FDA•MODERATE
Welch Allyn Spot Vision Screener VS100
Welch Allyn is recalling the Spot Vision Screener VS100 due to a screen flickering issue that may pose a seizure risk to susceptible users.
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FDA•MODERATESterile Radiology Procedure Kits Model DYNDH1491BMedline is recalling Sterile Radiology Procedure Kits Model DYNDH1491B due to potential sterile pouch packaging breach.
NHTSA•MODERATELexus LX600 TransmissionToyota is recalling 2025–2026 Lexus LX600 vehicles for transmission solenoid failure that can cause loss of drive power and fire risk.
FDA•CRITICALYoung Again Pet Food Core Health Dog FoodYoung Again Pet Food Core Health Dog Food recalled for presumptive Salmonella; 10 lb and 25 lb bags affected.
FDA•MODERATEWawa Reduced Fat Milk 2% 16 ozWawa is recalling 16 oz pints of Reduced Fat Milk 2% due to potential plastic contamination.
4 products
FDA•MODERATEMidodrine Hydrochloride Tablets, USP 5 mgMajor Pharmaceuticals is recalling Midodrine Hydrochloride Tablets 5 mg (NDC 0904-6818-06) due to inadequately sealed blister packaging.
FDA•MODERATESee Luer Cap Set MPC-130Molded Products is recalling See Luer Cap Set MPC-130 due to threaded sleeve detachment risk.
NHTSA•MODERATEFord Escape and Lincoln Corsair High Voltage BatteryFord is recalling 2022–2026 Escape and 2023–2026 Corsair plug-in hybrids over high voltage battery defect risking power loss and fire.
NHTSA•MODERATEPrevost X3-45 Passenger Seat AnchorsPrevost is recalling 2025–2026 X3-45 buses over improperly installed passenger seat anchors.
NHTSA•MODERATEWinnebago View and Navion Rear Roof CapWinnebago is recalling 2020–2023 View and Navion RVs; rear roof cap may detach during transit.
NHTSA•CRITICALFord Transit Brake PedalFord is recalling 2025 Transit vehicles; brake pedal may disconnect, causing loss of brake function.
NHTSA•MODERATEShyft Blue Arc BA4L-800 Steering GearboxShyft is recalling 2024–2025 Blue Arc BA4L-800 vehicles; loose steering gearbox fasteners may cause loss of steering control.
FDA•MODERATEMedline Airway Exam Kit Biopsy ValveMedline is recalling Airway Exam Kits containing Olympus biopsy valves due to a risk of rubber fragments detaching during use.
8 products
FDA•CRITICALAbiomed Automated Impella ControllerAbiomed is recalling Automated Impella Controllers due to a potential delay in the "Purge System Blocked" alarm.
2 products
FDA•MODERATEConvatec EsteemBody Drainable PouchConvaTec is recalling the EsteemBody Drainable Pouch due to a manufacturing issue that may cause the pouch to leak.
3 products
NHTSA•MODERATEThomas Built Buses Heater HoseThomas Built Buses Saf-T-Liner EFX and HDX (2023–2026) recalled for loose heater hose clamps that may leak hot coolant inside the cabin.
- NHTSA•MODERATEThomas Built Saf-T-Liner EFX/HDX Heater Hose
Thomas Built Saf-T-Liner EFX/HDX buses recalled for improperly tightened heater hose clamps that may leak hot coolant inside the cabin.
FDA•MODERATEKLG Kesar MukhwasGanesha Enterprises is recalling KLG Kesar Mukhwas (200 gm) for undeclared food colorings and unapproved dye.
FDA•CRITICALRosabella Moringa Dietary Supplement CapsulesAmbrosia Brands is recalling Rosabella Moringa dietary supplement capsules due to potential Salmonella contamination.
FDA•MODERATESemaglutide Compounding IngredientHarbin Jixianglong Biotech is recalling Semaglutide for compounding use due to CGMP deviations and lack of required validation testing.
2 products
FDA•MODERATEAmantadine HCl Capsules 100 mgAvKARE is recalling Amantadine HCl Capsules 100 mg (NDC 50268-069-15) nationwide due to failed dissolution specifications.
FDA•MODERATEMedtronic MiniMed Infusion PumpsMedtronic is recalling various MiniMed infusion pumps due to risks of insulin over- or under-delivery that can cause severe health complications.
14 products
FDA•CRITICALCentrosFLO Hemodialysis CathetersMerit Medical is recalling 25+ models of CentrosFLO Hemodialysis Catheters due to a sheath design defect that may cause serious injury.
5 products
FDA•MODERATEMedline ENFit G-Tube Connector KitsMedline is recalling G-Tube care and discharge kits due to connector defects that may cause leakage and fluid loss.
2 products
NHTSA•MODERATE2022 Chevrolet Tahoe/Suburban/GMC Yukon Transmission Control ValveGM is recalling 2022 Tahoe, Suburban, Yukon, and Escalade models with 10-speed transmission over rear wheel lock-up risk.
NHTSA•MODERATEHyperax Volt RV 4x Bike CarrierCouture Co is recalling Hyperax Volt RV 4x bike carriers; vibrations may cause anchoring plates to fail and carrier to detach.
FDA•MODERATEPurina Nature's Match Sow & Pig Complete FeedPurina is recalling 50 lb bags of Nature's Match Sow & Pig Complete Feed (UPC 804273051451) due to elevated Deoxynivalenol levels.
FDA•CRITICALQuest Cat Food Chicken Freeze Dried NuggetsSteve's Real Food recalling Quest Cat Food Chicken Freeze Dried Nuggets (10 oz) over inadequate thiamine levels.
2 products
FDA•CRITICALIQF BlueberriesOregon Potato Company is recalling IQF blueberries in 30 lb. cases and 1400 lb. totes due to potential Listeria monocytogenes contamination.
FDA•CRITICALErbe Flexible CryoprobeErbe is recalling Flexible Cryoprobes (REF 20402-401) due to a risk of the probes rupturing or bursting during use.
4 products
FDA•MODERATEOlympus Endoscope Suction ValvesOlympus is recalling MAJ-1443 and MAJ-1444 endoscope suction valves due to compatibility issues with specific automated reprocessors.
4 products
NHTSA•MODERATEInternational MV Brake System with Adaptive Cruise ControlInternational is recalling 2026–2027 MV vehicles; ECU software may prevent brakes from engaging with adaptive cruise control.
NHTSA•MODERATECadillac Lyriq Rearview CameraGM is recalling 2024 Cadillac Lyriq vehicles with rearview camera failure that may increase crash risk.
NHTSA•MODERATEChevrolet Silverado and GMC Sierra Transmission Control ValveGM recalls Silverado and Sierra trucks over transmission control valve failure that can lock rear wheels.
NHTSA•MODERATENissan Rogue EngineNissan is recalling 2023–2025 Rogue vehicles with 1.5L VC-Turbo engines over oil breakdown and bearing seizure risk.
NHTSA•MODERATENissan Rogue Electronic Throttle BodyNissan is recalling 2024–2025 Rogue VC-Turbo models over electronic throttle body gears that may break and cause loss of drive power.
FDA•MODERATEXZL Jelly SnacksXZL Jelly Snacks are recalled due to undeclared FD&C Yellow #5, Yellow #6, and Red #40 food dyes.
FDA•CRITICALJunebar Chocolate Cherry Snack BarJunebar Chocolate Cherry Snack Bar is recalled due to undeclared milk and soy allergens.
4 products
FDA•CRITICALWhite Vein Advanced Alkaloids Chewable TabletsShaman Botanicals is recalling White Vein Advanced Alkaloids Chewable Tablets because the active ingredient exceeds the labeled amount.
2 products
FDA•MODERATEBurlington Medical Wrap ApronsBurlington Medical is recalling Wrap Aprons due to potential attenuation degradation that may reduce the product's lifespan.
13 products
FDA•MODERATEEmbrace Shoulder Instrument Drill TowerWaldemar Link is recalling the Embrace Shoulder Instrument Drill Tower due to incorrect article numbers in the surgical technique documentation.
2 products
NHTSA•MODERATEWestern Star 49X and 47X Battery ConnectionDTNA is recalling 2020–2027 Western Star 49X and 2021–2027 47X vehicles over battery connection short-circuit fire risk.
NHTSA•MODERATETriumph Motorcycles Alternator WiringTriumph is recalling 2022–2024 Bonneville, Street Twin, Speed Twin 900, and Scrambler 900 motorcycles due to alternator wiring short-circuit and overheating risk.
NHTSA•MODERATEXcellent Roadbreaker A/T TiresGeneral Rubber is recalling Xcellent Roadbreaker A/T LT305/65R17 tires (TIN ending "4324") over cracking and liner separation risks.
FDA•MODERATEBD Alaris System with Guardrails Suite MXBD Alaris System labeling lacks required TLS version specification for secure Wi-Fi communication with Point-of-Care Units.
FDA•MODERATEWellsley Farms Farm-Raised Atlantic SalmonWellsley Farms Farm-Raised Atlantic Salmon (32 oz) recalled for Listeria monocytogenes contamination.
FDA•MODERATEVergani 1944 Milano Pandoro Classico Gluten FreeItalianway Import is recalling Vergani 1944 Milano Pandoro Classico Gluten Free due to potential Teflon fragment contamination.
FDA•MODERATEAdbry (tralokinumab-ldrm) Injection 300 mg/2mLLEO Pharma is recalling Adbry injection autoinjectors (NDC 50222-350-91, 50222-350-02) due to wool fiber contamination affecting sterility.
FDA•MODERATEOrtho Dev. Trimax Lantern Knee Drill PlateOrtho Dev. Trimax Pegged Drill Plates for the Lantern Knee System are recalled due to a manufacturing error causing excessive bone cuts.
2 products
FDA•MODERATEArtegraft Vascular GraftLeMaitre Vascular is recalling Artegraft Vascular Grafts due to a labeling mix-up that resulted in incorrect lot information on packaging.