec AT Series Turntable FastenersAltec is recalling 2024-2026 AT Series vehicles due to improperly heat-treated turntable fasteners that may fail and cause separation.
FDA•MODERATEFARADRIVE Steerable Sheath Clear IDEBoston Scientific recalls FARADRIVE Steerable Sheath Clear IDE over valve damage risk that may cause air embolism.
4 products
NHTSA•MODERATEForetravel Realm Presidential Motorcoach MaxxAir Fan PCBForetravel recalls 2027 Realm Presidential Motorcoaches over MaxxAir fan PCB overheating fire risk.
2 products
NHTSA•MODERATEEvenflo Reo by Revolve360 Child Seat HeadrestEvenflo recalls Reo by Revolve360 child seats over headrest shift risk in a crash.
NHTSA•MODERATEGreat Dane Champion Dry Van Trailer Rear Impact GuardGreat Dane recalls 2027 Champion dry van trailers missing rear impact guard extension channels, increasing crash injury risk.
NHTSA•MODERATETurtle Top Terra Ford Transit Wheelchair LiftTurtle Top recalls 2026 Terra Ford Transit buses: wheelchair lift contactor may fail, causing unintended movement and injury risk.
FDA•MODERATETosoh ST AIA-Pack TestosteroneTosoh is recalling ST AIA-Pack Testosterone test kits due to potential for inaccurate results that may impact clinical treatment decisions.
NHTSA•MODERATEAltec AP45A Truck Boom Stow Switch WireAltec is recalling 2013-2025 AP45A trucks due to a damaged boom stow switch wire that may overheat and cause a fire.
NHTSA•MODERATEIC Bus EVSB and CESB School Bus Body PanelsInternational is recalling 2025-2027 IC Bus EVSB and CESB school buses due to body panel joints that may separate during a crash.
NHTSA•MODERATELand Rover Discovery Sport Rearview CameraLand Rover is recalling 2021-2025 Discovery Sport vehicles due to a rearview camera defect that may reduce driver visibility.
NHTSA•MODERATEJeep Gladiator and Wrangler Steel WheelsChrysler is recalling 2026 Jeep Gladiator and Wrangler vehicles due to steel wheels that may crack or detach, increasing crash risk.
2 products- NHTSA•MODERATEIC Bus CECB Body Panel Joints
IC Bus CECB buses recalled: body panel joints may lack epoxy, risking separation in crashes.
FDA•MODERATEBD ChloraPrep Clear ApplicatorsCareFusion is recalling BD ChloraPrep Clear sterile solution applicators due to a potential lack of sterility from incomplete packaging seals.
FDA•MODERATEPhotera 400 Phototherapy DeviceDaavlin recalls Photera 400 phototherapy device due to incorrect UV sensor gain causing inaccurate output.
3 products
FDA•MODERATEMedline Total Knee Pack Mixing Bowls and SpatulasMedline recalls Total Knee Pack kits with Zimmer Biomet mixing bowls and spatulas over sterility risk.
2 products
FDA•MODERATEVasoview Hemopro 2 Endoscopic Vessel Harvesting SystemVasoview Hemopro 2 Endoscopic Vessel Harvesting System is recalled due to an out-of-specification sterilization dose.
FDA•MODERATEMedtronic DLP Pediatric Arterial CannulaMedtronic recalls DLP Pediatric Arterial Cannula (CFN 77010) over loose foreign material with trace blood.
2 products
FDA•MODERATEPapablic Replacement Brush HeadsPapablic is recalling replacement brush heads over a choking hazard from breakage.
2 products
NHTSA•MODERATEOrange EV Terminal Truck Frame RailsOrange EV is recalling certain e-TRIEVER, T-Series, and HUSK-e terminal trucks due to frame rails that may crack and separate.
- Vehicle RecallNHTSA•MODERATEE-One Emergency Vehicles
E-One is recalling 2025-2026 Commercial, Typhoon N, and Cyclone N emergency vehicles due to a risk of sudden loss of drive power.
NHTSA•MODERATENissan Armada, Infiniti QX56, and QX80 Certification LabelsNissan is recalling certain Armada, QX56, and QX80 vehicles with 22-inch wheels due to incorrect GAWR labels that may lead to overloading.
FDA•MODERATECleviprex Injectable EmulsionChiesi USA is recalling Cleviprex (clevidipine injectable emulsion) 50 mg/100 mL vials due to a lack of assurance of sterility.
FDA•MODERATEBell Pharmaceuticals: Multiple Carbamide Peroxide ProductsBell Pharmaceuticals recalls carbamide peroxide 6.5% earwax removers (CVS Health, Clinere, TopCare, etc.) for subpotency.
11 products
NHTSA•MODERATEWinnebago Navion and View Rooftop Ventilation FanWinnebago is recalling 2027 Navion and View RVs with MaxxAir N-Series rooftop fans due to an overheating circuit board fire risk.
2 products
NHTSA•MODERATEHyundai Kona Rear Center Seat Belt BuckleHyundai is recalling 2025 Kona Electric and 2026 Kona vehicles because the rear center seat belt buckle may fail to restrain occupants.
NHTSA•MODERATEFord Explorer Roof Rail CoversFord is recalling 2016-2019 Explorer vehicles because roof rail covers may detach, creating a road hazard.
NHTSA•MODERATEFord Aviator and Explorer Second-Row SeatsFord is recalling 2020-2027 Aviator and 2020-2026 Explorer vehicles because a faulty seat switch may cause second-row seats to move unexpectedly.
- Equipment RecallNHTSA•MODERATEFord F-150 Integrated Trailer Module Accessory Kits
Ford is recalling ITRM accessory kits for 2021-2026 F-150s due to a potential loss of trailer brakes and lighting.
NHTSA•MODERATEWabash Dry Freight Truck Liftgate Deck PinsWabash is recalling 2025-2026 Dry Freight trucks because broken liftgate deck pins may cause the platform to fall, posing an injury risk.
FDA•MODERATENystatin Cream USPPadagis is recalling 15 g tubes of Nystatin Cream USP due to subpotent drug results found during stability testing.
FDA•MODERATEOptima XR200amx Radiographic SystemGE HealthCare recalls Optima XR200/220/240amx systems after column replacement due to risk of arm drop and patient injury.
3 products
FDA•MODERATEFunctional Formularies: 2 productsNutricia recalls Liquid Hope and Nourish organic meal replacement formulas due to subpotent Vitamin A.
2 products
FDA•MODERATEBoston Scientific Rapid Refill Continuous Injection SystemBoston Scientific is recalling the Rapid Refill Continuous Injection System due to a risk of syringe disconnection during use.
FDA•MODERATEICU Medical Plum Duo Infusion PumpICU Medical recalls Plum Duo Infusion Pump v1.2.3 due to risk of delivering up to twice the programmed VTBI.
2 products
FDA•MODERATEOlympus Toomey Evacuator 30ccOlympus recalls Toomey Evacuator 30cc (Model 188) over sterilization failure risk.
4 products
NHTSA•MODERATENAPA Steering Inner Tie Rod EndsTenneco Automotive is recalling NAPA steering inner tie rod ends distributed nationwide due to a risk of steering loss.
NHTSA•MODERATEGrand Design Lineage MaxxAir Rooftop Ventilation FanGrand Design is recalling 2026-2027 Lineage RVs with MaxxAir N-Series rooftop fans due to an overheating circuit board that poses a fire risk.
2 products- Equipment RecallNHTSA•MODERATEZoox Automated Driving System Software
Zoox is recalling ADS software that may fail to detect heavy smoke, increasing the risk of a crash in low-visibility conditions.
FDA•MODERATEVersius Surgeon ConsoleCMR Surgical is recalling the Versius Surgeon Console due to a cybersecurity risk involving the Secure Boot feature.
- Device RecallFDA•MODERATETMINI Miniature Robotic System Tracking Arrays
Think Surgical is recalling TMINI Femur and Tibia Tracking Arrays because a loose knob may cause surgical misalignment.
FDA•MODERATEOmniTract Surgical Retractor SystemIntegra LifeSciences is recalling the OmniTract Surgical Retractor System due to insufficient drying time instructions in the user manual.
FDA•MODERATEGSP Neonatal GALT KitThe GSP Neonatal GALT Kit is recalled due to reduced on-board stability, which may cause test failures and delays in patient results.
FDA•MODERATEFletcher CT/MR Shielded Applicator SetElekta recalls Fletcher CT/MR applicator set due to risk of IU tube tip detachment.
3 products
NHTSA•MODERATEVolvo VHD, VNL, VNR, VN, and VAH Steering KnucklesVolvo is recalling 2026 VHD, VNL, VNR, VN, and VAH trucks due to a risk of steering control loss from loose steering arm fasteners.
FDA•MODERATEPemetrexed for Injection 100mg/VialSomerset Therapeutics recalls Pemetrexed for Injection 100mg/Vial due to cGMP deviations.
4 products
FDA•MODERATEKlowen Custom Orthodontic SolutionKlowen is recalling the Custom Orthodontic Solution, model CIAS-800033, due to a defect that may cause incorrect bracket placement.
FDA•MODERATEAtellica CH Enzymatic Hemoglobin A1c AssaySiemens is recalling the Atellica CH Enzymatic Hemoglobin A1c assay (Material No. 11097536) due to potential for inaccurate patient results.
FDA•MODERATEMedline Anesthesia Kit Peds 90-LFMedline recalls Anesthesia Kit Peds 90-LF due to included temperature probe distribution error.
3 products
FDA•MODERATEGasco Industrial: Multiple Isopropyl Alcohol ProductsGasco recalls Isopropyl Alcohol 70% in multiple sizes due to subpotency, which may reduce antiseptic effectiveness.
6 products