FDA•MODERATE
COAPTIUM Connect
TISSIUM recalls COAPTIUM Connect nerve repair device over unsubstantiated 36-month shelf life.
8 productsFilters
Category
Agency
Severity
Date
Distributed in
All Recalls
Back to home ←
FDA•MODERATEBlom-Singer Classic Indwelling Voice ProsthesisBlom-Singer Classic Voice Prosthesis recalled due to incorrect labeling of flange types.
2 products
FDA•MODERATEGEM Premier 7000 with iQM3Instrumentation Laboratory recalls GEM Premier 7000 with iQM3 due to lysing bag solution concentration issue.
2 products
FDA•MODERATEU2 Total Knee System Femoral Offset BushingU2 Total Knee System femoral offset bushing recalled due to incorrect engraved numbering that may cause misorientation.
2 products- Equipment RecallNHTSA•MODERATEMopar Seat Belt Assemblies
Chrysler recalls Mopar rear seat belt assemblies that may twist and fail to retract, raising injury risk.
NHTSA•MODERATEDodge Hornet and Alfa Romeo Tonale Seat BeltsChrysler recalls Dodge Hornet and Alfa Romeo Tonale rear seat belts that may twist and fail to retract.
NHTSA•MODERATEMack TerraPro Steering Gearbox FastenersMack is recalling certain 2025 TerraPro trucks over steering gearbox fasteners that may loosen.
NHTSA•MODERATEJayco Eagle Auto Leveling JacksJayco recalls 2027 Eagle, Eagle SLE, and Sundance fifth wheels over auto leveling jacks lowering in transit.
NHTSA•CRITICALIsuzu NPR HD Liftgate Deck PinsUS Truck Body recalls 2025 Isuzu NPR HD liftgates: deck pins may break, causing platform to fall.
NHTSA•MODERATEToyota Camry Hybrid Instrument ClusterToyota recalls 2025-2026 Camry Hybrids over instrument cluster failure that can disable safety warnings.
NHTSA•MODERATERivian R1S/R1T Front Turn SignalsRivian recalls 2025-2026 R1S/R1T vehicles over front turn signals that may fail.
NHTSA•MODERATEInternational Windshield Wiper AssemblyInternational recalls certain 2027 HV, HX, LT, MV, and RH trucks over wiper disconnect risk.
NHTSA•MODERATEEvenflo Revolve180 Litemax NXT Child SeatEvenflo recalls Revolve180 Litemax NXT child seats over recline indicator issue.
2 products
NHTSA•MODERATEMack Anthem and Pioneer Roof Marker LightsMack recalls 2027 Anthem and Pioneer trucks over roof marker lights that may fail, increasing crash risk.
2 products
NHTSA•MODERATEVolvo VNL/VNR Roof Marker LightsVolvo recalls 2027 VNL/VNR trucks: roof marker lights may fail, reducing visibility and crash risk.
2 products
NHTSA•MODERATEToyota bZ Woodland Tow ConverterToyota recalls 2026 bZ Woodland tow converter: short circuit can disable stability control and keep brake lights on.
2 products
NHTSA•MODERATEToyota Tacoma Shock Absorber ReservoirsToyota recalls certain 2024-2025 Tacoma models over shock absorber reservoirs that may detach, posing a crash risk.
FDA•CRITICALGlutathione 200 mg/mL InjectionVictory Medical Center Pharmacy recalls Glutathione 200 mg/mL vials over bacterial endotoxin contamination.
FDA•MODERATEMedline Hudson RCI Heated Breathing CircuitMedline recalls Hudson RCI heated breathing circuits for infants due to connector thermal damage risk.
5 products
FDA•MODERATEAtellica CH Urine Albumin AssaySiemens recalls Atellica CH Urine Albumin assay over falsely depressed UN_c and A1c_E results and QC failures.
2 products
FDA•MODERATEMicroScan LabPro UpdateBeckman Coulter is recalling MicroScan LabPro Update Panel Update Software Update, MicroScan LabPro Update Panel 11 (US), due to potential incorrect antibiotic resistance results that may lead to delayed or inappropriate treatment.
2 products
FDA•MODERATE5-PLASMA Bivalirudin AMR Verification KitAniara recalls 5-PLASMA Bivalirudin AMR Verification Kit (Model 5D-45905) due to stability issues causing degradation of bivalirudin.
3 products
FDA•MODERATEPhilips Allura Xper Interventional Fluoroscopic X-Ray SystemsPhilips recalls Allura Xper X-ray systems over unauthorized HDDs causing loss of imaging, movement, or data.
5 products
FDA•MODERATEHardyDisk Cefiderocol 30µg Susceptibility DisksHardy Diagnostics recalls HardyDisk Cefiderocol 30µg disks due to incorrect cartridges that may cause false susceptibility results.
FDA•MODERATEU2 Total Knee System PSA Box TrialUnited Orthopedic recalls U2 Total Knee PSA Box Trials (models 9323-5511 thru 9323-5526) due to screw defect.
4 products
NHTSA•MODERATETesla Model 3 and Model Y HeadlightsTesla recalls certain Model 3 and Model Y vehicles over low beams that may be too bright, raising crash risk.
FDA•MODERATEDicyclomine Hydrochloride Capsules 10mgAurobindo recalls Dicyclomine HCl 10mg capsules due to shortfill and empty capsules.
FDA•MODERATEGE Portrait Core Services Software V1.2.0GE recalls Portrait Core Services SW V1.2.0 over a security vulnerability.
2 products
FDA•MODERATEHondashi Seasoning PacketsPack'n Fresh recalls Hondashi seasoning packets due to undeclared fish allergen.
FDA•MODERATEFilmArray NGDS Warrior PanelBiofire Defense recalls FilmArray NGDS Warrior Panel due to strain mismatches affecting test accuracy.
FDA•MODERATEGE MAC VU360 ElectrocardiographGE recalls MAC VU360 ECG over software issue that may mix patient data.
FDA•MODERATEMerge PACS Medical Imaging WorkstationMerge PACS workstation recalled over risk of displaying thumbnails from a prior patient study.
2 products
FDA•LOWSyva Emit Tox Tricyclic Antidepressant Calibrator/ControlsSiemens recalls Syva Emit Tox Tricyclic Antidepressant Calibrator/Controls due to out-of-specification sodium azide concentration.
FDA•LOWSyva Emit Disopyramide AssaySiemens recalls Syva Emit Disopyramide Assay due to out-of-spec sodium azide concentration; risk of mild irritation.
NHTSA•MODERATEEscape E13 F1 Refrigerator VentilationEscape is recalling 2025-2026 E13 F1 trailers over carbon monoxide buildup risk from refrigerator ventilation.
NHTSA•MODERATEWabash Van Trailer ABS LightWabash recalls 2027 Van Trailers over unlabeled ABS malfunction light, posing crash risk.
FDA•MODERATEMaquet Flow Anesthesia Machine VaporizerMaquet recalls Flow anesthesia machines over risk of insufficient anesthesia.
FDA•MODERATEStryker AHTO Tube Set PackagingStryker recalls AHTO Tube Set Packaging (Cat. 0250070600) over handpiece leaking.
5 products
FDA•MODERATEDialysis Change Tray Clear SequenceMedical Action recalls Dialysis Change Tray Clear Sequence (Model 78791) due to improper seal in needle-free access device.
FDA•MODERATEOXOS MC2 Portable X-Ray SystemOXOS Medical recalls MC2 Portable X-Ray System due to overheating circuit board.
2 products
FDA•MODERATEVector Pedicle Screw System Anti-TorqueInnovasis recalls Vector Pedicle Screw System anti-torque instrument (LS-749) due to undersized tip that may prevent engagement during surgery.
NHTSA•MODERATELeprechaun/Freelander RV House Battery BreakerForest River recalls 2027 Leprechaun/Freelander RVs over missing battery breaker, fire risk.
NHTSA•MODERATEGrote HeadlampsDaimler Trucks recalls Grote Headlamps (A66-41940-000 to -003) over low beam illumination failure.
- Vehicle RecallNHTSA•MODERATERosenbauer Commander Touch Screen Display
Rosenbauer recalls certain Commander, M2-106, and HV507 emergency vehicles over Weldon UV800 displays that may fail, disabling emergency lights and equipment.
FDA•CRITICALOptiray 350 Ioversol InjectionLiebel-Flarsheim recalls Optiray 350 Ioversol Injection 500 mL vials due to particulate matter (plastic, steel, glass).
2 products
FDA•CRITICALHalyard Cardiac Cath Pack with Medline ManifoldAVID Medical recalls Halyard kits with Medline manifolds due to particulate risk.
3 products
FDA•MODERATEmunevo DRIVE Powered Wheelchair Control SystemMunevo recalls wheelchair control systems over software calibration issue causing steering drift and collision risk.
- Device RecallFDA•MODERATEWASPLab WebApp Software
Copan WASP recalls WASPLab WebApp software over a result-overwrite issue.
FDA•MODERATERadial Jaw 4 Biopsy ForcepsBoston Scientific recalls Radial Jaw 4 biopsy forceps due to sterile barrier breach risk.
4 products
FDA•MODERATEFORWARD Oral Airway KitIntegrated Medcraft recalls FORWARD Oral Airway Kits due to possible occluded airway tip.
2 products