Modern Healthcare14h
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 ...
Hosted on MSN1d
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 ...
medtechdive17h
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 ...
MassDevice1d
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 ...
Hosted on MSN1d
Tack System Recall; Gene Hackman's Pacemaker; Altitude and Valve Disease?
Data from two French registries suggested that the need for reintervention after transcatheter aortic valve replacement was ...
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 ...
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.
FierceBiotech1d
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 ...