Concerns raised7
Failure to align product promotion with safety information about feeding and drainage suitability
Insufficient product description of the tube bore restriction
Failure to fully evaluate the size 14FR tube before replacing previous drainage tubes
Lack of compulsory root cause analysis training for clinicians
Failure to train sales marketing staff to recognise and communicate the tube bore restriction
Failure to respond appropriately when NG tubes are not adequately draining
Wider product labelling failure to communicate the connector-related bore restriction
No linked response statementsNo action or position from this recipient is clearly linked to the concerns in this report.
Concerns raised8
Lack of compulsory root cause analysis training for clinicians
Inadequate evaluation and feedback before wholesale replacement of drainage tubes
Continued promotion of the product as suitable for feeding and drainage despite safety information
Wider product labelling problem regarding the tube's restricted bore
Failure to train sales marketing staff to recognise and communicate the tube's restricted bore
Insufficient product description of the tube's restricted bore
Lack of recognition of the need to aspirate the tube
Failure to consider alternative action when nasogastric tubes do not adequately drain
No linked response statementsNo action or position from this recipient is clearly linked to the concerns in this report.