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AMZCMJ DGD Children's Tower Stool
AMZCMJ DGD children's tower stools risk collapse, tipping, and child entrapment through side openings.
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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.
NHTSA•CRITICALREV Recreation Group Motorhome GeneratorREV is recalling 2026 Holiday Rambler motorhomes (Vacationer, Admiral, Flair, Fortis, Bounder) due to furnace-triggered unexpected generator operation risking carbon monoxide poisoning.
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.
FDA•CRITICALFrench Broad Chocolate Bette's Bake Sale BonbonsFrench Broad Chocolate is recalling Bette's Bake Sale bonbons due to undeclared walnuts caused by mislabeling in the tasting guide.
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•CRITICALPork King Good Onion & Sour Cream SeasoningPork King Good is recalling Onion & Sour Cream Seasoning due to potential Salmonella contamination in the milk powder ingredient.
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.
NHTSA•CRITICALWinnebago Ekko Motorhome TouchscreenWinnebago Ekko motorhomes (2022–2027) may have phantom touchscreen inputs that turn on the generator, risking carbon monoxide poisoning in enclosed spaces.
FDA•MODERATEBD PurPrep Sterile SolutionCareFusion is recalling BD PurPrep sterile solution applicators distributed nationwide due to potential contamination and sterility concerns.
2 products
FDA•CRITICALWN-976-782-1 Seasoning for Cheese SauceGivaudan Flavors Corp is recalling WN-976-782-1 Seasoning for Cheese Sauce due to an ingredient recalled by the supplier.
FDA•MODERATEBioFire Joint Infection PanelBioFire is recalling Joint Infection (JI) Panel test kits due to contamination that may lead to false positive results.
FDA•CRITICALEllsworth Sour Cream + Onion SeasoningPS Seasoning & Spices is recalling Ellsworth Sour Cream + Onion Seasoning due to potential Salmonella contamination from a supplier ingredient.
6 products
FDA•CRITICALFontana Flavors White Cheddar Cheese FlavorFontana Flavors is recalling 50 lb. bags of White Cheddar Cheese Flavor due to potential Salmonella contamination from a supplier ingredient.
3 products
FDA•CRITICALRelayPro Thoracic Stent-Graft SystemBolton Medical is recalling 100+ variants of the RelayPro Thoracic Stent-Graft System due to a potential delivery system release failure.
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•CRITICALHoneyville Banana Smoothie MixHoneyville is recalling bulk Banana Smoothie Mix due to potential Salmonella contamination.
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.