FDA•MODERATE
Da Vinci Surgical System E-Brake Retainer Pin
Intuitive Surgical is recalling the Da Vinci surgical system E-brake retainer pin due to a risk of uncontrolled motion and patient injury.
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FDA•MODERATETMJ Bilateral ImplantsTMJ Solutions is recalling custom temporomandibular joint implants due to incorrect components causing a poor fit and potential open bite.
NHTSA•MODERATEForest River Recreational TrailersForest River is recalling 2025-2027 NOBO, Ibex, and RPOD trailers due to mislabeled 110V circuits that pose an electrical shock risk.
NHTSA•MODERATEMaxxAir N-Series Maxxfan Rooftop Ventilation FansAirxcel is recalling MaxxAir N-Series Maxxfan rooftop ventilation fans due to a risk of fire from an overheating printed circuit board.
2 products
NHTSA•MODERATE2026 Indian Chief Vintage VIN LabelIndian Motorcycle is recalling 2026 Chief Vintage motorcycles due to an incorrect rear rim width listed on the VIN label.
FDA•MODERATEMorningstar Farms: 2 productsMorningStar Farms recalls Buffalo Chik'n Nuggets and Hot & Spicy Sausage Patties over possible plastic contamination.
2 products
CPSC•Arizer Solo III Portable VaporizersArizer is recalling Solo III portable vaporizers due to fire and burn hazards affecting specific serial prefixes and UPC 628078802274.
CPSC•BABESIDE Doll and Stroller Toy SetsBABESIDE doll and stroller sets are recalled due to a choking hazard from small parts that violate federal safety standards.
CPSC•GOPO Toys Pull String Teething ToysGOPO Toys is recalling pull string teething toys due to a serious choking hazard caused by strings that violate federal safety standards.
CPSC•Joolz Aer2 Car Seat AdaptersJoolz is recalling Aer2 car seat adapters because they can fail to attach to the stroller, posing a fall hazard to children.
CPSC•CooCooBaby Baby LoungersCooCooBaby is recalling Classic and Deluxe baby loungers due to suffocation and fall hazards that violate federal infant sleep safety standards.
CPSC•Michley Children's PajamasMichley children's pajamas are recalled for failing to meet federal flammability standards, posing a serious burn injury or death risk.
CPSC•Veseacky Children's Pajama SetsVeseacky children's pajama sets are recalled for violating federal safety standards, posing a serious burn injury or death risk to children.
FDA•MODERATEKeystone Industries: Multiple Topical Anesthetic GelsKeystone recalls 20% benzocaine gels (Pearson, Quala, DHP, etc.) over defective seals.
7 products- Device RecallFDA•MODERATEHeartMate 3 LVAS Backup Battery
Thoratec recalls HeartMate 3 LVAS kits (model 106524US) due to 11V backup battery failures.
6 products 
FDA•MODERATEInspire Respiratory Sensing LeadInspire is recalling its Respiratory Sensing Lead (Model 4340) due to incorrect Use By Dates that may lead to premature revision surgery.
3 products
FDA•MODERATESplashwire Hydrophilic Guide WireMerit Medical is recalling various Splashwire Hydrophilic Guide Wire models due to unsealed pouches that may compromise device sterility.
2 products
NHTSA•MODERATEPiaggio Liberty 50 and 150 MotorcyclesPiaggio is recalling 2026 Liberty 50 and 150 motorcycles due to an electrical fault that may cause the headlights to unexpectedly turn off.
NHTSA•MODERATEToyota BZ, Lexus RZ, and Subaru Solterra Electric VehiclesToyota is recalling 2026 Toyota BZ, Lexus RZ, and Subaru Solterra EVs due to an ECU fault that may cause a loss of drive power.
NHTSA•MODERATEFarber Specialty Emergency Vehicles Touch ScreenFarber Specialty is recalling 2025-2026 emergency vehicles because the touchscreen may fail, disabling emergency lights and equipment.
NHTSA•MODERATECadillac Vistiq Third-Row Power SeatbackGM is recalling 2026-2027 Cadillac Vistiq vehicles because the third-row power seatback may fail to reverse, posing an entrapment risk.
FDA•MODERATEBuprenorphine HCl InjectionPar Health is recalling Buprenorphine HCl Injection due to crystallization identified as Buprenorphine free base.
FDA•MODERATETriathlon Universal Baseplate Size 3/4Stryker recalls Triathlon Universal Baseplates due to size mislabeling in packaging.
2 products
FDA•MODERATEMedline Red Rubber Latex Urethral CathetersMedline recalls Red Rubber Latex Urethral Catheters (REF DYND13508–DYND13522, DYND13614/16) over surface, connector, and diameter defects.
34 products
FDA•MODERATEGiraffe OmniBed Canopy SoffitGE HealthCare recalls Giraffe OmniBed incubator/warmer over canopy soffit fastener risk that could injure patients.
3 products
FDA•MODERATEConMed AirSeal 5 mm Access PortConMed recalls AirSeal 5 mm Access Port (iASB5-150) over overpressure alert risk.
11 products- Device RecallFDA•MODERATESTAAR ICL Calculation Software
Staar Surgical is recalling Version 8.00 of its ICL Calculation Software due to a coding error affecting toric lens orientation diagrams.
2 products 
CPSC•Arrogantf Spa Drain CoversArrogantf spa drain covers are recalled due to entrapment and drowning hazards, as they violate federal safety standards.
FDA•MODERATENutrisystem Chocolate CheesecakeNutrisystem is recalling Chocolate Cheesecake 2 oz packages due to an undeclared soy allergen.
FDA•MODERATEGreat Value Hawaiian Roll 4pkGreat Value Hawaiian Roll 4pk recalled over oily substance on food-contact packaging; product never reached store shelves.
FDA•MODERATEdirectCHECK ACT-LR Whole Blood Quality ControlAccriva Diagnostics is recalling directCHECK ACT-LR whole blood quality control, level 2, due to incorrect performance range labeling.
NHTSA•MODERATEStoryteller GXV Hilt Alternator PulleyStoryteller is recalling 2024-2026 GXV Hilt vehicles due to an alternator pulley failure that may cause a loss of power brakes and steering.
FDA•MODERATEAripiprazole 30 mg TabletsAjanta Pharma is recalling Aripiprazole 30 mg tablets due to a mix-up with Voriconazole 50 mg tablets.
FDA•MODERATEMedtronic O-arm O2 Imaging SystemMedtronic is recalling the O-arm O2 Imaging System due to a firmware anomaly that may cause image artifacts during clinical use.
FDA•MODERATEHarmonyAIR A-Series Surgical Lighting SystemHarmonyAIR A-Series surgical lights recalled: intensity buttons may detach.
2 products
FDA•MODERATEHarmonyAIR A-Series Surgical Lighting SystemSteris is recalling HarmonyAIR A-Series Surgical Lighting Systems due to a risk of paint delamination on the light heads.
NHTSA•MODERATEForest River XLR Toy Hauler Recreational TrailersForest River is recalling 2023-2024 XLR Toy Hauler trailers due to an incorrect GVWR that may lead to vehicle overloading and crash risk.
NHTSA•MODERATEWabash 2027 Van Trailer Rear Impact GuardWabash is recalling 2027 van trailers due to improperly tightened rear impact guard bolts that may fail to meet federal safety standards.