18 results · 16ms · Sources: EU EUDAMED, US FDA

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In-vitro diagnostic kits: (1) Abbott Vysis MDM2 / CEP 12 FISH Probe Kit, REF 01N15-010; (2) Abbott Vysis LSI D13S319 (13q14.3) SpectrumOrange Probe, REF 01N34-020;

FDA Enforcement
Class III ·Ongoing·Abbott Molecular, Inc.·March 6, 2024

In-vitro diagnostic kits: (1) Abbott Vysis LSI ATM (11q22.3) SpectrmOrange Probe, REF 01N33-020; (2) Abbott Vysis PTEN/CEP 10 FISH Probe Kit, REF 04N62-020; (3) Abbott Vysis TelVysion 1p SpectrumGreen Probe, REF 05J03-001; (4) Abbott Vysis TelVysion 4P SpectrumGreen Probe, REF 05J03-004; (5) Abbott Vysis TelVysion 22q SpectrumOrange Probe, REF 05J04-022;

FDA Enforcement
Class III ·Ongoing·Abbott Molecular, Inc.·March 6, 2024

a) Alcon Custom-Pak CONSTELLATION 25G PLUS CHRISTIANA CARE HLTH SERV, # 15340-11, containing TUBING, SALEM SUMP, 14 FR; b) Alcon Custom-Pak DR GREEN VITRECTOMY MERCY HOSPITAL, # 6557-59 and # 6557-60 each containing TUBING, SALEM SUMP, 18 FR; c) VITRECTOMY ILLINOIS MASONIC MED CTR, # 9456-59, # 9456-60, and # 9456-61 each containing TUBING, SALEM SUMP, 18 FR; d) VITRECTOMY MCGEE EYE SURG CTR, # 12216-12, # 12216-14, and # 12216-15, each containing TUBING, SALEM SUMP, 14 FR.

FDA Enforcement
Class III ·Ongoing·Alcon Research LLC·November 27, 2024

The FastPack IP Sex Hormone Binding Globulin Immunoassay, Part #25000081, is for the quantitative measurement of SHBG in human serum and plasma. For in vitro diagnostic Use and contains 30 FastPacks.

FDA Enforcement
Class III ·Ongoing·Qualigen Inc·January 15, 2025

Platelet Aggregation Kit, Cat. No.5369, For use in platelet aggregation studies, Contains: 2X1 mL ADP Reagent containing adenosine diphosphate, 2X 1 mL Collagen Reagent containing collagen (equine tendon), 2 x 1 mL Epinephrine Reagent containing L-epinephrine, FOR IN-VITRO DIAGNOSTIC USE, Store at 2 to 8 C, 0011724/14(3)

FDA Enforcement
Class III ·Ongoing·Helena Laboratories, Corp.·December 4, 2019

HemosIL SynthAFax. Partial Thromboplastin Time Tests.

FDA Enforcement
Class III ·Ongoing·Instrumentation Laboratory·December 24, 2025

KWIK-STIK, ANA (3 Strains) QC Set, REF 5065P; Microbiological testing

FDA Enforcement
Class III ·Ongoing·Microbiologics Inc·September 20, 2023

Medica ISE Module Calibrant A; 500 mL - 140 mmol/L Na+, 125 mmol/L Cl-, buffers and preservatives; For use with ISE Module; Product Usage: Calibrations of ISE Model for integrated electrolyte system analysis.

FDA Enforcement
Class III ·Ongoing·AMS Diagnostics, LLC·July 19, 2017

Collagen Reagent, Cat. No. 5368, 2 X 1 mL, For use in platelet aggregation studies, Contains: Collagen (equine tendon) For In-Vitro Diagnostic Use,

FDA Enforcement
Class III ·Ongoing·Helena Laboratories, Corp.·December 4, 2019

VITROS Chemistry Products Performance Verifier II-For in vitro diagnostic use only.VITROS Chemistry Products Performance Verifier is an assayed control used to monitor performance on VITROS 250/350/5,1 FS/4600/XT 3400 Chemistry Systems and the VITROS 5600/XT 7600 Integrated System - Product Code: 8231474

FDA Enforcement
Class III ·Ongoing·Ortho Clinical Diagnostics Inc·November 25, 2020

RR Mechatronics Control Level A ESR Control4.6 ml QRR049002- In-vitro diagnostic quality control material to monitor the precision of Starrsed Erythrocyte Sedimentation Rate (ESR) instruments and procedures. Product Code: A0026578

FDA Enforcement
Class III ·Ongoing·Mechatronics USA·June 14, 2023

RR Mechatronics Starrsed Control Level N ESR Control 4.6 ml QRR049001- In-vitro diagnostic quality control material to monitor the precision of Starrsed Erythrocyte Sedimentation Rate (ESR) instruments and procedures. Product Code: A0026577

FDA Enforcement
Class III ·Ongoing·Mechatronics USA·June 14, 2023

Immunoassay Premium Level 3-In vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes. Catalog Number: IA2640

FDA Enforcement
Class III ·Ongoing·Randox Laboratories Ltd.·July 5, 2023

Full Dose CE Simplex P Single Bone Cement - Indicated for the fixation of prostheses to living bone in orthopaedic Catalog Number: 6191-0-001

FDA Enforcement
Class III ·Ongoing·Howmedica Osteonics Corp.·December 28, 2022

Immunoassay Premium Control Tri Level-In vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes Catalog Number: IA2633

FDA Enforcement
Class III ·Ongoing·Randox Laboratories Ltd.·July 5, 2023

NeuMoDx SARS-CoV-2 Assay -IVD intended for the qualitative detection of SARS-CoV-2 RNA from nasal, nasopharyngeal and oropharyngeal swabs in transport medium and bronchoalveolar lavage (BAL) specimens from individuals suspected of COVID-19 by their healthcare provider (HCP). REF Number: 300800

FDA Enforcement
Class III ·Ongoing·NeuMoDx Molecular Inc·July 12, 2023

ACE Control Set - IVD Control set for the quantitative determination of Angiotensin Converting Enzyme (ACE) REF 1667001

FDA Enforcement
Class III ·Ongoing·Sentinel CH SpA·July 14, 2021

VITROS Immunodiagnostic Products Vitamin B12 Range Verifier - In vitro diagnostic use ly. For use in verifying the calibration range of the VITROS ECi/ECiQ/3600 Immunodiagnostic Systems and the VITROS 5600/XT 7600 Integrated Systems when used for the quantitative measurement of vitamin B12 - Product Code: 6800872

FDA Enforcement
Class III ·Ongoing·Ortho-Clinical Diagnostics, Inc.·June 12, 2024