Medindia9d
Recall of Artificial Heart Devices for Heart Transplant by FDA
The FDA has issued a recall for Abbott's HeartMate 3 artificial heart devices, critical for heart transplant patients, due to ...
MassDevice10d
Hologic’s radiographic marker implant recall is serious due to complications with implanted devices
Hologic recalled the marker due to complications and adverse events reported with implanted devices. The recall is a ...
Yahoo Finance18d
FDA recalls Abbott’s HeartMate 3 ventricular assist device after 2 deaths
which is used to monitor patients who have an implantable HeartMate 3 device. The recall was issued after the FDA identified issues with the seal interface between the LVAD inflow cannula and the ...
FierceBiotech20d
FDA elevates cardiovascular catheter recalls from Boston Scientific, Route 92 Medical
FDA elevates cardiovascular catheter recalls from Boston Scientific, Route 92 Medical By Conor Hale May 14, 2024 12:15pm Boston Scientific Route 92 Medical cardiovascular disease Class I recall ...
FDA classifies recall of Hologic's implant as 'most serious'
The U.S. Food and Drug Administration on Wednesday classified a recall of Hologic's devices that are implanted in soft tissue ...
Becker's Hospital Review25d
48 injuries, deaths tied to Getinge heart devices: FDA
The FDA is instructing healthcare facilities to avoid using two heart devices from Getinge amid concerns that the company has not adequately resolved issues that spurred a string of recalls over ...
Morningstar24d
Getinge Shares Sink After FDA Warns on Heart Devices
In a statement Wednesday, the FDA said it recommended providers find alternatives to Getinge's balloon pump and bypass devices ... to the heart's left ventricle. Eight of the recalls fall within ...
Reuters24d
US FDA advises healthcare facilities to switch from Getinge's heart devices
May 8 (Reuters) - The U.S Food and Drug Administration ... opens new tab heart devices in patients as they faced safety and quality concerns despite a string of recalls. The recommendation ...
WSAY11d
FDA classifies recall of Hologic’s implants for soft tissue as ‘most serious’
The U.S. Food and Drug Administration on Wednesday classified a recall of Hologic's devices that are implanted in soft tissue ...
Yahoo12d
FDA classifies recall of Hologic's implant as 'most serious'
(Reuters) -The U.S. Food and Drug Administration on Wednesday classified a recall of Hologic's devices that are implanted in soft tissue such as breast tissue as "most serious", and urged doctors ...