FDA•MODERATE
Coconut Drink 1
HEYTEA USA INC is recalling Coconut Drink 1 (1L, UPC 673367992785) due to undeclared milk.
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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.
- Equipment RecallNHTSA•MODERATETerex Pole Guide Arm Assembly Pin
Terex is recalling pole guide arm assembly pins (part 450543) due to cracked welds that may cause the arm to fall.
FDA•MODERATEDisposable Mixing Bowls with SpatulaZimmer is recalling Disposable Mixing Bowls with Spatula (Model 00-5049-011-00) due to compromised sterile barrier seals.
FDA•MODERATEBoston Scientific LUX-Dx II Arrhythmia DetectorBoston Scientific is recalling LUX-Dx II arrhythmia detectors due to a software error that prevents proper monitoring and data collection.
2 products
FDA•MODERATEVital Nutrients Aller-C CapsulesBlueroot Health is recalling Aller-C capsules due to undeclared egg, soy, and hazelnut allergens.
FDA•MODERATEPrazosin Hydrochloride Capsules 1mgAppco Pharma is recalling Prazosin Hydrochloride Capsules 1mg due to the presence of N-nitroso-prazosin impurity above acceptable limits.
3 products
NHTSA•CRITICALYamaha TW200 SpeedometerYamaha is recalling 2026 TW200 motorcycles with speedometer failure that may increase crash risk.
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.
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•MODERATEMicro-X Rover Mobile X-ray GeneratorMicro-X is recalling the X-ray generator in Rover Mobile X-ray Systems due to a malfunction that can make the device inoperable.
FDA•CRITICALAIDBAG First Aid Kits with McKesson TRUE Metrix PRONorth American Rescue is recalling AIDBAG first aid kits with McKesson TRUE Metrix PRO glucose meters over E-5 error code software defect risking treatment delays.
2 products
FDA•MODERATEStraumann n!ce PMMA Full-arch RestorationStraumann is recalling n!ce PMMA Full-arch Restoration abutments (Article 010.0304) due to an incorrect screw seat interface.
2 products
FDA•MODERATEEdwards EVOQUE Tricuspid Delivery SystemEdwards Lifesciences is updating labeling for the EVOQUE tricuspid delivery system to include a warning about potential functionality issues.
FDA•MODERATEZarlengo's Double Dark Chocolate GelatoZarlengo's Double Dark Chocolate Gelato is recalled due to an undeclared soy allergen.
5 products
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•CRITICALNissan LEAF High Voltage Battery ModuleNissan is recalling 2026 LEAF vehicles over high voltage battery short-circuit fire risk.
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.
FDA•MODERATEEinstein Bros Bagels Honey Almond ShmearEinstein Bros Bagels is recalling Honey Almond Shmear mislabeled as Plain Cream Cheese due to an undeclared almond allergen.
FDA•MODERATEPantoprazole Sodium Delayed-Release Tablets 40 mgCamber Pharmaceuticals is recalling Pantoprazole Sodium 40 mg tablets (NDC 31722-713-10) due to discoloration.
FDA•MODERATEImmy Myco DDR Trident Neutralization Buffer BImmuno-Mycologics is recalling Myco DDR Trident Neutralization Buffer B due to potential contamination.
FDA•MODERATESpacelabs Ultraview SL Command ModuleSpacelabs is recalling the SL Command Module due to a manufacturing issue with the electrical leakage tester.
2 products
FDA•MODERATEGE Revolution CT SystemsGE is recalling Revolution CT systems due to a security vulnerability in the AW Server software used with the CT Smart Subscription feature.
7 products
FDA•MODERATEAlain Milliat Orange MarmaladeAlain Milliat Orange Marmalade is being recalled due to the potential presence of glass fragments in the product.
FDA•MODERATECrab CakesConnecticut Crab Company is recalling crab cakes sold to food service due to potential Clostridium botulinum contamination.
FDA•MODERATEGeri-Care Artificial Tears Lubricant Eye DropsGeri-Care Artificial Tears Lubricant Eye Drops (0.5 oz, NDC 68788-7266-0) recalled due to lack of sterility assurance.
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•MODERATEBombay Kitchen Tikka SevBombay Kitchen Tikka Sev is recalled due to undeclared FD&C Yellow #6 and FD&C Red #40 food dyes.
3 products
FDA•MODERATEFluocinonide 0.05% CreamTaro Pharmaceuticals is recalling Fluocinonide 0.05% Cream due to out-of-specification viscosity results.
3 products
FDA•LOWFarmina Pet Foods N&D Tropical Selection Dog FoodFarmina Pet Foods N&D Tropical Selection dog food (22 lb, UPC 8 01027 60423 85) recalled due to mislabeling—front lists salmon, back lists lamb.
FDA•MODERATEOxoid Salmonella 9-O Agglutinating SeraRemel Europe is recalling Oxoid Salmonella 9-O Agglutinating Sera due to potential cross-reactivity and misidentification risks.
FDA•MODERATEAvitene Ultrafoam Microfibrillar Collagen HemostatDavol is recalling Avitene Ultrafoam Microfibrillar Collagen Hemostat (Catalog 1050030) due to potential inspect fragment contamination.
FDA•MODERATEOlympus OER-ELITE Endoscope Reprocessor Connecting TubesOlympus is recalling OER-ELITE Endoscope Reprocessor Connecting Tubes (model MAJ-2110) due to potential premature failure of the lock levers.
12 products
FDA•LOWHeraeus PALAMIX uno Mixing SystemHeraeus is reducing the shelf life of PALAMIX uno mixing systems to 17 months due to a risk of the mixing rod detaching during use.
2 products
FDA•CRITICALVOCSN V+Pro Respiratory SystemVentec is recalling VOCSN V+Pro respiratory systems (REF: PRT-01198-000, PRT-01185-000) due to potential oxygen leaks that may increase fire risk.
FDA•MODERATEDEX Ophthalmic Tissue ForcepsKatalyst Surgical is updating the Instructions for Use for DEX Ophthalmic Tissue Forceps and 23ga DEX NanoTapered AWH Forceps.
12 products
FDA•MODERATEBioCera Fibers Bone Void FillerOrthorebirth is recalling BioCera Fibers bone void filler products that do not meet standard manufacturing specifications.
2 products
FDA•CRITICALOmnicell i.v.STATION Syringe Label StockOmnicell is recalling i.v.STATION syringe label stock due to the potential for mislabeled IV medication syringes.
FDA•MODERATEOmnipaque (iohexol) InjectionGE Healthcare is recalling Omnipaque (iohexol) injection due to the presence of particulate matter.
2 products