MAUDE Adverse Event Report: B. BRAUN MELSUNGEN AG B. BRAUN; ACCESSORIES, PUMP, INFUSION

Catalog Number	8713112D
Medical Device Problem Code	Thermal Decomposition of Device (1071)
Health Effect - Clinical Code	No Patient Involvement (2645)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Exemption number e2016018 b.Braun inc.(bbmi) (importer) is submitting the report on behalf of b.Braun melsungen ag (manufacturer).This report has been identified as b.Braun medical inc.Internal report number (b)(4).The investigation into this reported event is ongoing.Additional attempts to receive the device involved in the reported incident are being made.A follow-up report will be submitted when the results of the investigation are available.
Event or Problem Description
As reported by user facility: burnt hot prong.
Additional Manufacturer Narrative
Exemption number e2016018 b.Braun inc.(bbmi) (importer) is submitting the report on behalf of b.Braun melsungen ag (manufacturer).This report has been identified as b.Braun medical inc.Internal report number (b)(4) the used power supply was received for evaluation.During the initial visual examination the reported thermal damage was confirmed.Upon further evaluation, it was determined that the pins on the primary adaptor were damaged in a way that caused them to lose connection with the board inside the power supply.The loose connection between the pins and the internal board of the power supply caused the thermal damage.Based on the condition of the power supply when it was received, the cause of the disconnection between the pins and the board was most likely the result of the power supply being dropped several times.If additional information becomes available, a follow up report will be submitted.

• Brand Name: B. BRAUN
• Common Device Name: ACCESSORIES, PUMP, INFUSION
• Manufacturer (Section D): B. BRAUN MELSUNGEN AG; carl-braun-str. 1; melsungen, hessen 34212 ; GM 34212
• MDR Report Key: 8335744
• Report Number: 9610825-2019-00009
• Device Sequence Number: 1663151
• Product Code: MRZ
• UDI-Device Identifier: 04046964085673
• UDI-Public: (01)04046964085673
• Combination Product (Y/N): N
• Initial Reporter State: CA
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional,user faci
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 03/29/2019
• Report Date (Section F): 03/29/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Catalogue Number: 8713112D
• Was Device Available for Evaluation?: Yes
• Was the Report Sent to FDA?: Yes
• Distributor Facility Aware Date: 01/21/2019
• Device Age: 4 YR
• Event Location: Hospital
• Date Report to Manufacturer: 03/29/2019
• Initial Date Received by Manufacturer: 01/21/2019
• Supplement Date Received by Manufacturer: 01/21/2019
• Initial Report FDA Received Date: 02/13/2019
• Supplement Report FDA Received Date: 03/29/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Date Report Sent to FDA: 03/29/2019