FDA•MODERATE
Stryker InZone Detachment System
Stryker is recalling the InZone Detachment System due to premature battery drain that may prevent coil detachment during medical procedures.
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NHTSA•MODERATEAirstream Recreational Vehicle Maxxfan Ventilation FanAirstream is recalling certain 2026 Classic trailers and 2025-2027 Interstate RVs due to a fire risk from overheating Maxxfan circuit boards.
2 products
NHTSA•MODERATEHyundai Tucson Instrument Panel DisplayHyundai is recalling 2025-2026 Tucson vehicles due to a software error that may cause the instrument panel display to fail.
NHTSA•MODERATEFord Bronco Fender FlareFord is recalling 2022-2026 Bronco vehicles because improperly secured fender flares may detach, creating a road hazard.
NHTSA•MODERATEFord and Lincoln Transmission Park PawlFord is recalling various 2018-2021 Ford and Lincoln vehicles due to a transmission park pawl issue that may cause a vehicle rollaway.
NHTSA•MODERATEHarbinger Stripped Chassis Steering Gear BoltsHarbinger is recalling 2025 Stripped Chassis vehicles due to steering gear bolts that may loosen or break, increasing the risk of a crash.
2 products
NHTSA•MODERATEElgin Pelican High Voltage BatteryElgin is recalling 2024-2026 Pelican vehicles with Samsung SDI high voltage battery packs due to a fire risk from potential battery failure.
FDA•MODERATEDuloxetine Delayed-Release CapsulesDirect Rx is recalling 30 mg Duloxetine Delayed-Release capsules due to N-nitroso-duloxetine impurity levels exceeding FDA limits.
FDA•MODERATEAcumed Hexalobe ScrewsAcumed is recalling various hexalobe screws used in wrist fixation systems due to a risk of the screws breaking during use.
2 products
FDA•MODERATEAmgen Corlanor and Sensipar TabletsAmgen recalls Corlanor and Sensipar tablets over foreign substance contamination.
5 products
FDA•MODERATEZimmer Off-Axis Reamer GuideZimmer recalls Off-Axis Reamer Guide (Model 110040240) due to breakage risk from catching during reaming.
5 products
FDA•MODERATEPFM Medical Multi-Snare SetPFM Medical is recalling Multi-Snare Set catheter devices due to a failure to meet biocompatibility requirements for in-vitro cytotoxicity.
FDA•MODERATEVentec VOCSN+Pro Respiratory SystemVentec is recalling the VOCSN+Pro respiratory system because a damaged battery may prevent the backup alarm from sounding during power loss.
NHTSA•MODERATEGM Express and Savana Steering Gear AssemblyGM is recalling 2025-2026 Express and Savana vehicles due to a steering gear assembly nut that may not be properly tightened.
2 products
NHTSA•MODERATERockford Fosgate Amplifier KitsRockford is recalling four amplifier kit models due to a 150-amp fuse defect that poses a fire risk.
NHTSA•MODERATERicon S-Series and K-Series Wheelchair LiftsRicon is recalling S-Series and K-Series wheelchair lifts because a faulty electrical contactor may cause the lift to move unexpectedly.
FDA•MODERATEMethylergonovine Maleate TabletsMajor Pharmaceuticals is recalling 0.2 mg Methylergonovine Maleate Tablets due to subpotency.
FDA•MODERATEFenofibrate Capsules, USP 200 mgAjanta Pharma is recalling Fenofibrate Capsules, USP 200 mg, due to manufacturing process deviations.
FDA•MODERATEPhilips Avalon Fetal Monitor FM20Philips recalls Avalon Fetal Monitor FM20 over speaker connector issue that may cause loss of speaker output.
2 products
FDA•MODERATEDa Vinci Surgical System E-Brake Retainer PinIntuitive Surgical is recalling the Da Vinci surgical system E-brake retainer pin due to a risk of uncontrolled motion and patient injury.
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•CRITICALImpella CP Set with SmartAssistAbiomed is recalling Impella CP Sets with SmartAssist due to a risk of low purge pressure that may interrupt mechanical circulatory support.
FDA•MODERATEBD Connecta Luer-Lok StopcockBD is recalling Connecta Luer-Lok stopcocks due to a potential connection failure at Port C when using plastic luer-lok syringes.
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•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.