BEUDAMED
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    U OF I STERNUM NEEDLE 15GA

    FDA Adverse Event
    Injury ·ALLEGIANCE HEALTHCARE CORPORATION·Product code FMI·August 18, 2000

    Philips 5-Lead Set, Disposable, Bedside, AAMI Model # 989803173131 Product Usage: Philips Single-Patient-Use ECG lead sets for bedside monitoring are available in 5-lead configuration

    FDA Enforcement
    Class II ·Terminated·Philips North America, LLC·September 18, 2019

    Abbott Point of Care i-Stat cTnI cartridge. The i-Stat cardiac troponin I (cTnI) test is an in vitro diagnostic test for the quantitive measurement of cardiac troponin I (cTnI) in whole blood or plasma. Measurements of cardiac troponin I are used in the diagnosis and treatment of myocardial infarction and as an aid in the risk stratification of patients with acute coronary syndromes with respect to the relative risk of mortality.

    FDA Enforcement
    Class II ·Terminated·Abbott Point of Care Canada Limited·January 30, 2013

    Abbott Point of Care, i-STAT E3+ Cartridge, (NA K Hct); List No: 06F08-01; Part No: 120500; Abbott Point of Care Inc., East Windsor, NJ 08520 USA; Product of Canada.

    FDA Recall
    Terminated ·Abbott Point of Care Inc.·Product code JGS·October 18, 2007

    Abbott Point of Care, i-STAT EC4+ Cartridge; (NA K Glu Hct); List No: 06F07-01; Part No: 121500; Abbott Point of Care Inc., East Windsor, NJ 08520 USA; Product of Canada.

    FDA Recall
    Terminated ·Abbott Point of Care Inc.·Product code JGS·October 18, 2007

    Abbott Point of Care, i-STAT CREA Cartridge (Creatine/Crea); List No: 06F10-01; Part No: 320100; Abbott Point of Care Inc., East Windsor, NJ 08520 USA; Product of Canada.

    FDA Recall
    Terminated ·Abbott Point of Care Inc.·Product code JGS·October 18, 2007

    Abbott Point of Care, i-STAT G Cartridge; (Glucose/Glu); List No: 06F09-01; Part No: 120100; Abbott Point of Care, Inc., East Windsor, NJ 08520, USA; Product of Canada.

    FDA Recall
    Terminated ·Abbott Point of Care Inc.·Product code JGS·October 18, 2007

    Abbott Point of Care, i-STAT 6+ Cartridge (Na K CL BUN/Urea GLU Hct); List No: 06F05-01; Part No: 121000; Abbott Point of Care Inc., East Windsor, NJ 08520 USA; Product of Canada.

    FDA Recall
    Terminated ·Abbott Point of Care Inc.·Product code JGS·October 18, 2007

    Abbott Point of Care, i-STAT EC8+ Cartridge; (NA K CL Glu pH PCO 2 UN/Urea Hct); List No: 06F04-01; Part No: 12500; Abbott Point of Care Inc., East Windsor, NJ 08520, USA; Product of Canada.

    FDA Recall
    Terminated ·Abbott Point of Care Inc.·Product code JGS·October 18, 2007

    EASYTOUCH

    FDA Adverse Event
    Malfunction ·BERPU MEDICAL TECHNOLOGY CO., LTD·Product code FMF·May 28, 2026

    i-STAT DE handheld data processing module for clinical use, Software Version 2.8, List Number:08K46-01115200 (UDI: 00054749001255)

    FDA Recall
    Terminated ·Abbott Point Of Care Inc.·Product code JQP·September 12, 2017

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·February 6, 2011

    Eclipse(TM) Treatment Planning System with Proton Convolution Superposition algorithm license only The Eclipse Treatment Planning System (Eclipse TPS) is used to plan radiotherapy treatments for patients with malignant or benign diseases. Eclipse TPS is used to plan external beam irradiation with photon, elec- tron and proton beams, as well as for internal irradiation (brachytherapy) treatments. In addition, the Eclipse Proton Eye algorithm is specifically indicated for planning proton treatment of neoplasms of the eye.

    FDA Enforcement
    Class II ·Terminated·Varian Medical Systems, Inc.·January 30, 2019

    Active I-PTH ELISA, Part Number: DSL-10-8000 The DSL-10-80000 ACTIVE I-PTH Enzyme-Linked Immunosorbent Assay (ELISA) Kit provides materials for the quantitative measurement of I-PTH in serum or plasma. This assay is intended for in vitro diagnostic use as an aid in the diagnosis of hyperparathyroidism.

    FDA Recall
    Terminated ·Beckman Coulter Inc.·Product code CEW·April 22, 2010

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON-IRVINE TECHNOLOGY CTR.·Product code HQE·November 3, 2005

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·January 6, 2011

    MAXPLUS TRI-FUSE EXTENSION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP.·Product code FPA·November 20, 2013

    Active I-PTH Enzyme-Linked Immunosorbent Assay(ELISA), Part Number: DSL-10-8000 The DSL-10-8000 ACTIVE I-PTH Enzyme-Linked Immunosorbent Assay (ELISA) Kit provides materials for the quantitative measurement of I-PTH in serum or plasma. This assay is intended for in vitro diagnostic use as an aid in the diagnosis of hyperparathyroidism

    FDA Recall
    Terminated ·Beckman Coulter Inc.·Product code CEW·March 4, 2010

    GC 10F 80CM VISTA BRITE

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DQY·February 4, 2010

    ENDO GIA II 60-4.8 SULU

    FDA Adverse Event
    Injury ·USSC PUERTO RICO·Product code GDW·July 13, 2011