FDA•MODERATE
HydroMARK Breast Biopsy Site Marker
Devicor Medical is recalling HydroMARK breast biopsy site markers due to incorrect inner package labeling.
Filters
Category
Agency
Severity
All Recalls
Back to home ←- 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
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.
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.
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
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.
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•CRITICALLow Heat Non-Fat Dried Milk PowderCalifornia Dairies is recalling 2,200 lb totes of non-fat dried milk powder due to potential Salmonella contamination.
3 products
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•CRITICALAbiomed Automated Impella ControllerAbiomed is recalling the Automated Impella Controller due to hardware issues that may cause motor control, startup, or power failures.
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.
FDA•CRITICALHeritage Animal Nutrition Medicated FeedHeritage Animal Nutrition is recalling 50 lb bags of medicated feed due to potential rumensin contamination.