NHTSA•MODERATE
Mack Pioneer and Anthem Rear Brake Modulator
Mack is recalling 2025–2027 Pioneer and 2026–2027 Anthem trucks over rear brake modulator short-circuit risk affecting ABS and stability control.
Filters
Category
Agency
Severity
All Recalls
Back to home ←
NHTSA•MODERATEVolvo VNR and VNL Rear Brake ModulatorVolvo is recalling 2025–2027 VNR and VNL trucks with rear brake modulators that may short circuit and disable ABS and stability control.
NHTSA•MODERATEJeep Wagoneer S and Dodge Charger Instrument Panel DisplayChrysler is recalling 2024–2025 Jeep Wagoneer S and Dodge Charger EVs for instrument panel display failure that may hide critical safety information.
NHTSA•MODERATELand Rover Defender Fuel TankLand Rover is recalling 2026 Defender vehicles with defective fuel tanks that may leak in a crash, posing a fire risk.
FDA•MODERATECalypso Tropic Tango LemonadeKing Juice is recalling Calypso Tropic Tango Lemonade (16 fl oz) due to undeclared Yellow No. 5.
CPSC•LOWLil Pick Up Rex110 and Sierra110 Youth ATVsLil Pick Up recalls 4,900 Rex110 and Sierra110 youth ATVs over crash hazard, suspension defects, and burn risk from hot footwell surfaces.
FDA•MODERATEEnalapril Maleate Tablets, USP 20 mgRising Pharma is recalling Enalapril Maleate 20 mg tablets (NDC 64980-688-10) due to failed impurities test.
NHTSA•MODERATEACDelco GMW DOT 3 Brake and Clutch FluidGM recalls ACDelco GMW DOT 3 brake fluid (lot #01977 091222) containing sediment that may reduce brake performance.
FDA•MODERATEJoint Nourish Liquid SupplementWellnov Supplements is recalling Joint Nourish liquid supplement due to potential bacterial contamination and C. botulinum concerns.
14 products
FDA•MODERATEOneLIF Interbody CageNovapproach Spine is recalling 60+ variants of OneLIF Interbody Cages due to a risk of inserter attachment failure during surgery.
2 products
FDA•MODERATESilastic Foley CathetersC.R. Bard is recalling Silastic Brand Foley Catheters due to surface staining on the devices.
FDA•MODERATECovidien Mon-a-Therm Esophageal StethoscopeCovidien is recalling Mon-a-Therm Esophageal Stethoscopes with Temperature Sensors because the devices lack FDA clearance.
3 products
FDA•MODERATEArvis Hip & Knee 3.0 Instrument Set ComponentsKico Knee Innovation is recalling Arvis Hip & Knee 3.0 instrument components over potential wear or corrosion on the magnet face.
2 products
FDA•MODERATESharpoint Microsurgical KnifeSurgical Specialties Corporation is recalling mislabeled Sharpoint microsurgical knives that contain 3.0mm blades instead of 2.2mm.
NHTSA•MODERATEToyota RAV4 Front Seat BracketsToyota is recalling 2025 RAV4 vehicles with improperly welded front seat brackets that may fail to restrain occupants in a crash.
NHTSA•MODERATERPM Freeride Recreational Trailer CooktopTrails West is recalling 2027 RPM Freeride trailers due to inverted cooktop flame fire risk.
NHTSA•MODERATEVolkswagen Taos Fuel Pressure SensorVolkswagen is recalling 2025–2026 Taos vehicles; fuel pressure sensor may dislodge in a crash, causing fuel leakage and fire risk.
NHTSA•MODERATETesla Cybertruck Wheel StudTesla is recalling 2024–2026 Cybertruck with 18-inch steel wheels over wheel stud separation risk.
FDA•MODERATEBD PurPrep Sterile SolutionCareFusion is recalling BD PurPrep sterile solution applicators distributed nationwide due to potential contamination and sterility concerns.
2 products
FDA•MODERATEBioFire Joint Infection PanelBioFire is recalling Joint Infection (JI) Panel test kits due to contamination that may lead to false positive results.
FDA•MODERATEExacta Mix Vented Micro-Volume InletBaxter is recalling Exacta Mix Vented Micro-Volume Inlets (Model H938175) due to incorrect filters that may cause clinical complications.
FDA•MODERATESystane Lubricant Eye GelAlcon is recalling Systane Lubricant Eye Gel due to a lack of assurance of sterility, which may impact product quality.
2 products
NHTSA•MODERATEHyundai Elantra and Tucson Air Bag SensorHyundai recalls 2025 Elantra N and 2026 Tucson models for misassembled air bag sensors that may delay deployment.
NHTSA•MODERATETern RC8 Digital Display ClusterHexagon Purus is recalling 2025–2026 Tern RC8 vehicles; digital display may show incorrect air brake pressure.
FDA•MODERATEWoodstock Organic Shelled EdamameWoodstock Organic Shelled Edamame (10 oz. and 48 oz.) recalled for metal pieces.
FDA•MODERATEDuloxetine Delayed-Release Capsules USP 60mgBreckenridge Pharmaceutical recalls Duloxetine 60mg capsules (NDC 51991-748-90) due to elevated N-nitroso impurity from manufacturing deviations.
FDA•MODERATEFrederik's by Meijer Vanilla Bourbon Trail MixFerris Coffee and Nut Company is recalling 9 oz bags of Vanilla Bourbon Trail Mix due to undeclared wheat and soy allergens.
FDA•MODERATEMedtronic GUNDRY Retrograde CannulaMedtronic is recalling GUNDRY Retrograde Cannula catheters due to a potential sterile barrier breach.
9 products
FDA•MODERATEMAC 5 Resting ECG Analysis SystemsGE is recalling MAC 5 A4 and A5 ECG systems due to a software error that may incorrectly associate clinical data with the wrong patient.
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•MODERATEOptase Dry Eye Intense DropsScope Health is recalling Optase Dry Eye Intense Drops (0.33 fl oz, NDC 72972-002-01) due to lack of assurance of sterility.
FDA•MODERATEMy Mochi Strawberry Non-Dairy Frozen DessertThe Mochi Ice Cream Company is recalling Strawberry Non-Dairy Frozen Dessert due to a foreign object found in a retail container.
FDA•MODERATENaproxen Oral Suspension USP 125 mg/5mLAcella Pharmaceuticals is recalling Naproxen Oral Suspension 125 mg/5mL (NDC 42192-619-16) due to lead and lithium contamination above specification.
FDA•MODERATEUncle Giuseppe's Marketplace Milk Chocolate Bridge MixUncle Giuseppe's Marketplace Milk Chocolate Bridge Mix is recalled for undeclared cashews, milk, and soy allergens.
FDA•MODERATEShimadzu Medical Systems X-Ray and Angiography GeneratorsShimadzu is recalling 20+ models of X-ray and angiography systems due to a contactor defect that may keep power active when switched off.
NHTSA•MODERATEGoodyear Eagle F1 Supersport TireGoodyear is recalling Eagle F1 Supersport tires (305/30ZR21, 255/35ZR20) over tread separation risk.
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•MODERATEFreshKote Lubricant EyedropsHarrow Eye LLC is recalling FreshKote Lubricant Eyedrops (0.33 fl oz) due to lack of assurance of sterility.
NHTSA•MODERATEMopar EngineChrysler is recalling Mopar engines (68364632CB, 68412483AF) over debris that may cause engine failure and fire.
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•MODERATENegita Cracker ShrimpHadson is recalling Negita Cracker Shrimp 2.8 oz over undeclared FD&C Yellow 6.
FDA•LOWLevocarnitine Injection, USP 1 g/5 mLAmerican Regent is recalling Levocarnitine Injection 1 g/5 mL vials (NDC 0517-1045-01) due to missing label.