MAUDE Adverse Event Report: ERIKA DE REYNOSA, S.A. DE C.V. CUSTOM COMBI SET; SET, TUBING, BLOOD, WITH AND WITHOUT ANTI-REGURGITATION VALVE

Catalog Number	03-2742-9
Medical Device Problem Code	Fluid/Blood Leak (1250)
Health Effect - Clinical Code	Hemorrhage/Blood Loss/Bleeding (1888)
Date of Event	09/07/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The plant investigation is in process.A supplemental mdr will be submitted upon completion of this activity. .
Event or Problem Description
A user facility¿s program manager reported that a customer combi set disconnected 20 seconds into a patient¿s hemodialysis (hd) treatment.The disconnection occurred at the ¿t¿ connection.The machine, a fresenius 2008t hemodialysis machine, did not alarm, but was not expected to.A fresenius dialyzer was also in use.The patient¿s estimated blood loss (ebl) was approximately 20ml.There was no patient injury, adverse event or medical intervention required as a result of this event.The patient was restarted on the same machine and treatment completed successfully with new supplies.The complaint device discarded, but a photo has been provided.
Event or Problem Description
A user facility¿s program manager reported that a customer combi set disconnected 20 seconds into a patient¿s hemodialysis (hd) treatment.The disconnection occurred at the ¿t¿ connection.The machine, a fresenius 2008t hemodialysis machine, did not alarm, but was not expected to.A fresenius dialyzer was also in use.The patient¿s estimated blood loss (ebl) was approximately 20ml.There was no patient injury, adverse event or medical intervention required as a result of this event.The patient was restarted on the same machine and treatment completed successfully with new supplies.The complaint device discarded, but a photo has been provided.
Additional Manufacturer Narrative
Plant investigation: as the device was not returned to the manufacturer, a physical evaluation could not be performed.However, a photograph of the combi set connected to the machine was provided by the customer.According to the photo received, a separation was observed from the arterial line to the ¿t¿ saline connector.The condition of the tubing and connector could not be observed.The alleged failure mode was confirmed; a separation was observed according to the photo received from the customer.This kind of failure could be caused due to an incorrect solvent application on the component or due to a lack of solvent during the assembly of the components.A batch records review was conducted by the manufacturer for the reported lot.There were no non-conformances or abnormalities identified during the manufacturing process which could be associated with the reported event.The entire lot has been sold and distributed.In addition, a device history review was performed and confirmed that the results of the in-progress and final quality control (qc) testing met all requirements.The lot met all specifications for release.The reported event was confirmed based on the provided photograph.
Additional Manufacturer Narrative
Corrected information: e1.
Event or Problem Description
A user facility¿s program manager reported that a customer combi set disconnected 20 seconds into a patient¿s hemodialysis (hd) treatment.The disconnection occurred at the ¿t¿ connection.The machine, a fresenius 2008t hemodialysis machine, did not alarm, but was not expected to.A fresenius dialyzer was also in use.The patient¿s estimated blood loss (ebl) was approximately 20ml.There was no patient injury, adverse event or medical intervention required as a result of this event.The patient was restarted on the same machine and treatment completed successfully with new supplies.The complaint device discarded, but a photo has been provided.

• Brand Name: CUSTOM COMBI SET
• Common Device Name: SET, TUBING, BLOOD, WITH AND WITHOUT ANTI-REGURGITATION VALVE
• Manufacturer (Section D): ERIKA DE REYNOSA, S.A. DE C.V.; mike allen #1331; parque industrial reynosa; reynosa 88780 ; MX 88780
• Manufacturer (Section G): ERIKA DE REYNOSA, S.A. DE C.V.; director, quality systems; 900 w zaragosa drive suite d; pharr TX 78577
• Manufacturer Contact: jessica trujillo ; 920 winter st; waltham, MA 02451 ; 6174175172
• MDR Report Key: 20215613
• Report Number: 0008030665-2024-00777
• Device Sequence Number: 7328014
• Product Code: FJK
• UDI-Device Identifier: 00840861100309
• UDI-Public: 00840861100309
• Combination Product (Y/N): N
• Initial Reporter State: NC
• Initial Reporter Country: US
• PMA/510(K) Number: K962081
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility,Company Representative
• Initial Reporter Occupation: Nurse
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 10/14/2024

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 Catalogue Number: 03-2742-9
• Device Lot Number: 24DR01202
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Device Age: MO
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/09/2024
• Supplement Date Received by Manufacturer: 10/09/2024; 10/11/2024
• Initial Report FDA Received Date: 09/13/2024
• Supplement Report FDA Received Date: 10/09/2024; 10/14/2024
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 04/08/2024
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: FRESENIUS DIALYZER.; FRESENIUS DIALYZER.; FRESENIUS DIALYZER.; FRESENIUS HEMODIALYSIS MACHINE.; FRESENIUS HEMODIALYSIS MACHINE.; FRESENIUS HEMODIALYSIS MACHINE.
• Patient Age: 46 YR
• Patient Sex: Male