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Model Number 673662 |
Device Problem
Occlusion Within Device (1423)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 04/24/2017 |
Event Type
malfunction
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Manufacturer Narrative
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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.A good faith effort will be made to obtain the applicable information relevant to the report.If information is provided in the future, a supplemental report will be issued.
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Event Description
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According to the reporter, the unit presented a blockage in the administration line after 6 hours of use.No sample will be returned for evaluation.There are no companion samples to be returned.There was patient involvement and no patient injury, medical intervention, or adverse reaction associated with this event.No further information required is available.
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Search Alerts/Recalls
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