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HEARTMATE II LVAS IMPLANT KIT (WITH SEALED GRAFTS) Adverse Event — Injury (MDR 2916596-2020-02116)

HEARTMATE II LVAS IMPLANT KIT (WITH SEALED GRAFTS) Adverse Event — Injury (MDR 2916596-2020-02116) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: HEARTMATE II LVAS IMPLANT KIT (WITH SEALED GRAFTS); Generic name: VENTRICULAR (ASSISST) BYPASS; Manufacturer: THORATEC CORPORATION.

DeviceHEARTMATE II LVAS IMPLANT KIT (WITH SEALED GRAFTS)
Generic nameVENTRICULAR (ASSISST) BYPASS
ManufacturerTHORATEC CORPORATION
Report number2916596-2020-02116
Event typeInjury
Product problemN
Date received2020-04-28
Report sourceHEALTH PROFESSIONAL
NarrativeNO FURTHER INFORMATION WAS PROVIDED. A SUPPLEMENTAL REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER¿S INVESTIGATION IS COMPLETED.
SourceopenFDA MAUDE (device adverse events)

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