NHTSA•MODERATE
Ford F-Series Super Duty High Pressure Fuel Pump
Ford is recalling F-Super Duty F250–F550, F600, and F750 vehicles over high pressure fuel pump failure risk due to biodiesel deposits.
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NHTSA•MODERATETiffin Motorhomes GT1, GH1, GH2 Seating Capacity LabelTiffin is recalling 2025–2026 GT1, GH1, and 2026 GH2 motorhomes with incorrect seating capacity labels that may result in unbelted passengers.
NHTSA•MODERATEFord F-59 and F-53 Brake LightsFord is recalling 2025–2026 F-59 and F-53 chassis vehicles; brake lights may remain illuminated when not braking, increasing crash risk.
NHTSA•MODERATEForest River Entourage Motorhome CCC LabelForest River is recalling 2025–2026 Entourage motorhomes with incorrect CCC labels stating 7 belted seats instead of 8, risking overload and crashes.
FSIS•MODERATETurkey Stuffed PastriesShaw Bakers alerts on frozen turkey stuffed pastries mislabeled; some contain ham and cheese instead.
FDA•MODERATESimply Nature Spinach BitesDr. Praeger's is recalling Simply Nature Spinach Bites (12 oz) due to possible rodent hair contamination.
FDA•MODERATEChildren's Ibuprofen Oral Suspension 100 mg/5mLTaro Pharmaceuticals is recalling Children's Ibuprofen Oral Suspension 100 mg/5mL (120 mL) due to gel-like masses and black particles.
FDA•LOWPitavastatin Tablets, 2 mgNorthstar Rx LLC is recalling Pitavastatin Tablets, 2 mg (NDC 72603-479-01) due to a foreign 1 mg tablet found in bottles.
- Device RecallFDA•MODERATECentricity Universal Viewer Software
GE recalls Centricity Universal Viewer software over credential exposure risk.
4 products 
NHTSA•MODERATEOrange EV Terminal Truck Training SeatOrange EV is recalling T-Series, e-TRIEVER, and HUSK-e terminal trucks with foldaway training seats that may fail to restrain occupants in a crash.
2 products
NHTSA•MODERATEFerrari 12Cilindri WindowsFerrari is recalling 2025–2026 12Cilindri vehicles with dark-tinted windows that reduce driver visibility and fail safety standards.
FDA•MODERATEID NOW Influenza A & B 2 Test KitAbbott is recalling ID NOW Influenza A & B 2 test kits (Model 427-000) due to an increased rate of invalid results.
NHTSA•MODERATEMicro Bird G5 Transit Bus Wheelchair Tie-DownMicro Bird is recalling 2026 G5 transit buses with wheelchair tie-downs that may not lock due to installation error.
NHTSA•MODERATEAltec Service Body and Aerial Device VehiclesAltec is recalling 2023–2026 Service Body and Aerial Device vehicles with incorrect tire pressure labels that may cause blowout or crash.
NHTSA•MODERATEMicro Bird Transit Bus Wheelchair Tie-DownMicro Bird is recalling MB II, G5, and T-Series transit buses with wheelchair tie-downs that may not lock due to installation error.
NHTSA•MODERATENew Flyer Transit Bus Accelera ELFA 3 Control SystemNew Flyer is recalling XE35, XE40, XE60, XHE40, and XHE60 transit buses with Accelera ELFA 3 control systems over unintended acceleration/deceleration risk.
NHTSA•MODERATEMicro Bird School Bus Wheelchair Tie-DownMicro Bird is recalling MB II, G5, and T-Series school buses (2003–2026) with wheelchair tie-downs that may not lock due to installation error.
NHTSA•MODERATECummins PD7000 Electric Drive System Control ModuleCummins PD7000 Electric Drive (part BES CM0904 EV104B) recalled for SCM software error causing unintended vehicle movement.
NHTSA•MODERATENissan Kicks and Sentra Front Seat FrameNissan is recalling 2026 Kicks and Sentra vehicles with insufficiently welded front seat frames that may loosen during a crash.
2 products
FDA•MODERATEMedline Cardiac Procedure KitsMedline is recalling cardiac procedure kits to clarify that the included chest drainage units are intended for adult patients only.
FDA•MODERATEMedline Medcrest Surgical GownsMedline is recalling Medcrest surgical gowns due to fabric delamination risks that may lead to infection or delays in patient care.
3 products
FDA•MODERATELutronic CLARITY II Laser SystemLutronic is recalling CLARITY II Laser System (Model 1110200210) due to sparking and burn hazard.
NHTSA•MODERATEHonda CMX300, CMX500, CL500 Handlebar Lock ScrewHonda is recalling 2023–2025 CMX300, CMX500, and CL500 motorcycles; handlebar lock screw may detach and interfere with steering.
NHTSA•MODERATERolls-Royce Cullinan Seat Belt WebbingRolls-Royce is recalling 2020–2026 Cullinan vehicles; loose bolts may damage rear seat belt webbing and reduce crash protection.
NHTSA•MODERATEGillig Low Floor Transit Bus Air Compressor Intake PipeGillig is recalling 2021–2026 Low Floor transit buses over air compressor intake pipe contacting fuel line, risking fuel leak and fire.
NHTSA•MODERATEJeep Wagoneer S Liftgate Hinge CoverChrysler is recalling 2024–2026 Jeep Wagoneer S vehicles; liftgate hinge cover may detach and create a road hazard.
NHTSA•MODERATEGillig Low Floor Transit Bus High Voltage CableGillig is recalling 2023–2026 Low Floor transit buses over high voltage cable overheat and fire risk.
FDA•MODERATECocos Wholesale and Imports: 2 productsCoco's Italian Market recalls Cannoli Making Kit and Fettuccini Alfredo for undeclared wheat and milk allergens.
2 products
FDA•MODERATETemozolomide Capsules 5mgRising Pharmaceuticals is recalling Temozolomide Capsules 5mg (NDC 16571-816-51) due to failed impurities and degradation specifications.
FDA•MODERATESemaglutide Injection 2 mg Multi-Dose VialsNew Life Pharma recalls semaglutide 2 mg vials over sterility concerns.
4 products
FDA•MODERATEAmnesteem Isotretinoin Capsules 40 mgMylan is recalling Amnesteem Isotretinoin 40 mg capsules (NDC 0378-6614-93) due to failed dissolution specifications.
FDA•MODERATESodium Iodide (I-131) Therapeutic Oral SolutionRadnostix is recalling Sodium Iodide (I-131) Therapeutic Oral Solution due to the presence of particulate matter.
FDA•MODERATEArtelon FlexBand Dynamic MatrixArtelon FlexBand Dynamic Matrix recalled over failed endotoxin testing.
3 products
FDA•MODERATEBeckman Coulter DxC 700 AU Chemistry AnalyzerBeckman Coulter recalls DxC 700 AU and AU5800 analyzers over software delay risk.
2 products- Device RecallFDA•MODERATEHealthCast Vital Sync Remote Patient Monitoring System
HealthCast is recalling Vital Sync software due to a failure to transmit or receive critical patient bedside monitor alarms.
2 products 
FDA•MODERATEEndoVive Safety PEG KitBoston Scientific is recalling EndoVive Safety PEG Kits due to compromised seals on the included antiseptic swabsticks.
NHTSA•MODERATEATC PL700 and PL750 Recreational TrailersATC is recalling 2023–2026 PL700 and PL750 trailers over carbon monoxide entering the cabin from generator exhaust.
NHTSA•MODERATEMack TerraPro Engine Control Unit SoftwareMack is recalling 2022–2027 TerraPro trucks; ECU software may allow engine start in gear, risking unexpected movement.
NHTSA•MODERATEVolkswagen Jetta Transmission Ground WireVolkswagen is recalling 2025–2026 Jetta vehicles over loose transmission ground wire fire risk.
NHTSA•MODERATEVolvo EX30 Seat Belt Warning SystemVolvo is recalling 2025–2026 EX30 and 2026 EX30CC vehicles over a faulty seat belt warning chime system.
NHTSA•MODERATEARBOC Spirit of Freedom/Mobility Rear ABS SystemARBOC is recalling 2018–2026 Spirit of Freedom/Mobility buses over rear ABS malfunction that increases crash risk.
FDA•MODERATELowes Foods Sour Cream and Onion Potato ChipsUncle Ray's recalls Lowes Foods sour cream & onion chips (8 oz) over inaccurate nutrition and undeclared MSG.
FDA•MODERATEEndo-Model Replacement PlateauEndo-Model Replacement Plateau is recalled due to a risk of bushing detachment from the screw shaft caused by longitudinal fractures.
13 products
FDA•MODERATEGEM Premier 5000 PAKInstrumentation Laboratory is recalling GEM Premier 5000 PAK cartridges due to errors that may cause ejection and delay patient results.
20 products
FDA•MODERATEPhysio-Control Infant/Child Defibrillator ElectrodesPhysio-Control is recalling infant/child defibrillator electrodes due to a risk of delamination that could impact therapy delivery.
2 products
FDA•MODERATEAPTUS 2.5 TriLock ScrewsMedartis is recalling APTUS 2.5 TriLock Screws (model A-5750.16/1) due to a mix-up with 2.8mm screws.
2 products
FDA•MODERATEVegetarian Chicken Flavor RamenPalmetto Gourmet Foods is recalling Vegetarian Chicken Flavor Ramen 3oz packages due to undeclared Yellow #5.
2 products
FDA•MODERATEEquinoxe Core Instrument KitExactech recalls Equinoxe Core Instrument Kit and Ergo Impactor Handle over missing cross-pin risk.
2 products
FDA•LOWC2O Coconut Water with Pulp 17.5 ozC2O Coconut Water with Pulp 17.5 oz recalled over incorrect outer box labeling omitting added sugar.
FDA•MODERATERaz Mobile Shower Commode ChairsRaz Design is recalling various mobile shower commode chairs due to a seat bracket issue that may pose a fall risk to users.
2 products