NHTSA•MODERATE
Grand Design Lineage Solar Panel
Grand Design is recalling 2025–2026 Lineage RVs; solar panels may detach due to adhesive failure.
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NHTSA•MODERATENova Bus LFS Transit Bus Control UnitNova Bus is recalling 2022–2023 LFS transit buses; telemetry control unit may shut down and cause loss of drive power.
FDA•MODERATEOphthavet Ophthalmic SolutionDechra is recalling Ophthavet Ophthalmic Solution for dogs and cats due to a lack of sterility assurance.
FDA•MODERATEAtomoxetine HCl 10mg CapsulesSafecor is recalling Atomoxetine HCl 10mg Capsules (NDC 64380-474-01) because some cartons may contain 25mg capsules due to a labeling error.
FDA•MODERATEPhilips Azurion and Allura Imaging SystemsPhilips is recalling Azurion and Allura imaging systems due to hard disk drive failure that may cause loss of functionality or data.
2 products
FDA•MODERATEHiResolution Bionic Ear SystemAdvanced Bionics is recalling the HiRes Ultra 3D CI HiFocus Mid Scala cochlear implant due to an incorrect shelf-life expiration date.
FDA•MODERATEBD Pyxis MedStation 4000 Fingerprint ScannerCareFusion 303 is recalling the BD Pyxis MedStation 4000 medication cabinet due to a fingerprint scanner overheating burn risk.
8 products
NHTSA•MODERATENewmar Freedom Aire Front Chin SpoilerNewmar is recalling 2026 Freedom Aire motorhomes; front chin spoiler may detach during transit.
NHTSA•MODERATEDorman Transmission Gearshift CableDorman is recalling Transmission Gearshift Cables (part numbers 905-146, 905-644, 905-142, BK905-1146-1, BK905-1142-1) due to detachable bushing risking vehicle rollaway.
- NHTSA•MODERATENewmar 2026 Freedom Aire Motorhome Cargo Capacity Label
Newmar 2026 Freedom Aire motorhomes may have incorrect Cargo Carrying Capacity labels, risking overload and crash.
NHTSA•MODERATERoadtrek Recreational Vehicle Pop-Top LatchRoadtrek is recalling 2024–2026 Westfalia Wave SL, Zion Slumber, and other RV models due to pop-top latch disengagement risk during transit.
FDA•MODERATEDuloxetine Delayed-Release Capsules 30 mgAjanta Pharma is recalling Duloxetine Delayed-Release Capsules 30 mg due to the presence of an impurity exceeding FDA recommended limits.
3 products
NHTSA•MODERATEStoryteller Overland 2023 Coolant LinesStoryteller Overland recalls 2023 Stealth, Classic, and Beast Mode AWD vehicles for improperly routed coolant lines causing engine overheating.
FDA•MODERATEErythromycin 250 mg TabletsZydus is recalling Erythromycin 250 mg tablets due to CGMP deviations and the presence of an impurity above acceptable intake limits.
2 products
NHTSA•MODERATEJayco Granite Ridge and Entegra Condor Water Heater Mixing ValveJayco is recalling 2026 Granite Ridge and Entegra Condor motorhomes due to missing water heater mixing valve that could cause scalding.
NHTSA•MODERATEFord Ranger and Bronco Front Seat FrameFord is recalling 2024–2026 Ranger and Bronco vehicles over loose front seat frame bolts that may fail to restrain occupants in a crash.
NHTSA•MODERATELode-King Trailer Rear Impact GuardLode-King is recalling 2019–2026 SDG53-3, SDF53-3, and SDF50-3 trailers with defective rear impact guards that may not protect following vehicles in a crash.
NHTSA•MODERATEHarley-Davidson Motorcycle Airbox BaseplateHarley-Davidson is recalling 2024–2026 FLTRX, FLHX, FXBR, FLFB and other models with Airbox Baseplate 29000373 due to risk of pressurized oil ejection.
FDA•MODERATEProspector Popcorn Belgian Chocolate ToffeeProspector Popcorn Belgian Chocolate Toffee (UPC 850073852125) recalled for undeclared soy lecithin.
2 products
FDA•MODERATEPhilips Azurion Image-Guided Therapy SystemsPhilips is recalling various Azurion image-guided therapy systems due to mechanical wear that may impact table movement.
2 products- FDA•MODERATEPhilips Azurion X-Ray Tube Cooling Unit
Philips is recalling X-ray tube cooling units in Azurion systems due to hose degradation and potential oil leakage.
4 products 
NHTSA•MODERATEProliance High Voltage BatteryABS is recalling Proliance High Voltage Batteries (part 20000114-AB) due to contactor failure causing loss of drive power.
FDA•MODERATEOasis Tears PF Lubricant Eye DropsOasis Tears PF eye drops (NDC 42126-6400-1) recalled due to lack of assurance of sterility.
FDA•MODERATEMetoprolol Succinate Extended-Release Tablets 25 mgAscend Laboratories is recalling 25 mg Metoprolol Succinate Extended-Release Tablets due to failed dissolution testing.
FDA•MODERATEPhaseOne Antimicrobial Solution SprayerOculus Technologies is recalling PhaseOne Antimicrobial Solution due to sprayer spring corrosion that may contaminate the product.
FDA•MODERATECafe Nouria Blueberry MuffinThe Brownie Baker is recalling Cafe Nouria Blueberry Muffin due to undeclared walnuts, posing a risk to those with nut allergies.
FDA•MODERATEAligned Medical Fluids KitWindstone Medical Packaging is recalling the Aligned Medical AMS16835 Fluids Kit due to a supplier recall of the included Lidocaine injection.
FDA•MODERATEAmoxicillin and Clavulanate Potassium Oral Suspension DropsCronus Pharma is recalling Amoxicillin and Clavulanate Potassium oral suspension drops for dogs and cats due to product discoloration.
2 products- Vehicle RecallNHTSA•MODERATEUtilimaster Aeromaster Certification Label
Shyft is recalling 2022 Utilimaster Aeromaster vehicles with incorrect GVWR on certification label, risking overloading and crashes.
NHTSA•MODERATEAudi Q5 and SQ5 Seat BeltsAudi is recalling 2025 Q5 and SQ5 vehicles with defective driver and front passenger seat belts that may fail to restrain occupants.
FDA•MODERATEOctreotide Acetate Injectable Suspension 30 mgTeva is recalling Octreotide Acetate 30 mg injectable suspension kits (NDC 0480-9262-08) due to sterility assurance concerns from manufacturing deficiencies.
2 products
FDA•MODERATEGood & Gather Sesame Teriyaki Chicken with RiceGood & Gather Sesame Teriyaki Chicken with Rice is recalled due to undeclared sesame and soy allergens.
FDA•MODERATELiraglutide InjectionLupin is recalling Liraglutide Injection (NDC 70748-346-02 and 70748-346-03) due to white thread-like particulate matter in the cartridge.
FDA•MODERATEHydroMARK Breast Biopsy Site MarkerDevicor Medical is recalling HydroMARK breast biopsy site markers due to incorrect inner package labeling.
- Device RecallFDA•MODERATEGE HealthCare CARESCAPE Telemetry Server V5
GE HealthCare is recalling CARESCAPE Telemetry Server V5 units due to a risk of losing ECG and SpO2 monitoring capabilities.
6 products 
FDA•MODERATECASE v7.0 Cardiac Testing SystemGE Medical Systems is recalling the CASE v7.0 Cardiac Testing System due to a risk of electrical sparking and potential paper ignition.
FDA•MODERATEMedrad Avanta Injection System Tube SetsBayer is recalling Avanta Multi-Patient Administration Tube Sets due to a connection issue that may cause procedure interruptions.
FDA•MODERATEDa Vinci 5 NIR Handheld CameraIntuitive Surgical is recalling the da Vinci 5 NIR handheld camera system due to a risk of unintentional activation during surgery.
FDA•MODERATEiVIZIA Sterile Lubricant Eye DropsThea Pharma is recalling iVIZIA Sterile Lubricant Eye Drops due to a lack of assurance of sterility.
2 products
NHTSA•MODERATEMack Pioneer and Anthem Rear Brake ModulatorMack is recalling 2025–2027 Pioneer and 2026–2027 Anthem trucks over rear brake modulator short-circuit risk affecting ABS and stability control.
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.
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