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More INR Test Strips Recalled Due to Inaccurately High Results

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More INR Test Strips Recalled Due to Inaccurately High Results

December 21, 2018

More Blood-Pressure Drugs Recalled Due to Cancer-Causing Impurities

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More Blood-Pressure Drugs Recalled Due to Cancer-Causing Impurities

December 10, 2018

FDA Warns of Stroke and Arterial Dissection Risk With MS Drug

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FDA Warns of Stroke and Arterial Dissection Risk With MS Drug

November 29, 2018

FDA Touts Increased Oversight of Medical Device Makers

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FDA Touts Increased Oversight of Medical Device Makers

Michael O'Riordan

November 22, 2018

SORT-OUT IX: Statistical Mix-up Turns Trial’s Primary Endpoint Around

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SORT-OUT IX: Statistical Mix-up Turns Trial’s Primary Endpoint Around

Michael O'Riordan

November 06, 2018

INR Test Strips Recalled Due to Inaccurate Measurements

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INR Test Strips Recalled Due to Inaccurate Measurements

November 02, 2018

New Battery, Malfunction Issues Hit Beleaguered IABPs

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New Battery, Malfunction Issues Hit Beleaguered IABPs

November 01, 2018

FDA: Contaminated Irbesartan Now Under Voluntary Recall

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FDA: Contaminated Irbesartan Now Under Voluntary Recall

Michael O'Riordan

October 31, 2018

FDA: All AFX Endovascular AAA Systems Now Under Class I Recall

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FDA: All AFX Endovascular AAA Systems Now Under Class I Recall

October 16, 2018

FDA Warns of Deaths, Stroke With Latest-Generation Total Artificial Heart

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FDA Warns of Deaths, Stroke Due to Power System Problems With Total Artificial Heart System

August 17, 2018

FDA Recalls Valsartan-Containing Drugs After Detection of Carcinogen

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FDA Recalls Valsartan-Containing Drugs After Detection of Carcinogen

Michael O'Riordan

July 16, 2018

FDA Identifies Culprit in Endovascular Graft Type III Endoleaks

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FDA Identifies Culprit in Endovascular Graft Type III Endoleaks

June 19, 2018

Class I Recall for Medtronic’s HeartWare HVAD System

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Class I Recall for Medtronic’s HeartWare HVAD System

Michael O'Riordan

June 04, 2018

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HeartMate 3 Problem With Outflow Graft Twisting Called Class I Recall by FDA

May 23, 2018

FDA’s ‘Medical Device Safety Action Plan’ Focuses on Product Life Cycles and Preventing Cyberattacks

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FDA’s ‘Medical Device Safety Action Plan’ Focuses on Product Life Cycles and Preventing Cyberattacks

April 20, 2018

FDA: Battery, Cybersecurity Issues With ICDs and CRT-Ds Now Have Firmware Fix

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FDA: Battery, Cybersecurity Issues With ICDs and CRT-Ds Now Have Firmware Fix

April 17, 2018

Abciximab in ‘Short Supply’ Worldwide

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Abciximab in ‘Short Supply’ Worldwide

April 13, 2018

Manufacturing Defect Leads to Recall of Implanted Medtronic CRT-D Devices, ICDs

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Manufacturing Defect Leads to Recall of Implanted Medtronic CRT-D Devices, ICDs

February 27, 2018

Edwards Voluntarily Recalls Cardioband ‘Anchors’ Used in Mitral and Tricuspid Repair

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Edwards Voluntarily Recalls Cardioband ‘Anchors’ Used in Mitral and Tricuspid Repair

Michael O'Riordan

February 27, 2018

FDA: Clarithromycin Risks Persist in Patients With CAD

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FDA: Clarithromycin Risks Persist in Patients With CAD

February 26, 2018

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