Device Recall
FDA•MODERATE
B. Braun CESK Northside Anesthesia Tray
B. Braun recalls CESK Northside Anesthesia Tray due to cracked adhesive tubing.
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FDA•MODERATECovidien Mon-a-Therm Esophageal StethoscopeCovidien recalls Mon-a-Therm Esophageal Stethoscope 400TM (REF 90042) due to lack of FDA clearance.
3 products
FDA•MODERATEExacta Mix Vented Micro-Volume InletBaxter is recalling Exacta Mix Vented Micro-Volume Inlet (Model H938175) due to incorrect filters that may cause flow and clinical issues.
FDA•CRITICALBD Spinal Tray with Quincke NeedleBD recalls Spinal Tray with Quincke Needle over quality issues in bupivacaine component.
10 products
FDA•MODERATECovidien Shiley Tracheostomy TubeCovidien is recalling Shiley Tracheostomy Tubes due to incorrect display box labeling.
FDA•MODERATEIvenix Infusion System Large Volume PumpFresenius Kabi is recalling the Ivenix Infusion System LVP due to a risk of the cassette loading lever breaking during use.
CPSC•Giantex and Costway Portable Steam SaunasThe steam diffuser can be positioned too close to the user, allowing hot steam to come into contact with the body.
CPSC•MiniWarGaming and Primal Horizon Disc MagnetsThese magnets pose a serious ingestion hazard to children, as they can attract each other or other metal objects if swallowed, potentially causing intestinal perforation, blockage, or death.
CPSC•Zen Magnetic Promotional Ball SetsZen magnetic ball sets are recalled due to a severe ingestion hazard that violates federal toy safety standards.
CPSC•Giantex Outdoor Lounge ChairsGiantex is recalling model NP10025NY outdoor lounge chairs due to a pinch point that poses an amputation risk to consumers.
CPSC•Joy Furniture Talan and Royce Living Room SetsJoy Furniture is recalling Talan and Royce living room sets due to a fire hazard caused by malfunctioning power switches.
CPSC•Panasonic Lithium Coin BatteriesPanasonic VL2020 lithium coin batteries are recalled for lacking child-resistant packaging, posing a severe ingestion and chemical burn risk.
CPSC•Anzmtosn Luminous Fidget Spinner BallsAnzmtosn is recalling Luminous Fidget Spinner Balls (Model FS0862) because the included flashlight batteries pose a serious ingestion hazard.
CPSC•Misco Sports Light-Up Racket SetsMisco Sports Light-Up Racket Sets (model MT2287) are recalled due to a battery ingestion hazard that can cause serious injury or death.
CPSC•Tzumi Electronics Sauna BlanketsTzumi Electronics is recalling SLF Sauna Blankets (model 30065TAR) due to overheating, which poses fire and burn hazards.
CPSC•Mainstays 9-Drawer Fabric DressersMainstays 9-Drawer Fabric Dressers are recalled due to tip-over and entrapment hazards that violate federal safety standards.
FDA•MODERATEGE HealthCare CARESCAPE Telemetry ServerGE HealthCare recalls CARESCAPE Telemetry Server V5 ATO over potential loss of ECG and SpO2 monitoring.
6 products
FDA•MODERATEMedtronic 1x4 Pocket Adaptor KitMedtronic recalls 1x4 Pocket Adaptor Kit (Model 64001) due to incorrect Use-By-Dates.
2 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.
FDA•CRITICALMedline Anesthesia Trays with Huons BupivacaineMedline recalls anesthesia trays with Huons bupivacaine over quality and efficacy issues.
10 products
FDA•MODERATEPhilips Azurion System HDDPhilips recalls Azurion systems over aging HDDs that may cause loss of imaging or movement.
3 products
FDA•CRITICALDark Chocolate Coconut Almond BitesBazzini recalls Dark Chocolate Coconut Almond Bites over undeclared peanuts.
FDA•CRITICALD'Dioses Fruit Pops: multiple undeclared allergens32 D'Dioses Fruit Pops products recalled for undeclared tree nuts or milk.
32 products
FDA•MODERATEHydroMARK Breast Biopsy Site MarkerDevicor Medical is recalling HydroMARK breast biopsy site markers due to incorrect inner package labeling.
FDA•CRITICALOmnipod 5 PodsInsulet recalls Omnipod 5 Pods over cannula damage causing insulin leaks and under-delivery, risking DKA.
3 products
FDA•CRITICALTNVitamins and Doctor's Pride Moringa CapsulesTotal Nutrition is recalling TNVitamins and Doctor's Pride Moringa capsules due to potential Salmonella contamination.
FDA•MODERATEDexcom G7 Continuous Glucose Monitoring SystemDexcom is recalling stolen G7 sensors that were meant for destruction, posing risks of infection, sensor failure, and inaccurate readings.
FDA•CRITICALMogo Pure Moringa Oleifera CapsulesMogo Moringa is recalling Pure Moringa Oleifera Capsules due to potential Salmonella Typhimurium contamination.
- Food RecallFDA•CRITICALRaaw Energy: possible Listeria contamination
37 Raaw Energy products recalled for possible Listeria.
37 products 
FDA•CRITICALSKS Copack: 19 productsSKS Copack recalls Boba Time and Angel drink powders over possible Salmonella contamination.
19 products
FDA•MODERATEToxiBan Charcoal-Kaolin SuspensionLloyd is recalling ToxiBan Charcoal-Kaolin Suspension for domestic animals due to microbial levels exceeding specification limits.
FDA•CRITICALMy Pet Carnivore Coarse Ground Whole GoatMy Pet Carnivore Coarse Ground Whole Goat is recalled due to potential Listeria monocytogenes contamination.
8 products
FDA•CRITICALHoneyville Banana Smoothie MixHoneyville is recalling bulk Banana Smoothie Mix due to potential Salmonella contamination in an ingredient.
FDA•MODERATEHalyard Purezero Ultraviolet Nitrile Exam GlovesHalyard is recalling Purezero Ultraviolet Nitrile Exam Gloves due to a failure to meet chemical permeation performance specifications.
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•CRITICALBolton Medical Thoracic Stent-Graft Delivery SystemBolton Medical Inc. is recalling its Thoracic Stent-Graft delivery system due to a labeling update concerning disconnection of the proximal clasp from the outer control tube, which may prevent release of the stent-graft from the delivery system.
2 products
FDA•CRITICALWhole Foods Market Kitchens Minestrone SoupWhole Foods Market Kitchens Minestrone Soup is recalled due to an undeclared shrimp allergen.
CPSC•ABC Trading Children's ToysABC Trading is recalling toy headbands and electronic pet cages due to a button cell battery ingestion hazard posing a risk of death.
CPSC•WSDZ LED Shot GlassesWSDZ LED shot glasses are recalled due to a battery ingestion hazard that can cause serious injury or death.
CPSC•Bethlehem Lights 10-inch Illuminated Ribbon SpheresBethlehem Lights 10-inch Illuminated Ribbon Spheres are being recalled due to an overheating fire hazard that poses a risk of injury or death.
CPSC•Sierra 125U Youth ATVsSierra 125U youth ATVs are recalled for failing federal safety standards, posing crash, collision, and burn hazards.
CPSC•Orb Funkee Squeeze ToysOrb Funkee squeeze toys are recalled due to the presence of asbestos in their sand filling, posing a serious inhalation risk.
CPSC•PandaEar Portable Hook-On ChairsPandaEar is recalling portable hook-on chairs (models C2102 and BTC-51) due to a fall hazard caused by removable crotch restraints.
CPSC•HomeProGym Resistance BandsHomeProGym is recalling purple 60lb and gray 70lb resistance bands that can detach from the handle, posing an impact injury risk.
FDA•MODERATEFentanyl Citrate Sterile CADD for InjectionIntegraDose is recalling Fentanyl Citrate Sterile CADD for Injection (NDC 71139-6030-1) due to the product being subpotent.
FDA•MODERATENephronex Vitamin B-Complex, Vitamin C & Folic Acid LiquidSafecor Health is recalling Nephronex dietary supplement liquid due to the presence of foreign black particles.
FDA•CRITICALSolina U.S. Holding: 10 productsSolina recalls multiple seasonings over potential Salmonella contamination.
10 products
FDA•CRITICALFontana Flavors: 3 For Further Processing WisFontana Flavors recalls 3 flavor products (white cheddar, cream of mushroom, parmesan) over possible Salmonella.
3 products
FDA•MODERATEPhilips Azurion Image Guided Therapy SystemsPhilips is recalling various Azurion systems due to potential mechanical wear in the Float Tabletop control module affecting table movement.
2 products
FDA•MODERATEPhilips Azurion X-ray Tube Cooling Unit Deaeration HosePhilips recalls Azurion systems: deaeration hose may leak oil, causing cooling failure and low-dose fluoroscopy lockout.
4 products