Model Number 81000 |
Device Problems
Mechanical Problem (1384); Device Slipped (1584)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 05/17/2022 |
Event Type
malfunction
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Manufacturer Narrative
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Investigation: the terumo bct technician was able to duplicate the issue on the device at the customer site.The iv pole bracket was adjusted to proper operation and returned to service.Investigation is in process.A follow up report will be provided.
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Event Description
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The customer reported that the iv pole keeps falling down.There was not a patient involved at the time of the iv pole falling, therefore patient information is not reasonably known.
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Manufacturer Narrative
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This report is being filed to provide additional information in h.6 and h.10.Investigation: the terumo bct technician was able to duplicate the issue on the device at the customer site.The iv pole bracket was adjusted to proper operation and returned to service.The device serial number history report indicates no further related issues have been reported for this device.Investigation is in process.A follow up report will be provided.
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Event Description
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The customer reported that the iv pole keeps falling down.There was not a patient involved at the time of the iv pole falling, therefore patient information is not reasonably known.
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Event Description
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The customer reported that the iv pole keeps falling down.There was not a patient involved at the time of the iv pole falling, therefore patient information is not reasonably known.
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Manufacturer Narrative
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Investigation: the terumo bct technician was able to duplicate the issue on the device at the customer site.The iv pole bracket was adjusted to proper operation and returned to service.Service confirmed that all trima devices at the customer site have iv pole safety collars installed.No injuries were reported.The device serial number history report indicates no further related issues have been reported for this device.One year of service history was reviewed for this device with no issues related to the reported condition identified.Root cause: a root cause assessment was performed for this complaint.The root cause was determined to be related to an iv pole adjustment screw that needed positioned for proper stability.
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Search Alerts/Recalls
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