Catalog Number 2H7462 |
Device Problem
Device Displays Incorrect Message (2591)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Type
malfunction
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Manufacturer Narrative
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(b)(4).Should additional relevant information become available, a supplemental report will be submitted.
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Event Description
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It was reported that an unspecified number of clearlink secondary sets continually cause ¿upstream occlusion¿ alarms without any obvious cause.These were identified during patient infusions and while in use on a pump; further described as ¿especially when the customer inserts the secondary tubing into the distal y site of the primary tubing¿.There was no report of patient injury or medical intervention associated with these events.No additional information is available.
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Manufacturer Narrative
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The devices were not returned and the lot number is unknown; therefore, a device analysis could not be completed.Should additional relevant information become available, a supplemental report will be submitted.
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Search Alerts/Recalls
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