MAUDE Adverse Event Report: TERUMO BCT TRIMA ACCEL; TRIMA ACCEL AUTOMATED BLOOD COLLECTION SYSTEM

Model Number	3810002
Medical Device Problem Codes	Device Slipped (1584); Insufficient Device Problem Information (3190)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	05/28/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Investigation: a terumo bct service technician checked out the device at the customer site.The technician found that the pin on the plastic body panel was engaging the iv pole lever when the button was fully decompressed.The technician adjusted the pin, tested the iv pole, and found no other issues.Investigation is still in process and a follow up report will be provided.
Event or Problem Description
The customer reported that the iv pole on the trima accel equipment unexpectedly lowers down.The iv pole clamp was installed at the time of this event.No adverse event occurred, and no medical intervention was required.No patient (donor) was connected at the time of the event, therefore, no patient information is available.
Additional Manufacturer Narrative
This report is being filed to provide additional information in h.6 and h.11.Investigation: a terumo bct service technician checked out the device at the customer site.The technician found that the pin on the plastic body panel was engaging the iv pole lever when the button was fully decompressed.The technician adjusted the pin, tested the iv pole, and found no other issues.The device serial number history report indicates no further related issues have been reported for this device.Correction: a field service engineer adjusted the iv pole release button.Investigation is still in process and a follow up report will be provided.
Event or Problem Description
The customer reported that the iv pole on the trima accel equipment unexpectedly lowers down.The iv pole clamp was installed at the time of this event.No adverse event occurred, and no medical intervention was required.No patient (donor) was connected at the time of the event, therefore, no patient information is available.
Event or Problem Description
The customer reported that the iv pole on the trima accel equipment unexpectedly lowers down.The iv pole clamp was installed at the time of this event.No adverse event occurred, and no medical intervention was required.No patient (donor) was connected at the time of the event therefore, no patient information is available.
Additional Manufacturer Narrative
This report is being filed to provide additional information in h.6 and h.11.Investigation: a terumo bct service technician checked out the device at the customer site.The technician found that the pin on the plastic body panel was engaging the iv pole lever when the button was fully decompressed.The technician adjusted the pin, tested the iv pole, and found no other issues.The device serial number history report indicates no further related issues have been reported for this device.Correction: a field service engineer adjusted the iv pole release button.Root cause: a root cause assessment was performed for this complaint.The root cause was determined to be related to the need for an iv pole release button adjustment.

• Brand Name: TRIMA ACCEL
• Common Device Name: TRIMA ACCEL AUTOMATED BLOOD COLLECTION SYSTEM
• Manufacturer (Section D): TERUMO BCT; lakewood CO 80215
• Manufacturer (Section G): TERUMO BCT; 10810 w. collins ave; lakewood CO 80215
• Manufacturer Contact: scot hilden ; 10810 w. collins ave; lakewood, CO 80215
• MDR Report Key: 19575804
• Report Number: 1722028-2024-00268
• Device Sequence Number: 12864408
• Product Code: GKT
• UDI-Device Identifier: 05020583810006
• UDI-Public: 05020583810006
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: BK190332
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Administrator/Supervisor
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 06/20/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: 3810002
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/28/2024
• Supplement Date Received by Manufacturer: 07/11/2024; 07/22/2024
• Initial Report FDA Received Date: 06/20/2024
• Supplement Report FDA Received Date: 07/15/2024; 07/23/2024
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 06/21/2022
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown