NHTSA•MODERATE
Hyundai Elantra and Tucson Air Bag Sensor
Hyundai recalls 2025 Elantra N and 2026 Tucson models for misassembled air bag sensors that may delay deployment.
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NHTSA•MODERATETern RC8 Digital Display ClusterHexagon Purus is recalling 2025–2026 Tern RC8 vehicles; digital display may show incorrect air brake pressure.
NHTSA•MODERATEThomas Built SAF-T-LINER HDX2 Driver Seat Belt AnchorThomas Built SAF-T-LINER HDX2 (2026–2027) driver seat belt anchor may be improperly installed, risking restraint failure in a crash.
NHTSA•MODERATEForest River East to West College Avenue and Entrada FenderForest River is recalling 2026–2027 East to West College Avenue and Entrada RVs due to fender-to-tire contact risk.
- NHTSA•MODERATEThomas Built SAF-T-LINER HDX2 Driver Seat Belt Anchor
Thomas Built SAF-T-LINER HDX2 (2026–2027) driver seat belt anchor may be improperly installed, risking inadequate crash restraint.
NHTSA•MODERATEMitsubishi Outlander Liftgate Gas SpringMitsubishi is recalling 2014–2022 Outlander vehicles; liftgate gas springs may rupture or fail, causing unexpected drop.
NHTSA•MODERATEQ'Straint QRT-3 Wheelchair Restraint RetractorQ'Straint QRT-3 wheelchair retractors may fail to lock, risking wheelchair movement during transit.
FDA•MODERATEGentuity HF-OCT Imaging SystemGentuity is correcting HF-OCT Imaging System software (versions 21.11–23.3.13) to prevent inaccurate longitudinal measurements during imaging.
NHTSA•MODERATEGoodyear Eagle F1 Supersport TireGoodyear is recalling Eagle F1 Supersport tires (305/30ZR21, 255/35ZR20) over tread separation risk.
2 products
NHTSA•MODERATEAltec Digger Derrick and Aerial Device Front End RadarAltec is recalling 2025–2026 Digger Derrick and Aerial Device vehicles with improperly installed front radar that may cause unexpected brake activation.
NHTSA•MODERATEBlue Bird All American Transit Bus Windshield Wiper Blade AssemblyBlue Bird is recalling 2026 All American transit buses with loose windshield wiper blade retention nuts that may cause wiper failure and reduced visibility.
NHTSA•MODERATELand Rover and Jaguar DC-DC ConverterJaguar Land Rover is recalling certain 2019–2024 Range Rover, Discovery, F-Pace, and E-Pace models due to DC-DC converter failure causing loss of drive power and lighting.
NHTSA•MODERATEBlue Bird All American School Bus Windshield Wiper Blade AssemblyBlue Bird is recalling 2026–2027 All American school buses with loose windshield wiper blade fasteners that may reduce visibility and increase crash risk.
FDA•MODERATEClaravis (isotretinoin capsule, USP) 10 mgTeva is recalling Claravis 10 mg capsules (NDC 0555-1054-56, 0555-1054-86) due to out-of-specification Tretinoin impurity levels.
3 products
FDA•MODERATEMemantine Hydrochloride Extended-Release CapsulesMajor Pharmaceuticals is recalling 7 mg Memantine Hydrochloride Extended-Release Capsules due to failed dissolution specifications.
FDA•MODERATEPantoprazole Sodium Delayed-Release Tablets 40 mgCamber Pharmaceuticals is recalling Pantoprazole Sodium 40 mg tablets (NDC 31722-713-10) due to discoloration.
FDA•MODERATEMedline Namic GuidewiresMedline recalls Namic syringes, guidewires, and tubing due to rescinded 510(k) clearances.
28 products
FDA•MODERATEMedline Convenience Kits with 10mL Polycarbonate SyringesMedline is recalling convenience kits containing select 10mL polycarbonate syringes due to potential cracking or breakage of the syringe barrel and/or plunger, which could result in loss of sterility and potential patient infection.
21 products
FDA•MODERATELeadCare II Blood Lead Test KitsMagellan recalls LeadCare II blood lead test kits over false elevated results from certain micro-collection devices.
4 products
FDA•MODERATECUSA Clarity C7000 ConsoleIntegra LifeSciences is recalling CUSA Clarity C7000 Console (Software 2.1.1.909) due to unresponsive touch screen.
FDA•MODERATESoft-Vu Angiographic CatheterAngiodynamics recalls Soft-Vu Angiographic Catheters due to guidewire passage defect.
20 products
FDA•CRITICALMedline Namic Angiographic Control SyringesWindstone recalls kits with Medline Namic RA Syringes over risk of adapter unwinding, which may cause disconnection and serious injury.
NHTSA•MODERATEMopar EngineChrysler is recalling Mopar engines (68364632CB, 68412483AF) over debris that may cause engine failure and fire.
2 products
NHTSA•MODERATEAltec AM Series Aerial Device Emergency Stop SwitchAltec is recalling 2025–2026 AM Series Aerial Devices with inoperative emergency stop switches that fail to cut power.
NHTSA•MODERATE2026 Ram 2500 Pickup Electronic Stability ControlChrysler is recalling 2026 Ram 2500 Pickups with steering column control module defects that disable electronic stability control.
FDA•MODERATEDesmopressin Nasal Spray, USP 10 mcg/0.1 mLApotex is recalling Desmopressin Nasal Spray (NDC 60505-0815-0) due to defective bottle caps with missing or dislodged liners.
3 products
FDA•MODERATEMedline CENTURION Circumcision KitMedline is recalling CENTURION Circumcision Kit (CIT7050F) due to one lot distributed without sterilization.
FDA•MODERATEPhilips Spectral CT on RailsPhilips Spectral CT on Rails (Model 728334) requires a software update to address gantry positioning, message display, and menu option issues.
FSIS•CRITICALAjinomoto Fried Rice, Ramen, and Shu MaiThe recall includes a wide range of ready-to-eat and not-ready-to-eat items sold nationwide.
3 products
NHTSA•CRITICAL2026 Nissan Frontier Pro4X R Steering ComponentsRoush is recalling 2026 Nissan Frontier Pro4X R vehicles over loose or missing steering fasteners that may cause loss of control.
NHTSA•MODERATEWinnebago Suncruiser and Sunflyer Side ReflectorsWinnebago is recalling 2026–2027 Suncruiser and Sunflyer motorhomes with missing side reflectors, increasing crash risk.
NHTSA•MODERATEAudi E-Tron Brake PedalAudi is recalling 2019–2024 E-Tron and 2020–2024 E-Tron Sportback vehicles due to brake pedal detachment risk.
FDA•MODERATEEpinephrine Injection USP 1 mg/10mLInternational Medication Systems is recalling Epinephrine Injection 1 mg/10mL (NDC 76329-3318-1) due to lack of sterility assurance.
FDA•MODERATECytal Wound Matrix 2-Layer 5x5 cmCytal Wound Matrix 2-Layer 5x5 cm recalled over out-of-specification endotoxin results.
5 products
FDA•MODERATEReact Health PHOENIX 5L Oxygen ConcentratorReact Health PHOENIX 5L Oxygen Concentrator recalled due to devices not meeting quality specifications.
FDA•CRITICALB. Braun STREAMLINE Bloodline SetB. Braun recalls STREAMLINE bloodline sets for Dialog DR over arterial line air bubble risk.
6 products
FDA•MODERATEElegance Anterior Cervical PlatesClariance-SAS is recalling Elegance Anterior Cervical Plates due to the presence of burrs on the finished product.
2 products
NHTSA•MODERATEFord Maverick and Bronco Sport Engine Block HeaterFord is recalling 2025 Maverick and 2026 Bronco Sport vehicles with 1.5L/2.0L MPC engine block heaters that may overheat and cause fire.
2 products
NHTSA•MODERATEFord F-59 and F-53 Front Axle Hub AssemblyFord is recalling 2025–2026 F-59 and F-53 vehicles with missing front axle hub spindle nuts, risking wheel detachment and loss of control.
NHTSA•MODERATEFord F-150 Transmission Range SensorFord is recalling 2015–2017 F-150 vehicles for unexpected transmission downshift risk due to sensor signal loss.
NHTSA•MODERATEFord Bronco Transmission-Transfer Case JointFord is recalling 2021–2025 Bronco vehicles for transmission-transfer case misalignment that may cause loss of drive power or rollaway.
NHTSA•MODERATEFord Ranger Sun Visor Wiring HarnessFord is recalling 2024–2026 Ranger vehicles over sun visor wiring that may short and cause fire.
2 products
FDA•MODERATEHuons: Multiple Rx Only InjectionsHuons recalls injectable lidocaine, bupivacaine, and saline due to sterility concerns.
9 products
FDA•LOWIsland Kinetics: multiple gelsIsland Kinetics recalls hydrocortisone 1% gels (Remedy Gel, Skin Rehab, Essential Calming) due to subpotency.
3 products
FDA•MODERATEAlbuterol Sulfate Inhalation Solution 0.5%Nephron SC recalling Albuterol Sulfate Inhalation Solution (NDC 69374-330-05) due to illegible labeling.
NHTSA•MODERATEEntegra Ethos Seating Capacity LabelJayco is recalling 2025–2026 Entegra Ethos RVs with incorrect seating capacity labels that may result in unbelted passengers.
NHTSA•MODERATEHarley-Davidson Softail Rear Brake LineHarley-Davidson is recalling 2025–2026 Softail motorcycles (FLHC, FXBB, FXLRS, FXLRST) due to rear brake line contact with the BCM causing brake failure.
FDA•MODERATEFluocinonide 0.05% Cream 15gTaro recalls Fluocinonide 0.05% Cream 15g tubes due to out-of-spec viscosity.
3 products
FDA•MODERATEInstinct Plus Endoscopic Clipping DeviceWilson-Cook Medical is recalling the Instinct Plus Endoscopic Clipping Device due to a potential for the device to malfunction.
NHTSA•MODERATEKia Carnival Fuel Pipe ConnectionKia is recalling 2022–2026 Carnival vehicles for fuel leak risk at the fuel pipe connection.