NHTSA•MODERATE
Ford Windshield Wiper Arms
Ford is recalling 2021–2023 Lincoln Navigator, Expedition, and 2022–2023 F-Series Super Duty trucks due to windshield wiper arm breakage.
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NHTSA•MODERATEFord Lincoln Aviator and Explorer HVAC SystemFord is recalling 2026 Lincoln Aviator and Explorer vehicles for HVAC system failure affecting windshield defrosting.
FDA•MODERATEJFE FRANCHISING: 7 productsJFE recalls Dumpling Party Trays and Loaded Dumpling Vegetable products over possible glass contamination.
7 products
FDA•MODERATETramadol Hydrochloride Tablets 50 mgAmneal is recalling 500-count bottles of Tramadol Hydrochloride 50 mg tablets due to an impurity found during stability testing.
FDA•MODERATECurosurf (poractant alfa) 240 mg Intratracheal SuspensionChiesi USA is recalling Curosurf 240 mg intratracheal suspension vials (NDC 10122-510-03) due to lack of sterility assurance.
FDA•MODERATESynthes VOLT Locking Screw TapSynthes recalls VOLT Locking and Cortical Screw Taps due to incorrect thread from a lot swap.
2 products
FDA•MODERATEOlympus SOLTIVE Laser SystemOlympus recalls SOLTIVE laser systems (TFL-SLS, TFL-PLS) due to power supply defect that may cause inoperability and smoke.
2 products
NHTSA•MODERATEAston Martin DBX Rear Lower Suspension ArmAston Martin is recalling 2021–2026 DBX models due to rear suspension arm pin failure risking loss of control.
NHTSA•MODERATETerex Pole Guide Arm Assembly PinTerex is recalling pole guide arm assembly pins (part 450543) due to cracked welds that may cause the arm to fall.
FDA•MODERATEVital Nutrients Aller-CVital Nutrients Aller-C is recalled due to undeclared egg, soy, and hazelnut allergens.
FDA•MODERATEOctreotide Acetate Injectable Suspension 20 mgTeva recalls Octreotide Acetate 20 mg vials over sterility assurance concerns.
6 products
FDA•MODERATEArtoura Breast Tissue ExpandersA recall was issued for Artoura Breast Tissue Expanders due to infusion sets that may contain dull or blunt needle tips.
7 products
FDA•MODERATEPhilips Allura Xper FD10/FD20 Wired Foot SwitchPhilips recalls Allura Xper FD10/FD20 systems over wired foot switch failure causing intermittent X-ray imaging.
22 products
FDA•MODERATEMedline ENFit G-Tube ConnectorMedline recalls ENFit G-tube connectors in care/discharge kits over seal failure and leakage risk.
2 products
FDA•MODERATEJiffy Original Composite Polisher Cups (Coarse)Ultradent is recalling Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011, due to crumbling and breakage risk.
FDA•MODERATESterile Radiology Procedure Kits Model DYNDH1491BMedline is recalling Sterile Radiology Procedure Kits Model DYNDH1491B due to potential sterile pouch packaging breach.
FDA•MODERATEStryker CHROMOPHARE Softlit Ring Surgical LightStryker is recalling the CHROMOPHARE Softlit Ring Surgical Light System due to a potential ceiling cover support failure.
FDA•MODERATEParadise Ultrasound Renal Denervation CatheterReCor Medical is recalling the Paradise Ultrasound Renal Denervation Catheter (Model PRDS-068-02) as these units were intended to be scrapped.
3 products
FDA•MODERATEVue Motion V12 Imaging SystemPhilips Vue Motion V12 (1017979) may display image frames out of sequence during dynamic imaging runs.
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.
NHTSA•MODERATELuxfer Gas Cylinder AdapterLuxfer is recalling gas cylinder adapters (model EP-O-350-8-U5) due to O-ring incompatibility risking hydrogen leak and fire.
2 products
NHTSA•MODERATEMercedes-Benz G580 Wheel BoltsMercedes-Benz is recalling 2025 G580 vehicles with incorrect wheel bolts that may loosen or detach.
NHTSA•MODERATEMercedes-Benz 2026 GLE/GLS Passenger Air BagMercedes-Benz is recalling 2026 GLE and GLS models over passenger air bag fabric defect that may prevent deployment.
NHTSA•MODERATEKTM 390 Duke and RC 390 Throttle Control UnitKTM is recalling 2022–2024 390 Duke and RC 390 motorcycles due to throttle control unit water ingress causing loss of power.
NHTSA•MODERATETriumph Trident 800 Headlight Low BeamTriumph is recalling 2026 Trident 800 motorcycles with improper headlight low beam illumination that increases crash risk.
FDA•MODERATEAtellica CH Enzymatic Hemoglobin A1c AssaySiemens is recalling the Atellica CH A1c_E assay due to a risk of depressed results when used alongside the RCRP assay on the same analyzer.
NHTSA•MODERATELucid Air Half-ShaftLucid is recalling 2024–2026 Air Pure RWD vehicles over half-shaft disconnection risk due to loose bolts.
NHTSA•MODERATEGillig Low Floor Transit Bus Federal PlacardGillig is recalling 2023–2024 Low Floor transit buses with Michelin X InCity Grip D tires due to GAWR placard exceeding tire load rating.
NHTSA•MODERATEChrysler Pacifica and Voyager Side Curtain Air BagsChrysler is recalling 2022–2026 Pacifica and Voyager vehicles for defective side curtain air bags that may fail to prevent ejection in a crash.
NHTSA•MODERATEVan Hool Bus Front Door Window GlazeABC BUS is recalling Van Hool buses (C2045, T2145, TX45, CX45, CX35) with incorrect door window glaze that may reduce visibility.
NHTSA•MODERATEHonda CB1000SP Fuel HoseHonda is recalling 2025 CB1000SP motorcycles due to fuel hose disconnection risk and potential fuel leak.
- Equipment RecallNHTSA•MODERATEMopar Side Curtain Air Bags
Chrysler is recalling Mopar side curtain air bags (part numbers 68224526AJ, 68224527AH) over insufficient pressure retention from sealed seams.
NHTSA•MODERATELucid Gravity Seat Belt Anchor BracketLucid is recalling 2025–2026 Gravity vehicles for defective second-row seat belt anchor brackets that may fail in a crash.
2 products
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.
FSIS•MODERATEBlackwing Organic Meats Beef and Pork ProductsFSIS alert: Blackwing Organic Meats beef and pork products made without inspection may contain undeclared allergens or bacteria.
8 products
FDA•MODERATEBrimonidine Tartrate/Timolol Maleate Ophthalmic SolutionApotex is recalling Brimonidine Tartrate/Timolol Maleate eye drops (NDC 60505-0589-1) due to lack of sterility assurance.
FDA•MODERATEOlympus PKS Cutting ForcepsOlympus recalls PKS Cutting Forceps over jaw breakage risk from defective welds.
7 products
FDA•MODERATEMICS3 Angled Sagittal Saw AttachmentHowmedica Osteonics is recalling the MICS3 Angled Sagittal Saw Attachment due to a risk of external screws loosening and detaching during use.
NHTSA•MODERATEVolvo VNL Brake Release DelayVolvo is recalling 2025–2026 VNL (4) trucks over delayed brake release that increases crash risk.
- NHTSA•MODERATEVolvo Trucks VNL Instrument Panel Display
Volvo Trucks is recalling 2025–2026 VNL (4) vehicles for instrument panel display failure that may hide speedometer and warning lights.
NHTSA•MODERATEVolkswagen Jetta and Taos Instrument PanelVolkswagen is recalling 2025 Jetta and Taos vehicles with instrument panels that may fail to display warning lights or gauges.
NHTSA•MODERATEAston Martin DBX Tire Pressure Monitoring SystemAston Martin is recalling 2025–2026 DBX and 2026 DBX S vehicles; TPMS warning light may not illuminate for low tire pressure.
FDA•MODERATEMangalm: 6 Product Of India OilsMangalm recalls Tops GOLD pickles (6 varieties) over erucic acid risk.
6 products
FDA•MODERATELevothyroxine Sodium Tablets USP 150 mcgMacleods Pharma recalls Levothyroxine Sodium 150 mcg tablets (NDC 33342-401-44) nationwide due to subpotency.
FDA•MODERATELantern Knee System Drill PlateThe Lantern Knee System drill plate is recalled due to a manufacturing error that may cause excessive bone cuts during surgery.
2 products
FDA•MODERATEMiniMed 780G Insulin PumpMedtronic is recalling MiniMed 780G insulin pumps (models MMT-1884, MMT-1886) over software defects that may cause inaccurate insulin delivery.
FDA•MODERATEStraumann Custom Abutment TiStraumann recalls Custom Abutment Ti for Straumann RC due to material mix-up.
2 products
FDA•MODERATETECNIS Eyhance IOL with Simplicity Delivery SystemAMO is recalling TECNIS Eyhance IOLs with Simplicity Delivery System (model DIB00) because the lens may fail to unfold properly.
2 products
FDA•MODERATEBiDop 3 Pocket DopplerKoven Technology is recalling the BiDop 3 Pocket Doppler due to unauthorized fetal indication labeling.
2 products
NHTSA•MODERATENova Bus LFS Transit Bus Seat BeltNova Bus is recalling LFS and LFS Artic transit buses (2016–2023) due to driver seat belt tension-relieving device failure.