Abiomed Impella Recall Issued For Heart Pump Catheter’s Instructions Due to Blood Clot Risks
This is the third Impella heart pump recall issued in recent months, following reports of injuries and deaths due to device failures.
This is the third Impella heart pump recall issued in recent months, following reports of injuries and deaths due to device failures.
The FDA has given the Impella heart pump recall a class I designation, meaning the problems could cause severe patient injuries and deaths.
FDA says Abiomed Impella RP Heart Pump Systems are safe enough to use, but must be limited to specific patient populations.