23 results
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16ms
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Sources: EU EUDAMED, US FDA
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Status: Ongoing
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FoundationOne CDx (F1CDx), RAL-0003 version 31.0
FDA Enforcement
Class II
·Ongoing·Foundation Medicine, Inc.·December 3, 2025
FoundationOne Liquid CDx (F1LCDx), TECH-0009 version 6.0
FDA Enforcement
Class II
·Ongoing·Foundation Medicine, Inc.·December 3, 2025
FoundationOne Companion Diagnostic (F1CDx)
FDA Enforcement
Class II
·Ongoing·Foundation Medicine, Inc.·May 21, 2025
FoundationOne Companion Diagnostic (F1CDx)
FDA Enforcement
Class II
·Ongoing·Foundation Medicine, Inc.·June 11, 2025
FoundationOne Companion Diagnostic (F1CDx)
FDA Enforcement
Class II
·Ongoing·Foundation Medicine, Inc.·June 11, 2025
Torrent Suite Dx Software versions 5.14 and earlier used in connection with Ion PGM DX Systems-IVD intended for targeted sequencing of human genomic DNA (gDNA) from peripheral whole-blood samples and DNA and RNA extracted from formalin-fixed, paraffin-embedded (FFPE) samples. The Ion PGM Dx Instrument System is not intended for whole genome or de novo sequencing Product Name Installer /SKU /Updater SKU: (1) Torrent Suite Dx Software 5.14 -A52422/ A52417 (2) Torrent Suite Dx Software 5.12.5- A46166/ A46167 (3)Torrent Suite Dx Software 5.8- A36601/ A36602 (4)Torrent Suite Dx Software 5.6.4- A33178/ A33178 (5)Torrent Suite Dx Software 5.0- A29166/ A29166
FDA Enforcement
Class II
·Ongoing·Life Technologies Corporation·April 10, 2024
COOK MEDICAL Spectrum¿ Central Venous Tray: Reference Part Number C-UQLMYJ-1001J-RSC-ABRM-HC-FST-A-RD, Order Number G44800; Reference Part Number C-UTLMYJ-701J-ABRM-HC-IHI-FST-A-RD, Order Number G44809; Reference Part Number C-UTLMYJ-701J-RSC-ABRM-HC-FST-A-RD, Order Number G44806; Reference Part Number C-UTLMYJ-701J-RSC-ABRM-HC-IHI-FST-A-RD, Order Number G44807.
FDA Enforcement
Class II
·Ongoing·Cook Incorporated·April 15, 2026
ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER REF ASK-42802-PLH UDI code: (01)10801902133110(17)261231(11)251211(10)33F25L0140 REF ASK-45703-MGH UDI code: (01)10801902223675(17)261231(11)251209(10)33F25L0143 REF ASK-42854-MGH UDI code: (01)10801902223668(17)261231(11)251210(10)33F25L0144 REF ASK-45854-MGH UDI code: (01)10801902223699(17)261231(11)251209(10)33F25L0145 The Arrowg+ard technology is intended to provide protection against catheter-related bloodstream infections (CRBSIs). It is not intended to be used as a treatment for existing infections nor is it indicated for long-term use (> 30 days). Clinical effectiveness of the Arrowg+ard Blue Plus catheter in preventing CRBSIs compared to the original Arrowg+ard Blue¿ catheter has not been studied.
FDA Enforcement
Class II
·Ongoing·ARROW INTERNATIONAL, LLC·April 29, 2026
Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-21142-DMC UDI code: (01)10801902218930(17)270630(11)251211(10)33F25M0671 The MAC Multi-Lumen Central Venous Access Device with Arrowg+ard Blue technology permits short-term (<30 days) venous access and catheter introduction to the central circulation. It may be inserted into the jugular, subclavian, or femoral veins. The Arrowg+ard technology is intended to help provide protection against catheterrelated infections. Clinical data have not been collected that demonstrate the use of the Arrowg+ard antimicrobial surface in decreasing catheter-related infections for this device. It is not intended to be used as a treatment for existing infections, nor is it indicated for long-term use.
FDA Enforcement
Class II
·Ongoing·ARROW INTERNATIONAL, LLC·April 29, 2026
Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1 UDI code: (01)10801902159578(17)270531(11)251205(10)33F25M0011 The Arrowg+ard technology is intended to provide protection against catheter-related bloodstream infections (CRBSIs). It is not intended to be used as a treatment for existing infections nor is it indicated for long-term use (> 30 days). Clinical effectiveness of the Arrowg+ard Blue Plus catheter in preventing CRBSIs compared to the original Arrowg+ard Blue¿ catheter has not been studied
FDA Enforcement
Class II
·Ongoing·ARROW INTERNATIONAL, LLC·April 29, 2026
CareLink Clinic, REF: MMT-7350
FDA Enforcement
Class II
·Ongoing·Medtronic MiniMed, Inc.·December 3, 2025
The Access TSH (3rd IS) assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative etermdination of human thyroid-stimulating hormone (thyrotropin, TSH, hTSH) levels in human serum and plasma using the Access Immunoassay Systems. Measurements of thyroid stimulating hormone produced by the anterior pituitary are used in the diagnosis of thyroid or pituitary disorders. This assay is capable of providing 3rd generation TSH results. The DxI 9000 Access Immunoassay Analyzer is an in vitro diagnostic device used for the quantitative, semi-quantitative, or qualitative determination of various analyte concentrations found in human body fluids.
FDA Enforcement
Class II
·Ongoing·Beckman Coulter, Inc.·October 23, 2024
Arrow Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC, REF CDC-45854-P1A; catheter, intravascular, therapeutic, long-term greater than 30 days
FDA Enforcement
Class I
·Ongoing·ARROW INTERNATIONAL Inc.·October 11, 2023
Arrow ErgoPack Complete, Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC, REF CDC-42854- PCN1A; catheter, intravascular, therapeutic, long-term greater than 30 days
FDA Enforcement
Class I
·Ongoing·ARROW INTERNATIONAL Inc.·October 11, 2023
Arrow ErgoPack Pressure Injectable Arrowg+ard Blue Advance Three-Lumen PICC pre-loaded with Arrow VPS TipTracker Stylet, REF CDC-45563-TTS; catheter, intravascular, therapeutic, long-term greater than 30 days
FDA Enforcement
Class I
·Ongoing·ARROW INTERNATIONAL Inc.·October 11, 2023
Arrow ErgoPack, Pressure Injectable Arrowg+ard Blue Advance Two-Lumen PICC pre-loaded with Arrow VPS Precision Stylet, REF CDC-45552-VPS2; Catheter: Percutaneous Implanted Long-Term Intravascular Catheter Stylet: Diagnostic Intravascular Catheter
FDA Enforcement
Class I
·Ongoing·ARROW INTERNATIONAL Inc.·October 11, 2023
Kosmos on iOS impacting iOS, Model Numbers: P007639, P007944, software is part of a general-purpose diagnostic ultrasound system.
FDA Enforcement
Class II
·Ongoing·Echonous Inc·July 17, 2024
ADVIA Centaur Erythropoietin (EPO) Assay (100 Test)
FDA Enforcement
Class II
·Ongoing·Siemens Healthcare Diagnostics, Inc.·March 20, 2024
Atellica IM Erythropoietin (EPO) Assay (100 Test)
FDA Enforcement
Class II
·Ongoing·Siemens Healthcare Diagnostics, Inc.·March 20, 2024
Astral 100 and Astral 150 ventilators
FDA Enforcement
Class I
·Ongoing·ResMed Ltd.·November 1, 2023