FDA•MODERATE
Versius Surgeon Console
CMR Surgical is recalling the Versius Surgeon Console due to a cybersecurity risk involving the Secure Boot feature.
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All Recalls
Back to home ←- 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
FDA•MODERATE5008X Blood Tubing SetsFresenius recalls 5008X Blood Tubing Sets over potential online port errors.
2 products
FDA•MODERATEIntracept Access InstrumentsBoston Scientific is recalling Intracept Access Instruments due to a potential sterile barrier breach that could lead to severe infection.
FDA•MODERATEEnovis EMPOWR 3D Knee InsertEncore Medical is recalling the EMPOWR 3D Knee Insert (11L 14MM) due to a packaging discrepancy involving incorrect product sizes.
2 products
FDA•MODERATEMasimo Radius VSM NIBP Cuff and ECG SetMasimo recalls Radius VSM NIBP cuffs and ECG sets over false heart-rate alarms and cuff edge irritation.
2 products
NHTSA•CRITICALBMW Engine Starter RelayBMW is recalling certain 530e, 740Le, and 330e iPerformance vehicles due to an engine starter relay that may corrode and cause a fire.
NHTSA•MODERATEHusqvarna and GasGas Motorcycle Rear Brake CaliperKTM is recalling certain Husqvarna and GasGas motorcycles because the rear brake caliper may crack and break, reducing braking ability.
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•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.
CPSC•Metalux Optimized High Bay LED Light FixturesCooper Lighting is recalling Metalux Optimized High Bay LED light fixtures due to a fire hazard from potential overheating.
CPSC•CVS Health Medicated Hemorrhoidal WipesCVS Health Medicated Hemorrhoidal Wipes are recalled due to non-child-resistant packaging, posing a risk of poisoning to young children.
CPSC•Junpower CR2032 Lithium Coin BatteriesJunpower CR2032 lithium coin batteries are recalled for lacking child-resistant packaging, posing a severe ingestion and chemical burn hazard.
CPSC•Gigglescape Under the Sea Popping ToyGigglescape Under the Sea Popping Toys are recalled due to a choking hazard caused by a detachable plastic dome.
CPSC•Topyond Pool Drain Ports with CoversTopyond pool drain ports are recalled due to entrapment and drowning hazards, as they violate federal pool safety standards.
CPSC•Roman Candles 8 Shot FireworksWinco Fireworks is recalling Roman Candles 8 Shot fireworks (Model RCLR-W8012) due to explosion and burn hazards from tube malfunctions.
CPSC•Unity 7 Shot Aerial Cake FireworksWinco Fireworks is recalling Unity 7 Shot aerial fireworks (model MEF6096) due to tip-over, explosion, and burn hazards.
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.