The complainant indicated that the device will not be returned for evaluation; therefore, a failure analysis is not available, and we are not able to determine the relationship between this device and the cause for this event. as part of our manufacturing process, all device history records are reviewed and approved by quality, prior to release of product. if additional information or the sample is received, the investigation will be reopened and responded to accordingly.
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The customer reported that spike set presented a nutrition leakage in the spike connection.The event was occurred during priming.There was no patient involved, no patient injury, medical intervention, or adverse reaction is associated with this event.
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