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News Industry News

Voluntary Recall of Fetch™ 2 Aspiration Catheter

April 11, 2016

News Daily News

FDA Tackles Regulatory, Scientific Issues With Point-of-Care Coagulation Monitoring Devices

Todd Neale

March 24, 2016

News Daily News

FDA Issues Class I Recall for Intra-Aortic Balloon Catheter and Percutaneous Insertion Kits

Michael O'Riordan

March 18, 2016

News Daily News

Good Guys, Bad Guys, or Just Big Money? The Push to Link Patient-Claims Data to Device Outcomes

Shelley Wood

March 17, 2016

News Daily News

MitraClip Manufacturer Issues Safety Notice on Proper Deployment

Caitlin E. Cox

February 28, 2016

News Daily News

FDA: Global Recall of Cook Medical Central Venous Catheters and Pressure Monitoring Sets, Trays

L.A. McKeown

February 10, 2016

News Opinion Conversations in Cardiology

Conversations in Cardiology: Post-PCI Clopidogrel in CHAMPION PHOENIX Trial of Cangrelor

February 08, 2016

News Daily News

ROCKET AF Investigators: Problems With Warfarin Monitoring Device Did Not Skew Results

Todd Neale

February 04, 2016

News Daily News

FDA Proposal Seeks to Shine Early Spotlight on Postmarket Device Safety Concerns

Caitlin E. Cox

January 03, 2016

News Daily News

FDA Warns of Class I Recall of Chariot Guiding Sheath Used in Peripheral Procedures

Shelley Wood

December 10, 2015

News Industry News

Voluntary Recall of Chariot™ Guiding Sheath

December 09, 2015

News Daily News

Path to Top FDA Post Gets a Bit Rockier for Califf

Michael O'Riordan

December 09, 2015

News Daily News

FDA: Class 1 Recall for Boston Scientific’s RotaWire Elite, WireClip Torquer Guidewires

Shelley Wood

November 29, 2015

News Daily News

FDA Warns of Potentially Serious Problems With Intravascular Device Coatings

Shelley Wood

November 22, 2015

News Daily News

Good News, Bad News Week for Watchman LAA Occluder

Shelley Wood

November 12, 2015

News Daily News

Quest Medical Voluntarily Recalls Models of Some Blood Pumps Used in Bypass Surgery

L.A. McKeown

October 29, 2015

News Industry News

Cook Medical Expands Global Recall of Select Sizes of Beacon Tip Angiographic Catheters

October 12, 2015

News Industry News

Cook Medical Issues Global Recall of Beacon Tip Angiographic Catheter Products

August 04, 2015

News Daily News

FDA Sounds Alarm Bells Over Use of Lariat Device for LAA Closure in A-fib Patients

Yael L. Maxwell

July 17, 2015

News Industry News

CloverSnare™ 4-Loop Vascular Retrieval Snare Recall

August 19, 2014

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Voluntary Recall of Fetch™ 2 Aspiration Catheter

FDA Tackles Regulatory, Scientific Issues With Point-of-Care Coagulation Monitoring Devices

FDA Issues Class I Recall for Intra-Aortic Balloon Catheter and Percutaneous Insertion Kits

Good Guys, Bad Guys, or Just Big Money? The Push to Link Patient-Claims Data to Device Outcomes

MitraClip Manufacturer Issues Safety Notice on Proper Deployment

FDA: Global Recall of Cook Medical Central Venous Catheters and Pressure Monitoring Sets, Trays

Conversations in Cardiology: Post-PCI Clopidogrel in CHAMPION PHOENIX Trial of Cangrelor

ROCKET AF Investigators: Problems With Warfarin Monitoring Device Did Not Skew Results

FDA Proposal Seeks to Shine Early Spotlight on Postmarket Device Safety Concerns

FDA Warns of Class I Recall of Chariot Guiding Sheath Used in Peripheral Procedures

Voluntary Recall of Chariot™ Guiding Sheath

Path to Top FDA Post Gets a Bit Rockier for Califf

FDA: Class 1 Recall for Boston Scientific’s RotaWire Elite, WireClip Torquer Guidewires

FDA Warns of Potentially Serious Problems With Intravascular Device Coatings

Good News, Bad News Week for Watchman LAA Occluder

Quest Medical Voluntarily Recalls Models of Some Blood Pumps Used in Bypass Surgery

Cook Medical Expands Global Recall of Select Sizes of Beacon Tip Angiographic Catheters

Cook Medical Issues Global Recall of Beacon Tip Angiographic Catheter Products

FDA Sounds Alarm Bells Over Use of Lariat Device for LAA Closure in A-fib Patients

CloverSnare™ 4-Loop Vascular Retrieval Snare Recall

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