MAUDE Adverse Event Report: CONCORD MANUFACTURING 2008T HEMODIALYSIS SYSTEM WITHOUT CDX; DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM

Model Number	190858
Medical Device Problem Code	Thermal Decomposition of Device (1071)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/11/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Plant investigation: the plant investigation is in process.A supplemental mdr will be submitted upon completion of this activity.
Event or Problem Description
A user facility biomedical technician (bmt) reported that a fresenius 2008t hemodialysis (hd) machine was experiencing low conductivity.The bmt stated he noticed the cable on the acid pump was burned.The bmt was issued a replacement acid pump.It is unknown if the acid cable was available to be returned for manufacturer evaluation.There was no patient involvement associated with the reported event.Additional information was requested, however to date has not been provided.
Additional Manufacturer Narrative
Plant investigation: no parts were returned to the manufacturer for physical evaluation.Additionally, no on-site evaluation was performed by a fresenius field service technician (fst).A records review was performed on the reported serial number.An investigation of the device manufacturing records was conducted by the manufacturer.There were no non-conformances, or any associated rework identified during the manufacturing process which could be related to the reported event.In addition, the device history record (dhr) review confirmed the results of the in-progress and final quality control (qc) testing met all requirements.The investigation into the cause of the reported problem was not able to be confirmed.A definitive conclusion regarding the complaint incident cannot be reached without a physical examination of the complaint device.
Event or Problem Description
A user facility biomedical technician (bmt) reported that a fresenius 2008t hemodialysis (hd) machine was experiencing low conductivity.The bmt stated he noticed the cable on the acid pump was burned.The bmt was issued a replacement acid pump.It is unknown if the acid cable was available to be returned for manufacturer evaluation.There was no patient involvement associated with the reported event.Additional information was requested, however to date has not been provided.
Event or Problem Description
A user facility biomedical technician (bmt) reported that a fresenius 2008t hemodialysis (hd) machine was experiencing low conductivity.The bmt stated he noticed the cable on the acid pump was burned.The bmt was issued a replacement acid pump.It is unknown if the acid cable was available to be returned for manufacturer evaluation.There was no patient involvement associated with the reported event.Additional information was requested, however to date has not been provided.
Additional Manufacturer Narrative
Correction: g2.

• Brand Name: 2008T HEMODIALYSIS SYSTEM WITHOUT CDX
• Common Device Name: DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM
• Manufacturer (Section D): CONCORD MANUFACTURING; director, quality systems; 4040 nelson avenue; concord CA 94520
• MDR Report Key: 12053256
• Report Number: 2937457-2021-01308
• Device Sequence Number: 14318833
• Product Code: KDI
• UDI-Device Identifier: 00840861100903
• UDI-Public: 00840861100903
• Combination Product (Y/N): N
• Initial Reporter State: NJ
• Initial Reporter Country: US
• PMA/510(K) Number: K113427
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: consumer,health professional
• Initial Reporter Occupation: Biomedical Engineer
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 07/12/2021

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: 190858
• Device Catalogue Number: 190858
• Was Device Available for Evaluation?: No
• Device Age: MO
• Initial Date Received by Manufacturer: 06/11/2021
• Supplement Date Received by Manufacturer: 07/07/2021; 07/09/2021
• Initial Report FDA Received Date: 06/23/2021
• Supplement Report FDA Received Date: 07/08/2021; 07/12/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1