NHTSA•MODERATE
Land Rover and Jaguar DC-DC Converter
Jaguar 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.
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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.
FDA•MODERATEPublix Bran FlakesPublix Bran Flakes are being recalled due to the potential presence of plastic foreign material.
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.
- Food RecallFDA•MODERATESilver Moon LP: 48 recalled products
48 Silver Moon LP products recalled over tree nuts, peanuts, milk, eggs, soy, wheat, sulfites, and other hazards.
48 products 
FDA•MODERATECovidien Shiley Tracheostomy TubeCovidien is recalling Shiley Tracheostomy Tubes (REF 6FEN) due to incorrect display box labeling.
FDA•MODERATECovidien EndoStitch Polysorb Single Use Loading UnitCovidien is recalling EndoStitch Polysorb loading units (models 170053 and 170071) due to a compromised sterile barrier.
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.
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.
FDA•LOWMonsel's Ferric Subsulfate Solution 8 mLPremier Dental Products is recalling Monsel's Ferric Subsulfate Solution 8 mL vials (NDC 48783-112-08) due to incorrect expiration date on the vial label.
FDA•MODERATEPhilips Achieva 1.5T MR Elastography SystemPhilips is recalling Achieva 1.5T MRE systems due to a software error that may cause inaccurate stiffness value measurements.
19 products
FDA•MODERATESpecially SELECTED Vanilla Creme BruleeLactalis Canada is recalling Specially SELECTED Vanilla Creme Brulee (3.6 oz) over possible glass contamination.
FDA•MODERATEDexcom G7 CGM iOS AppDexcom is recalling G7 CGM iOS app versions 2.9.0–2.11.2 due to a software defect that may delay glucose alerts and readings.
4 products
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•MODERATE52USA Strawberry Popping Boba52USA Strawberry Popping Boba is recalled for containing unapproved food colors including FD&C Yellow 5, Yellow 6, and Red 40.
6 products
FDA•LOWBuspirone Hydrochloride Tablets 5 mgUnichem is recalling 500-count bottles of Buspirone Hydrochloride Tablets, 5 mg, due to subpotency.
FDA•MODERATEPhysio-Control LIFEPAK DefibrillatorsPhysio-Control is recalling various LIFEPAK defibrillators due to missing documentation of required performance inspections.
FDA•MODERATELUCAS Chest Compression SystemJolife AB is recalling LUCAS 2, 3, and 3.1 chest compression systems due to missing service documentation.
2 products
FDA•MODERATESwad Orange Flavored Masala CandyRaja Foods is recalling Swad Orange Flavored Masala Candy due to undeclared FD&C Yellow 6.
2 products
FDA•MODERATEHalyard Purezero Ultraviolet Nitrile Exam GlovesHalyard is recalling Purezero Ultraviolet Nitrile Exam Gloves due to a failure to meet chemical permeation performance specifications.
NHTSA•MODERATEKia Carnival Fuel Pipe ConnectionKia is recalling 2022–2026 Carnival vehicles for fuel leak risk at the fuel pipe connection.
NHTSA•MODERATEGenesis Fuel Pipe ConnectionGenesis is recalling GV70, G90, G80, and GV80 models over fuel leak risk at pipe connection.
NHTSA•MODERATE2026 Bentley Bentayga Tire Placard LabelBentley is recalling 2026 Bentayga vehicles with incorrect tire placard weight capacity labels.
NHTSA•MODERATENissan Cube Driver Air Bag InflatorNissan is recalling 2009–2010 Cube vehicles; driver air bag inflator may detach during deployment.
FDA•MODERATECodman CerebroFlo EVD CatheterIntegra LifeSciences is recalling the CerebroFlo EVD Catheter due to out-of-specification endotoxin results.
FDA•MODERATEBard Dynamic Deca Steerable Electrophysiology CatheterStryker is recalling Bard Dynamic Deca Steerable Electrophysiology Catheters due to incomplete sterile packaging seals.
26 products
FDA•MODERATEMedline Eye Tray-LF Convenience KitMedline is recalling Eye Tray-LF kits containing mislabeled Cardinal Health syringes that may lead to incorrect insulin dosing.
FSIS•MODERATEQuality Meat Sky Ranch Marinated Beef and Pork ProductsSky Ranch Meat recalled marinated beef and pork products (1.5-lb containers, Dec 2025–Apr 2026) for undeclared sesame allergen.
4 products
NHTSA•MODERATEHonda Odyssey Side Air BagsHonda is recalling 2018–2022 Odyssey vehicles; side air bags may deploy unexpectedly due to software error.
NHTSA•MODERATEJeep Cherokee Brake System Control ModuleChrysler is recalling 2026 Jeep Cherokee vehicles for brake module failure that disables ABS and electronic stability control.
NHTSA•MODERATEThomas Built Saf-T-Liner C2 Warning Lights and Stop SignThomas Built Saf-T-Liner C2 school buses (2024–2027) may lose warning lights and stop sign due to door switch software defect.
NHTSA•MODERATEIC Bus EVSB School Bus High Voltage Disconnect SwitchInternational is recalling 2022–2027 IC Bus EVSB school buses; high voltage disconnect switch may fail to cut power.
NHTSA•MODERATEJeep Wrangler Child Seat Tether WeldsChrysler is recalling 2026 Jeep Wrangler vehicles over insufficient child seat tether welds that may reduce crash restraint.
NHTSA•MODERATENova Bus Ricon Hidden Frame WindowsNova Bus is recalling Ricon hidden frame windows due to inadequate adhesion that may cause glass detachment during a crash.
NHTSA•MODERATERam 1500/2500/3500/4500/5500 Instrument Panel DisplayChrysler is recalling 2025–2026 Ram 1500/2500/3500/4500/5500 vehicles over instrument panel display failure that hides critical safety information.
NHTSA•MODERATEEnovation Controls PowerView 700 DisplayAkron Brass is recalling PowerView 700 displays (part numbers 610-00060-080-ST/080) that may fail to power on, preventing activation of emergency lights and equipment.
FDA•MODERATEOmega-3-Acid Ethyl Esters Capsules 1 gramMajor Pharmaceuticals is recalling Omega-3-Acid Ethyl Esters Capsules 1 gram (NDC 0904-7495-06) due to failed capsule shell specifications.
FDA•MODERATEThermedx FluidSmart Urology Tube SetStryker is recalling the FluidSmart Urology Tube Set due to the distribution of nonconforming products.
NHTSA•MODERATELexus RC, GS, IS Fuel PumpToyota is recalling 2015–2022 Lexus RC, 2016–2020 GS, and 2022 IS vehicles over fuel pump failure risk.