NHTSA•MODERATE
Shyft Blue Arc BA4L-800 Steering Gearbox
Shyft is recalling 2024–2025 Blue Arc BA4L-800 vehicles; loose steering gearbox fasteners may cause loss of steering control.
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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
CPSC•CheerKid Baby Bath SeatsCheerKid baby bath seats (Model BH-222) recalled for tipping risk and drowning hazard.
CPSC•Watkins Highlife Collection Spa Hydromassage Rotary JetsWatkins is recalling Hydromassage rotary jets in Highlife Collection spas (2023–2025) due to entanglement and drowning hazards from suction force.
CPSC•Beloems Adult Portable Bed Rails Model BL-BR201Beloems bed rails (model BL-BR201) recalled for entrapment, asphyxiation, and fall hazards.
CPSC•Fortemotus Direct Adult Portable Bed RailsFortemotus Direct recalls model USFTMTJAS008 adult bed rails (30"×30") sold Aug–Oct 2025 over entrapment, asphyxiation, and fall hazards.
CPSC•SOOWERY 6-Drawer DresserSOOWERY 6-Drawer Dressers (47.2" × 11.8" × 33.3") sold on Amazon pose tip-over and entrapment hazards without wall anchoring.
CPSC•Cositas Colombianas Magnetic Board GamesCositas Colombianas magnetic board games recalled due to loose magnets posing serious ingestion hazard to children.
CPSC•LShome Photoelectric Smoke Detector Fire AlarmsLShome smoke detector alarms (Model XG-7D04-KZ9Z) may fail to sound during fire due to sensing threshold defect.
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.
FDA•MODERATEPuracol and Puracol Plus Collagen Wound DressingsMedline is recalling Puracol and Puracol Plus wound dressings due to elevated endotoxin levels that may cause severe inflammatory responses.
FDA•MODERATEEndoVive Safety PEG KitBoston Scientific is recalling EndoVive Safety PEG Kits due to potentially compromised sterile packaging on included ChloraPrep swabsticks.
NHTSA•MODERATEVee Tyre Taiga AT TireVee Tyre Taiga AT tires (LT235/85R16) may separate, causing tire failure and crash risk.
NHTSA•MODERATEVolvo Trucks VNL Parking Brake SystemVolvo Trucks is recalling 2024–2027 VNL (4) vehicles for inadequate parking brake force in weight bias mode, risking rollaway.