MAUDE Adverse Event Report: TERUMO BCT TRIMA ACCEL; TRIMA ACCEL PLATELET SAMPLER PLASMA AUTO RBC SET(ISBT)

Catalog Number	80360
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	No Patient Involvement (2645)
Date of Event	05/20/2019
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Investigations: the device history records (dhr) were reviewed for this lot.There were no events noted in the dhr that would have contributed to the elevated wbc count experienced by the customer.Investigation is in process, a follow-up report will be provided.
Event or Problem Description
The customer would like the run data file investigated to determine a possible cause for the elevated white blood cell (wbc) content in the red blood cell (rbc) product.There was not a transfusion recipient or patient involved at the time of the residual white blood cell (rwbc) testing, therefore no patient information is reasonably known at the time of the event.The platelet collection set is not available for return because it was discarded by the customer.
Additional Manufacturer Narrative
This report is being filed to provide in investigation: the run data file (rdf) was analyzed for this event.Root cause: the analysis of the run data file did not find a conclusive cause for the higher-than-expected wbc content reported in the rbc product for this collection.No unusual processvariable was identified and the signals in the run data file indicate that the trima accel systemoperated as intended.Based on the available information, it is possible that the filter was unloadedfrom the filter bracket and loaded again during rbc collection or rbc additive solution addition,which could have a similar affect to ¿squeezing¿ the filter when using a gravity drain system.It isalso possible that the reported results could be attributed to an issue with the filter or donorrelated.

• Brand Name: TRIMA ACCEL
• Common Device Name: TRIMA ACCEL PLATELET SAMPLER PLASMA AUTO RBC SET(ISBT)
• Manufacturer (Section D): TERUMO BCT; lakewood CO 80215
• MDR Report Key: 8744753
• Report Number: 1722028-2019-00160
• Device Sequence Number: 2043445
• Product Code: GKT
• UDI-Device Identifier: 05020583803602
• UDI-Public: 05020583803602
• Combination Product (Y/N): N
• Initial Reporter State: VA
• Initial Reporter Country: US
• PMA/510(K) Number: BK180231
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 06/28/2019

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 Expiration Date: 03/01/2021
• Device Catalogue Number: 80360
• Device Lot Number: 1903282230
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/04/2019
• Supplement Date Received by Manufacturer: 07/03/2019
• Initial Report FDA Received Date: 06/28/2019
• Supplement Report FDA Received Date: 07/09/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other