FDA•MODERATE
Prodisc C SK U.S. Cervical Disc Implant
Centinel Spine is recalling Prodisc C SK U.S. cervical disc implants due to a labeling mix-up involving 5mm and 6mm height specifications.
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FDA•Gold Lion and ilum Chocolate Male Enhancement ProductsGear Isle is recalling Gold Lion and ilum chocolate male enhancement products due to undeclared sildenafil and tadalafil.
FDA•Webcol Large Alcohol Prep PadsCardinal Health is recalling Webcol Large Alcohol Prep Pads due to potential microbial contamination.
CPSC•Frigidaire Gas RangesFrigidaire is recalling 23 gas range models (serials VF52200000–VF54399999) due to delayed oven ignition posing a burn hazard.
CPSC•Amazon Basics Camping Folding Pocket KnifeAmazon Basics Camping Folding Pocket Knife (model B0DM5BJK3H) recalled due to blade mechanism failure and laceration hazard.
CPSC•Tainoki Fine Furniture Office ChairsTainoki is recalling office chairs (models M7016O, M7004O, M7074O) with bases that can bend, creating a fall hazard.
CPSC•Goregent Infant WalkerGoregent infant walkers (Model 901) sold on Amazon violate safety standards and pose fall hazards.
CPSC•Aisstxoer Adult Bicycle HelmetsAisstxoer model GH018L adult helmets (size large, pink) fail mandatory safety standards and may not protect in a crash.
CPSC•Specialized Turbo Como SL Electric Bicycle ForkSpecialized is recalling Turbo Como SL e-bike forks (2021–2026) due to fatigue crack risk causing fall hazard.
CPSC•Wagner 900 Series Power SteamersWagner is recalling 900 Series power steamers (models 905e, 915e, 925e) due to burn hazard from hot hose and water expulsion.
CPSC•BUILT LUUM Light Up TumblersBUILT LUUM light up tumblers (16–18 oz) recalled due to breakage exposing button cell batteries; choking and ingestion hazard to children.
FDA•MODERATERiverence Smoked Trout DipRiverence is recalling Smoked Trout Dip due to an undeclared milk allergen.
FDA•MODERATETramadol Hydrochloride Tablets, USP 50 mgAmneal is recalling tramadol 50 mg tablets (NDC 60219-2348-5) due to elevated N-nitroso-desmethyl-tramadol impurity.
FDA•MODERATEClonidine Transdermal System 0.2 mg/dayTeva Pharmaceuticals is recalling Clonidine Transdermal System 0.2 mg/day due to the use of an unapproved raw material.
3 products
NHTSA•MODERATEIC Bus CESB and EVSB School Bus Body Panel JointInternational is recalling 2023–2027 IC Bus CESB and 2025–2027 EVSB school buses over insufficient epoxy on body panel joints that may separate in a crash.
NHTSA•MODERATETerex Digger Utility Truck Pole Guide ArmTerex is recalling 2019–2026 General 65, 80, 95, C4000, C5000, C6000 digger trucks; pole guide arm may fall due to cracked weld.
NHTSA•MODERATELippert 8K AxleLippert is recalling certain 8K axles with incorrect seals that can cause oil leakage, bearing failure, and wheel loss.
NHTSA•MODERATEChevrolet Silverado / GMC Sierra Roof Rail Air Bag InflatorGM is recalling 2018–2019 Silverado and Sierra Crew Cab trucks over roof rail air bag inflator end cap detachment or rupture risk.
NHTSA•MODERATEFord Lincoln Navigator, Nautilus, Aviator, Explorer Image Processing ModuleFord is recalling certain 2022–2025 Lincoln Navigator, Nautilus, Aviator, and Explorer vehicles over Image Processing Module resets causing loss of rearview camera and ADAS features.
FDA•CRITICALBoston Scientific Essentio, Proponent, Accolade, and Altrua 2 PacemakersBoston Scientific is updating software for Essentio, Proponent, Accolade, and Altrua 2 pacemakers to address dual-chamber device performance.
3 products
FDA•MODERATECytal Wound Matrix 2-LayerIntegra LifeSciences is recalling Cytal Wound Matrix 2-Layer 5x5 cm dressings due to out-of-specification endotoxin results.
5 products- Device RecallFDA•MODERATEPhilips AneurysmFlow Software
Philips is recalling AneurysmFlow software due to unreliable MAFA ratio data that may lead to incorrect clinical treatment decisions.
FDA•CRITICALB. Braun Streamline Hemodialysis Bloodline SetB. Braun is recalling Streamline hemodialysis bloodline sets due to the risk of air bubble accumulation in the arterial line.
6 products- Device RecallFDA•MODERATELeksell Vantage Arc System
Elekta is recalling the Leksell Vantage Arc System because faulty locking mechanisms may cause coordinate shifts during procedures.
FDA•MODERATEMedline Neuro SpongesMedline is recalling various neuro sponges due to higher-than-expected endotoxin levels.
38 products
FDA•CRITICALMedline Namic Angiographic Control Syringe KitsAmerican Contract Systems is recalling Medline Namic Angiographic Control Syringe kits due to a risk of syringe disconnection during use.
FDA•MODERATEDonJoy IceMan Classic3 Cold Therapy UnitDJO is recalling the IceMan Classic3 cold therapy unit (model 11-0494) due to a broken connector that may interrupt cold therapy.
4 products
FDA•CRITICALMagnesium Sulfate in Water for Injection IV BagAmneal is recalling Magnesium Sulfate IV bags (NDC 70121-1720-3) due to product mix-up with Tranexamic Acid.
NHTSA•MODERATELexus NX350, NX250, RX350, TX350 Rearview CameraToyota is recalling Lexus NX350, NX250, RX350, and TX350 vehicles over rearview camera display failure that reduces rear visibility.
NHTSA•MODERATELand Rover Defender Seat Belt Anchorage BracketLand Rover is recalling 2026 Defender vehicles with defective third-row seat belt anchorage welds that may fail to restrain occupants.
NHTSA•MODERATEKeystone Montana Fifth Wheel WiringKeystone is recalling 2026 Montana fifth wheel trailers due to improperly secured wiring that may be damaged by the bedroom slide-out, creating fire risk.
FDA•MODERATEDiversatek Healthcare Viper 3-Stage Fixed Wire Balloon DilatorDiversatek Healthcare is recalling Viper 3-Stage Fixed Wire Balloon Dilators due to incorrect inflation tag information.
4 products
FDA•MODERATEBromfenac Ophthalmic Solution 0.07%Alembic Pharmaceuticals is recalling Bromfenac Ophthalmic Solution 0.07% (NDC 62332-583-03) due to failed impurities and degradation specifications.
FDA•LOWRemedy Gel Hydrocortisone 1%Island Kinetics is recalling Remedy Gel hydrocortisone 1% due to subpotency.
3 products
FDA•MODERATEDimension Creatinine Flex Reagent CartridgeSiemens is recalling Dimension Creatinine Flex reagent cartridges (lots GA6307, BA7005) due to potential imprecision in patient creatinine results.
FDA•Mama Grande Gorditas and Doraditas de AzucarMama Grande is recalling Gorditas and Doraditas de Azucar due to undeclared wheat and soy allergens.
FDA•MODERATEOctreotide Acetate for Injectable SuspensionTeva is recalling Octreotide Acetate for Injectable Suspension due to a lack of assurance of sterility.
6 products
FDA•MODERATECurosurf (poractant alfa) 240 mg Intratracheal SuspensionChiesi USA is recalling Curosurf 240 mg intratracheal suspension vials (NDC 10122-510-03) due to lack of sterility assurance.
FDA•MODERATEXanax XR Alprazolam 3 mg TabletsViatris is recalling Xanax XR 3 mg tablets (NDC 58151-506-91) due to failed dissolution specifications.
FDA•MODERATEStraumann Custom Abutment TiStraumann is recalling custom abutments manufactured with incorrect raw material.
2 products
NHTSA•MODERATEFord Explorer and Lincoln Aviator Seat Belt AnchorsFord is recalling 2020–2026 Explorer and Lincoln Aviator vehicles over improperly secured second-row seat belt anchors.
NHTSA•MODERATEHyundai Palisade Power Rear SeatsHyundai is recalling 2026 Palisade and Palisade Hybrid power rear seats that may fail to detect and trap a person.
NHTSA•MODERATEFord Maverick Moonroof Glass PanelFord is recalling 2025–2026 Maverick vehicles over moonroof glass that may detach and become a road hazard.
NHTSA•MODERATEFord F-Series Super Duty High Pressure Fuel PumpFord is recalling F-Super Duty F250–F550, F600, and F750 vehicles over high pressure fuel pump failure risk due to biodiesel deposits.
NHTSA•MODERATETiffin Motorhomes GT1, GH1, GH2 Seating Capacity LabelTiffin is recalling 2025–2026 GT1, GH1, and 2026 GH2 motorhomes with incorrect seating capacity labels that may result in unbelted passengers.
NHTSA•MODERATEFord F-59 and F-53 Brake LightsFord is recalling 2025–2026 F-59 and F-53 chassis vehicles; brake lights may remain illuminated when not braking, increasing crash risk.
NHTSA•MODERATEForest River Entourage Motorhome CCC LabelForest River is recalling 2025–2026 Entourage motorhomes with incorrect CCC labels stating 7 belted seats instead of 8, risking overload and crashes.
FDA•MODERATEAlbuterol Sulfate Inhalation Solution 0.5%Nephron SC recalling Albuterol Sulfate Inhalation Solution (NDC 69374-330-05) due to illegible labeling.
FDA•CRITICALMedical Action Industries Pack Cath BHHMedical Action Industries is recalling Pack Cath BHH kits due to a syringe adapter defect that may cause connection failure during use.
FDA•MODERATELucerne 2% Cottage CheeseAlbertsons is recalling 24 oz Lucerne 2% Cottage Cheese due to potential contamination with metal spring fragments.