MedPage Today on MSN1d
Tack System Recall; Gene Hackman's Pacemaker; Altitude and Valve Disease?
The FDA said to stop all use of Philips' Tack Endovascular System, which is under class I recall for user difficulties in ...
Modern Healthcare1d
FDA labels Philips' recall of Tack Endovascular Systems a Class I
Complications with the implant used to treat blood vessel dissection after balloon angioplasty or stent placement can result ...
MassDevice2d
Philips discontinues Tack endovascular system sales after serious recall
This recall involves removing devices from use and sale. According to the FDA notice, the device may cause serious injury of ...
Endovascular Today4h
Philips Recalls, Removes, and Discontinues Distribution of Tack Endovascular System
The FDA advised this week that Philips is recalling the Tack endovascular systems because of challenges experienced by customers d ...
GlobalData on MSN2d
Philips pulls endovascular implant from market after FDA Class I recall tag
Philips has recommended that customers immediately stop using affected Tack endovascular systems and return unused product to ...
TCTMD2d
Philips Recalls Tack Endovascular Systems and Stops Distribution
The FDA says user challenges and need for additional procedures drove recommendations to stop using the system immediately.
MedTech Dive1d
Philips pulls endovascular implant from market after 20 injuries
Philips stopped selling its Tack endovascular system because of cases where additional interventions were needed to remove ...
Fierce Biotech2d
FDA elevates endovascular recall as Philips pulls Tack implant from the market
Philips is pulling from the market an implant designed to help repair the interior of damaged blood vessels, following a serious product recall. | Philips is pulling from the market an implant ...
FDA says Philips to discontinue distribution of Tack Endovascular System
The U.S. Food & Drug Administration said that Philips has removed and discontinued distribution of Tack Endovascular System ...
BioWorld2d
Philips pulls Tack device due to problems with deployment
Royal Phillips NV opted to withdraw the Tack endovascular repair device only six years after the U.S. FDA’s approved it. Tack is designed to repair vascular dissection caused by angioplasty. The ...