Model Number PRI TUBING |
Device Problem
False Alarm (1013)
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Patient Problems
No Consequences Or Impact To Patient (2199); No Information (3190)
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Event Type
malfunction
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Manufacturer Narrative
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Although requested, product has not been received.A follow up report will be submitted with failure investigation results should the product be received for evaluation.Customer states 15 occurrences in the last 2 months.
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Event Description
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It was reported that (b)(6) rn, reported experiencing air-in-line alarms with no visible air noted in the tubing with maintenance iv fluids.She stated she changed the iv pump channel and continued to experience air-in-line alarms.She had to change the iv set to get resolution of the air-in-line alarms.She stated this has happened to her approximately 15 times in the last 2 months.No additional information was available.
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Event Description
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It was reported that (b)(6), rn, reported experiencing air-in-line alarms with no visible air noted in the tubing with maintenance iv fluids.She stated she changed the iv pump channel and continued to experience air-in-line alarms.She had to change the iv set to get resolution of the air-in-line alarms.She stated this has happened to her approximately 15 times in the last 2 months.There was no patient harm.No additional information was available.
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Event Description
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It was reported that erin murray, rn, reported experiencing air-in-line alarms with no visible air noted in the tubing with maintenance iv fluids.She stated she changed the iv pump channel and continued to experience air-in-line alarms.She had to change the iv set to get resolution of the air-in-line alarms.She further stated that this has happened to her approximately (15) times in the last (2) months.There was no patient harm.No additional information was available.
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Manufacturer Narrative
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Initially reportable but additional clinical review determined this to be not reportable.- supplemental mdr created to report non-reportability.
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Search Alerts/Recalls
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