FDA•MODERATE
Dextroamphetamine/Amphetamine Extended-Release Capsules
Lannett is recalling 5 mg Dextroamphetamine/Amphetamine ER capsules due to a labeling mix-up where capsules contain immediate-release pellets.
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FDA•MODERATEAsclemed: Multiple Lidocaine Hcl InjectionsAsclemed recalls Accucaine kits and Lidocaine HCl Injection USP, 1% (10 mg/mL), 5 mL ampules due to lack of sterility assurance.
2 products
FDA•MODERATEA.T.S. 4000 TS Tourniquet Dual HoseZimmer Surgical recalls A.T.S. 4000 TS Tourniquet Dual Hose (Model 60-1812-101-00) due to sterility breach risk.
2 products
FDA•MODERATEGORE TAG Thoracic Branch EndoprosthesisW.L. Gore & Associates is recalling its GORE TAG Thoracic Branch Endoprosthesis due to a device defect.
2 products
FDA•MODERATEBard Acute Drainage TraysBard recalls acute drainage trays due to lidocaine ampoules made under deficient practices.
20 products
FDA•MODERATEMedline Gravity SetMedline is recalling gravity sets labeled "Not for Human Use" that were inadvertently shipped to the U.S. market.
FDA•MODERATESolar GI System Water PerfusionLaborie is recalling Solar GI System configurations due to moisture accumulation that may affect pressure measurement performance.
FDA•MODERATECovidien Shiley Disposable Decannulation PlugCovidien recalls Shiley Disposable Decannulation Plug over incorrect non-DEHP labeling; product contains 30-35% DEHP.
2 products
NHTSA•MODERATEJayco Heartland Cyclone Travel and Fifth Wheel TrailersJayco is recalling 2026 Heartland Cyclone trailers due to a missing inverter ground connection that poses fire and electrical shock risks.
NHTSA•MODERATEJayco Seismic Fifth Toy HaulersJayco is recalling 2026 Seismic fifth toy haulers due to a missing grounding connection that poses fire and electrical shock risks.
NHTSA•MODERATEAltec Service Body Inverter AC WiringAltec is recalling 2022-2026 Service Body vehicles due to a wiring defect that may cause a short circuit and increase the risk of fire.
NHTSA•MODERATENissan Leaf Rear Seat Belt RetractorsNissan is recalling 2026 Leaf vehicles because rear seat belt retractors may fail to properly secure child restraint systems.
NHTSA•MODERATEWarn Wireless Remote KitsWarn is recalling wireless remote kits (part numbers 90287 and 90289) that may cause unexpected winch movement, posing an injury risk.
2 products
FDA•MODERATEEunha Fisheries: 2 productsEunha Fisheries recalls Korean halibut and flounder sashimi due to undeclared wheat, soy, sesame, Yellow #5, and Blue #1.
2 products
FDA•MODERATEGlucagon Emergency KitLupin recalls Glucagon Emergency Kits due to a stability test failure that may impair emergency use.
3 products
FDA•MODERATEProvision Health: 2 Dietary Supplement PHF-CsPH Labs recalls Ocular Plus and Vista MAX supplements due to undeclared Yellow #5.
2 products
FDA•MODERATEGemcitabine InjectionHikma is recalling Gemcitabine Injection due to improper temperature storage.
FDA•MODERATEZeiss Intrabeam Spherical ApplicatorZeiss is recalling the 1.5 cm Intrabeam Spherical Applicator (REF 304534-6000-557) due to failure to meet manufacturing specifications.
FDA•MODERATESiemens ARTIS icono Ceiling SuspensionSiemens is recalling the ARTIS icono ceiling suspension (Model 11328100) because monitor attachment screws may loosen over time.
FDA•MODERATERayCare 2024A SP1 Oncology Information SystemsRaySearch recalls RayCare 2024A SP1 oncology software due to potential data loss in beam set delivery notes.
2 products- Device RecallFDA•MODERATEMedela ENFit Enteral Extension Set
Medela is recalling ENFit Enteral Extension Sets due to incorrect connectors that may cause delivery delays or misconnections.
FDA•MODERATEAccuray Cyberknife Xchange Robotic Collimator ChangerAccuray is recalling the Xchange Robotic Collimator Changer for the Cyberknife system due to a risk of the collimator falling from its housing.
FDA•MODERATEARTIS icono biplaneSiemens recalls ARTIS icono biplane over potential loss of movement after detector lift height adjustment.
3 products
FDA•MODERATEAccuray Cyberknife Xchange Robotic Collimator ChangerAccuray is recalling the Cyberknife Xchange Robotic Collimator Changer due to a risk of the component falling from its housing.
FDA•MODERATECRE Pro Wireguided DilatorBoston Scientific recalls CRE Pro Wireguided dilator due to potential sterile pouch breach.
12 products
FDA•MODERATEIntelliCuff Portable Cuff Pressure ControllerThe IntelliCuff pressure controller may fail to maintain cuff pressure due to a system leakage error, causing the motor to run continuously.
FDA•MODERATEPilling Wecksorb NeurospongesTeleflex is recalling Pilling Wecksorb Neurosponges and Neurosponge Strips due to potential out-of-specification levels of endotoxins.
2 products
FDA•MODERATEBaxter Adapter for Head PositioningBaxter is recalling the Adapter for Head Positioning due to a risk of the accessory becoming loose and moving during patient positioning.
NHTSA•MODERATEHonda Odyssey Rearview CameraHonda is recalling 2018-2020 Odyssey vehicles because water intrusion can cause the rearview camera to fail, increasing the risk of a crash.
NHTSA•MODERATEBMW and Mini Integrated Brake SystemBMW is recalling various 2023-2025 BMW, Mini, and Rolls-Royce vehicles due to an integrated brake system malfunction that increases crash risk.
2 products
NHTSA•MODERATEMopar HeadlightsChrysler is recalling Mopar headlights that may flicker or fail, reducing vehicle visibility and violating federal safety standards.
NHTSA•MODERATERam 1500 Headlight WiringChrysler is recalling 2026 Ram 1500 vehicles due to headlight wiring issues that may cause parking and daytime running lights to fail.
NHTSA•MODERATEHonda Pilot and Passport Rear Subframe BoltsHonda is recalling 2026 Pilot and Passport vehicles due to improperly tightened rear subframe bolts that may cause stability loss.
FDA•MODERATESynjardy XR TabletsBoehringer Ingelheim is recalling Synjardy XR tablets due to manufacturing deviations involving improper cleaning and sampling of production equipment.
FDA•MODERATELevothyroxine Sodium Tablets 300 mcgAccord Healthcare is recalling 300 mcg Levothyroxine Sodium Tablets due to subpotency.
FDA•MODERATEprednisoLONE Acetate Ophthalmic Suspension 1%Lupin Pharmaceuticals is recalling three sizes of prednisoLONE Acetate Ophthalmic Suspension 1% due to the presence of a foreign substance.
FDA•MODERATERemel GC Agar BaseRemel is recalling GC Agar Base plates due to a risk of reduced or no recovery of Neisseria gonorrhoeae strains.
NHTSA•MODERATEEntegra Accolade and Jayco Seneca MotorhomesJayco is recalling 2027 Entegra Accolade and Jayco Seneca motorhomes because missing dinette brackets may cause the seating to detach.
NHTSA•MODERATETeko Triumph, Turbo, and Trophy VehiclesTeko is recalling 2026 Triumph, Turbo, and Trophy vehicles because a missing alert system prevents them from making required pedestrian sounds.
NHTSA•MODERATEJATCO Automatic Transmission Control Valve AssemblyNissan is recalling JATCO automatic transmission control valve assemblies that may fail to correctly display the selected gear.
NHTSA•MODERATELincoln Nautilus Hybrid and Explorer HybridFord is recalling certain 2024-2027 Lincoln Nautilus Hybrid and 2025-2027 Explorer Hybrid vehicles due to a missing pedestrian warning sound.
NHTSA•MODERATEFord Mustang and Mustang GTD Windshield WipersFord is recalling 2024–2026 Mustang and 2025–2026 Mustang GTD vehicles because cold weather can cause windshield wiper and washer malfunctions.
NHTSA•MODERATEFord Mustang Mach-E Rear Differential Pinion ShaftFord is recalling 2021-2023 Mustang Mach-E vehicles due to a risk of rear differential pinion shaft fracture and potential loss of drive power.
NHTSA•MODERATENissan Rogue Instrument PanelNissan is recalling 2026 Rogue vehicles because the instrument panel may fail to display the gear selection, increasing the risk of a crash.
NHTSA•MODERATEJeep Grand Wagoneer Brake System Control ModuleChrysler is recalling 2026 Jeep Grand Wagoneer and Grand Wagoneer L vehicles due to a software error that may cause a loss of brake assist.
2 products
NHTSA•MODERATEJeep Grand Cherokee and Wagoneer Transmission IndicatorChrysler is recalling certain 2022-2024 Jeep Grand Cherokee and Wagoneer vehicles due to a software error affecting the gear selection indicator.
FDA•LOWFexofenadine Hydrochloride Tablets 180 mgOhm Laboratories is recalling 180 mg Fexofenadine Hydrochloride tablets due to failed impurities and degradation specifications.
FDA•MODERATEImuldosa (ustekinumab-srlf) InjectionAccord BioPharma is recalling Imuldosa (ustekinumab-srlf) 130 mg/26 mL injection vials due to a lack of assurance of sterility.
FDA•MODERATELe Chef Bakery: 2 productsLe Chef Bakery recalls Mini Tiramisu and Mini Italian Pastry Assortment due to undeclared Yellow #5.
2 products
FDA•MODERATEOribe Serene Scalp Densifying ShampooOribe Serene Scalp Densifying Shampoo recalled due to microbial contamination.