FDA•MODERATE
Covidien Mon-a-Therm Esophageal Stethoscope
Covidien recalls Mon-a-Therm Esophageal Stethoscope 400TM (REF 90042) due to lack of FDA clearance.
3 productsFilters
Category
Agency
Severity
Date
Distributed in
All Recalls
Back to home ←
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•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•MODERATEPhilips Azurion System HDDPhilips recalls Azurion systems over aging HDDs that may cause loss of imaging or movement.
3 products
FDA•MODERATEHydroMARK Breast Biopsy Site MarkerDevicor Medical is recalling HydroMARK breast biopsy site markers due to incorrect inner package labeling.
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.
- Food RecallFSIS•MODERATEOlympia Foods Beef Kofta
Olympia Foods beef kofta served at The Kebab Shop is under a public health alert due to potential E. coli O157:H7 contamination.
FDA•MODERATEToxiBan Charcoal-Kaolin SuspensionLloyd is recalling ToxiBan Charcoal-Kaolin Suspension for domestic animals due to microbial levels exceeding specification limits.
FDA•MODERATEHalyard Purezero Ultraviolet Nitrile Exam GlovesHalyard is recalling Purezero Ultraviolet Nitrile Exam Gloves due to a failure to meet chemical permeation performance specifications.
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•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
FDA•MODERATESilastic Foley CathetersC.R. Bard is recalling Silastic Brand Foley Catheters due to surface staining on the devices.
FDA•MODERATEEstradiol Gel 0.1%ANI Pharmaceuticals is recalling Estradiol Gel 0.1% due to defective packets that may be empty or partially full.
FDA•MODERATECimzia Prefilled SyringesUCB is recalling Cimzia prefilled syringes and starter kits due to a lack of assurance of sterility.
FDA•MODERATEErythromycin Tablets 250 mgZydus recalls Erythromycin 250 mg tablets due to impurity above acceptable limit.
2 products
FDA•MODERATEGlobus Medical OneLIF Integrated FixationGlobus Medical is recalling OneLIF integrated fixation systems because some units may not meet shelf-life specifications, which could affect product performance.
2 products
FDA•MODERATEMedtronic GUNDRY Retrograde CannulaMedtronic recalls GUNDRY Retrograde Cannula over sterile barrier breach risk.
9 products
FDA•MODERATEVitamin B-Complex, Vitamin C & Folic Acid SupplementLlorens Pharmaceuticals is recalling Vitamin B-Complex, Vitamin C & Folic Acid supplement bottles due to foreign black particulate matter.
FDA•MODERATEAllProvide Gently Cooked Chicken Recipe for DogsAllProvide is recalling 16 oz Gently Cooked Chicken Recipe for Dogs due to potential plastic contamination.
FDA•MODERATEGas-X Simethicone 125 mg SoftGelsHaleon is recalling Gas-X Simethicone 125 mg SoftGels (120 count), UPC 3 00674 35041 9, due to incomplete inactive ingredient labeling.
FDA•MODERATEWellnov Supplements: 14 Vitaminally LLC Chandler AzesWellnov recalls liquid multivitamins and supplements over cGMP deviations risking bacterial contamination and C. botulinum.
14 products
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•MODERATEAtomoxetine HCl CapsulesSafecor Health is recalling Atomoxetine HCl capsules due to a labeling mix-up that may result in patients receiving an incorrect dosage.
FDA•MODERATEICU Medical Oncology Extension SetICU Medical is recalling Oncology Extension Set REF: CL3960 due to a potential leak that could cause therapy interruption or hazardous exposure.
FDA•MODERATEOphthavet Ophthalmic SolutionDechra is recalling Ophthavet Ophthalmic Solution for dogs and cats due to a lack of sterility assurance.
FDA•MODERATETangent Single Use Digital CatheterTangent Endoscopy is recalling single-use digital catheters due to potential fractures at the distal shaft tip.
FDA•MODERATESwan-Ganz Catheters (Multiple Models)Becton, Dickinson and Company is recalling multiple variants of its Swan-Ganz pulmonary artery catheters due to a potential risk of valve leakage that may affect the balloon inflation performance.
3 products