FDA•MODERATE
Oasis Tears PF Lubricant Eye Drops
Oasis Tears PF eye drops (NDC 42126-6400-1) recalled due to lack of assurance of sterility.
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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.
CPSC•AMZCMJ DGD Children's Tower StoolAMZCMJ DGD children's tower stools risk collapse, tipping, and child entrapment through side openings.
CPSC•TOETOL HOME Children's Tower StoolsTOETOL HOME tower stools (model DETD0001) can collapse or tip over, posing entrapment and fall hazards to children.
CPSC•Cpzzkq Baby LoungersCpzzkq baby loungers sold on Amazon pose suffocation risk; padding can obstruct infant breathing.
CPSC•KMUYSL Big Red Barn Farm Animal PlaysetsKMUYSL Big Red Barn Farm Animal Playsets (model SY-MZ7S-TVMV) recalled for detachable fence handles posing choking hazard to children under three.
CPSC•Magnetic Stick Figure SetsBlissfulDestiny magnetic stick figure sets recalled for loose magnets posing serious ingestion hazard to children.
CPSC•mGanna Sodium Hydroxide Pellet BagsmGanna Sodium Hydroxide pellet bags lack required child-resistant packaging, risking chemical burns and eye irritation.
CPSC•Autobrush Sonic Pro Kids Toothbrush BoxesAutobrush is recalling Sonic Pro Kids toothbrush boxes with accessible lithium coin batteries that pose serious ingestion hazards to children.
CPSC•32 Degrees Heated Socks32 Degrees heated socks (black, all sizes) recalled due to burn hazard during high-intensity activities.
CPSC•FitRx SmartBell Quick-Select Adjustable DumbbellsTzumi is recalling FitRx SmartBell dumbbells (model 8361) due to weight plates that can dislodge during use and cause serious injury.
CPSC•Sweetie Baby and Style Life Eleven Baby LoungersHappyGira recalls Sweetie Baby and Style Life Eleven baby loungers over fall and suffocation hazards violating infant sleep standards.
CPSC•Wiifo Children's Tower Stool Model LT005Wiifo tower stools (Model LT005) can collapse or tip, with side openings posing entrapment and fall risks to children.
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
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.