BEUDAMED
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    Xoran MiniCAT CT Scanner ID ENT00001

    FDA Recall
    Terminated ·Xoran Technologies, Inc.·Product code JAK·December 14, 2009

    BD Pyxis MedFlex 2.0 REF 1139-00 Bio-ID Spare Parts REF 353200-01 The BD Pyxis" MedFlex is an Automated Dispensing Cabinet (ADC) intended to securely store and dispense medications and supplies to a qualified and authorized user in a clinical setting.

    FDA Recall
    Open, Classified ·CareFusion 303, Inc.·Product code BRY·January 23, 2025

    BD Phoenix PMIC/ID-105: IVD is intended for the in vitro rapid identification (ID) of gram-positive bacteria from pure culture belonging to the genera Staphylococcus, Enterococcus, and other gram-positive cocci and gram-positive bacilli Catalog Number: 448605 (Discontinued)

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code LON·December 8, 2020

    BD Phoenix PMIC/ID-108: IVD is intended for the in vitro rapid identification (ID) of gram-positive bacteria from pure culture belonging to the genera Staphylococcus, Enterococcus, and other gram-positive cocci and gram-positive bacilli Catalog Number: 448608

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code LON·December 8, 2020

    Hospitak Pediatric Manual Pulmonary Resuscitator with reservoir bag, face mask and Pop-Off 40 cm H2O Elbow. Product ID # 730-E; Hospitak Infant Manual Pulmonary Resuscitator with reservoir bag, face mask and Pop-Off 40 cm H2O Elbow, Product ID # 730MM.

    FDA Recall
    Terminated ·Unomedical·Product code BTM·October 6, 2009

    BD Phoenix PMIC/ID-107: IVD is intended for the in vitro rapid identification (ID) of gram-positive bacteria from pure culture belonging to the genera Staphylococcus, Enterococcus, and other gram-positive cocci and gram-positive bacilli Catalog Number: 448607

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code LON·December 8, 2020

    BD Phoenix PMIC/ID-109: IVD is intended for the in vitro rapid identification (ID) of gram-positive bacteria from pure culture belonging to the genera Staphylococcus, Enterococcus, and other gram-positive cocci and gram-positive bacilli Catalog Number: 448609

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code LON·December 8, 2020

    POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter with open suture holes, REF 5678300

    FDA Recall
    Completed ·Bard Peripheral Vascular Inc·Product code LJT·February 8, 2018

    POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter with Open Suture Holes, REF 1678301

    FDA Recall
    Completed ·Bard Peripheral Vascular Inc·Product code LJT·February 8, 2018

    POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter with open suture holes, REF 5678301

    FDA Recall
    Completed ·Bard Peripheral Vascular Inc·Product code LJT·February 8, 2018

    POWERPORT ClearVUE Slim with Smooth Septum, 6F ChronoFlex, Polyurethane Catheter with Open Suture Holes, REF 1676301

    FDA Recall
    Completed ·Bard Peripheral Vascular Inc·Product code LJT·February 8, 2018

    POWERPORT ClearVUE Slim with Smooth Septum, 6F ChronoFlex Silk, Polyurethane Catheter with Open Suture Holes, REF 5676301

    FDA Recall
    Completed ·Bard Peripheral Vascular Inc·Product code LJT·February 8, 2018

    POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter Custom Kit, REF CP00005

    FDA Recall
    Completed ·Bard Peripheral Vascular Inc·Product code LJT·February 8, 2018

    POWERPORT ClearVUE isp Implantable Port With Smooth Septum and Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter Custom Kit, REF CP00004

    FDA Recall
    Completed ·Bard Peripheral Vascular Inc·Product code LJT·February 8, 2018

    BD Phoenix" Panel NMIC/ID-123, Catalog # 448723, packaged 25 panels/carton, and labeled in part ***Becton, Dickinson and Company 7 Loveton Circle Sparks, MD 21152 USA (800) 638-8663*** The BD Phoenix Automated Microbiology System is intended for the rapid identification (ID) and antimicrobial susceptibility testing (AST) of clinically significant bacteria. The Phoenix system provides results for most aerobic and facultative anaerobic Gram negative bacteria of human origin with the use of the NMIC/ID-123 panel type.

    FDA Recall
    Terminated ·Becton Dickinson & Co. BD Diagnostic Systems·Product code LON·February 28, 2011

    Konica Minolta PrintLink III Model - ID/IV, code no. 0770, 0771 Medical Imaging Communication Device Model IV - product code 5000230 Model ID, product code 5000330 Konica Minolta Medical & Graphic, Inc. No. 26-2, Nishishinjuku 1-chrome, Shinjuku-ku, Tokoyo 163-0512, Japan

    FDA Recall
    Terminated ·Konica Minolta Medical Imaging USA, Inc.·Product code LMD·October 6, 2006

    Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID NOW COVID-19 2.0 24T Model/Catalog Number: 192-000 Software Version: N/A Product Description: Simple Point-Of-Care Device To Detect Sar-Cov-2 Nucleic Acid Targets Component: No

    FDA Recall
    Open, Classified ·Abbott Diagnostics Scarborough, Inc.·Product code QWR·March 4, 2025

    Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID NOW COVID-19 2.0 24T Model/Catalog Number: 192-000 Software Version: N/A Product Description: Simple Point-Of-Care Device To Detect Sar-Cov-2 Nucleic Acid Targets Component: No

    FDA Recall
    Open, Classified ·Abbott Diagnostics Scarborough, Inc.·Product code QWR·March 4, 2025

    ADVIA 560 Hematology Systems, Siemens Material Number (SMN) 11170842, IVD.

    FDA Recall
    Terminated ·Siemens Healthcare Diagnostics, Inc.·Product code GKZ·October 21, 2016

    Cytal Burn Matrix 10x15 cm. Product ID: BMM1015.

    FDA Recall
    Open, Classified ·Integra LifeSciences Corp. (NeuroSciences)·Product code KGN·March 19, 2026