NHTSA•MODERATE
Ford Escape and Lincoln Corsair High Voltage Battery
Ford is recalling 2022–2026 Escape and 2023–2026 Corsair plug-in hybrids over high voltage battery defect risking power loss and fire.
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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•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 fragment detachment during use.
8 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•MODERATESemaglutide Compounding APIHarbin Jixianglong Biotech is recalling Semaglutide API due to failures in process and bacterial endotoxin method validation.
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 potential insulin over- or under-delivery risks.
14 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•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•MODERATEBurlington Medical Wrap ApronsBurlington Medical is recalling Wrap Aprons due to potential attenuation degradation that may reduce their protective lifespan.
13 products
FDA•MODERATEEmbrace Shoulder Instrument Drill TowerWaldemar Link is recalling the Embrace Shoulder Instrument Drill Tower (645-081/62) due to incorrect article numbers in the surgical manual.
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 Drill Plates for the Lantern Knee System are recalled due to a manufacturing error causing excessive bone cut depth.
2 products
FDA•MODERATEArtegraft Vascular GraftLeMaitre Vascular is recalling the Artegraft Vascular Graft due to a labeling mix-up on the outer packaging.
FDA•MODERATEPuracol and Puracol Plus Collagen Wound DressingsMedline is recalling Puracol collagen 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 the 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.
NHTSA•MODERATENova Bus LFS Transit Bus Seat Mounting RailsNova Bus is recalling 2013–2020 LFS transit buses; seat mounting rails may crack and cause seats to fall.
NHTSA•MODERATEVizzoni Dreamliner A/T TiresVizzoni Dreamliner A/T tires (LT265/75R16) recalled for sidewall separation risk.
FDA•MODERATEFrozen Cooked Medium ShrimpH & N Group is recalling 1 lb bags of frozen cooked medium shrimp due to potential Cesium-137 contamination.
FDA•MODERATEHortex Spring Vegetable MixHortex Spring vegetable mix is being recalled due to potential glass contamination.
FDA•MODERATECetrorelix Acetate for Injection Kit 0.25 mgMeitheal Pharmaceuticals recalls Cetrorelix Acetate injection kits (NDC 71288-558-90) due to missing or duplicated needles.
FDA•MODERATERefleXion X1 Radiotherapy System Model RXM1000RefleXion X1 Radiotherapy System Model RXM1000 recalled for software defect causing incorrect radiation dose delivery.
FDA•MODERATEID NOW Influenza A & B 2 Test KitAbbott is recalling ID NOW Influenza A & B 2 test kits due to a higher-than-expected rate of invalid test results.
NHTSA•MODERATEHarley-Davidson Sportster S Upper Triple ClampHarley-Davidson is recalling 2021–2026 Sportster S motorcycles due to upper triple clamp fracture risk.
FDA•MODERATEsmart & simple Turmeric PelletsSmartPak Equine is recalling smart & simple Turmeric Pellets due to elevated aflatoxin levels.
NHTSA•MODERATEOshkosh NGDV Brake Pedal Mounting Pin and Retaining ClipOshkosh is recalling 2025–2026 NGDV vehicles; brake pedal mounting pin and retaining clip may be missing, risking brake failure.
FDA•MODERATEValley Springs 100% Natural Bottled WaterValley Springs is recalling 100% Natural Bottled Water in 1 Gal jugs due to insanitary bottling conditions.
4 products
FDA•MODERATEArtelon FlexBand Dynamic MatrixInternational Life Sciences is recalling the Artelon FlexBand Dynamic Matrix due to failure to meet bacterial endotoxin testing requirements.
3 products