PERFUSION REPORTS

Perfusion Reports are taken from the Safety Committee web based reporting system and after appropriate anonymising disseminated to the membership. The content should be informative and hopefully encourage similar sharing from the perfusion community. Select any of the options below to go to a dedicated perfusion reports page.

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REPORT NO
070
DATE
Jan 2021
Accidental cardioplegia administration
REPORT NO
069
DATE
June 2021
Sampling manifold valve fault
REPORT NO
068
DATE
May 2021
Human factors issue
REPORT NO
067
DATE
June 2021
Centrimag battery module failure
REPORT NO
066
DATE
April 2021
S5 Double Roller Pump incident
REPORT NO
065
DATE
May 2021
IABP transport issue
REPORT NO
064
DATE
April 2021
Modified Ultrafiltration (MUF) Issue
REPORT NO
063
DATE
March 2021
Electromagnetic interference with HLM
REPORT NO
062
DATE
Feb 2021
HCU40 Failure
REPORT NO
061
DATE
Feb 2021
HCU40 valve failures
REPORT NO
060
DATE
Jan 2021
HCU40 failure
REPORT NO
059
DATE
Jan 2021
LIVA NOVA STATEMENT ON CENTRIFUGAL HEAD

FIELD SAFETY NOTICES (FSN)

A ‘field safety notice’ (FSN) is an important communication about the safety of a medical device that is sent to customers by a device manufacturer, or their representative. FSNs tell you what you need to do to reduce the specified risks of using the medical device. The actions are referred to as ‘field safety corrective actions’ (FSCAs). If you receive a field safety notice from a manufacturer, always act on it.
Select any of the options below to go to a dedicated FSN page.

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London Core Review Cardiothoracic Surgery Course - Help Guide
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REPORT NO
036
DATE
Feb 2021
FSN Medtronic Pixie
REPORT NO
035
DATE
Feb 2021
Getinge IABP Battery Usage, Charging, Storage
REPORT NO
034
DATE
Feb 2021
Getinge HCU40 Replacement of Vacuum Valves
REPORT NO
033
DATE
Dec 2020
Getinge Paediatric Hardshell Reservoir
REPORT NO
032
DATE
Nov 2020
Getinge HLS FSN
REPORT NO
031
DATE
Oct 2020
Getinge HCU40 cable connection FSN
REPORT NO
030
DATE
Sept 2020
Getinge BMU40 FSN
REPORT NO
029
DATE
Aug 2020
Getinge Device Recall IAB
REPORT NO
028
DATE
Aug 2020
Getinge HCU40 Replacment of Vacuum Valves
REPORT NO
027
DATE
July 2020
Getinge Replacement IFU's for HU35 and rotaflow console
REPORT NO
026
DATE
July 2020
Liva Nova Perceval Valve Accessory kit
REPORT NO
025
DATE
July 2020
Medtronic HeartWare HVAD system lubricant