MAUDE Adverse Event Report: ERIKA DE REYNOSA, S.A. DE C.V. SAFE LOCK APD LUER LOCK CONNECTOR; SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

Model Number	050-95018
Medical Device Problem Code	Fluid/Blood Leak (1250)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	11/27/2021
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
It was reported that a peritoneal dialysis (pd) patient discovered a fluid leak from the apd luer lock connection during dwell 1 of 4 of their pd treatment.There were no alarms associated with the fluid leak.It is unknown at which point in therapy the leak may have begun.The cause of the leak is unknown.The patient was advised to cancel treatment and re-setup the cycler with new supplies.Upon follow up, the patient stated they did not complete treatment on the night of the fluid leak.The patient did not develop any symptoms, adverse events, injuries, or require medical intervention as a result of the reported event.The patient confirmed they are continuing peritoneal dialysis therapy with no further issues.The luer lock connector used by the patient was discarded and is not available for return for physical evaluation by the manufacturer.
Additional Manufacturer Narrative
Plant investigation: as the device was not returned to the manufacturer, a physical evaluation could not be performed.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.A product history review did not reveal a probable cause for the customer complaint.As a physical evaluation could not be performed, a definitive conclusion regarding the reported incident could not be reached and a cause could not be confirmed.
Event or Problem Description
It was reported that a peritoneal dialysis (pd) patient discovered a fluid leak from the apd luer lock connection during dwell 1 of 4 of their pd treatment.There were no alarms associated with the fluid leak.It is unknown at which point in therapy the leak may have begun.The cause of the leak is unknown.The patient was advised to cancel treatment and re-setup the cycler with new supplies.Upon follow up, the patient stated they did not complete treatment on the night of the fluid leak.The patient did not develop any symptoms, adverse events, injuries, or require medical intervention as a result of the reported event.The patient confirmed they are continuing peritoneal dialysis therapy with no further issues.The luer lock connector used by the patient was discarded and is not available for return for physical evaluation by the manufacturer.
Event or Problem Description
It was reported that a peritoneal dialysis (pd) patient discovered a fluid leak from the apd luer lock connection during dwell 1 of 4 of their pd treatment.There were no alarms associated with the fluid leak.It is unknown at which point in therapy the leak may have begun.The cause of the leak is unknown.The patient was advised to cancel treatment and re-setup the cycler with new supplies.Upon follow up, the patient stated they did not complete treatment on the night of the fluid leak.The patient did not develop any symptoms, adverse events, injuries, or require medical intervention as a result of the reported event.The patient confirmed they are continuing peritoneal dialysis therapy with no further issues.The luer lock connector used by the patient was discarded and is not available for return for physical evaluation by the manufacturer.

• Brand Name: SAFE LOCK APD LUER LOCK CONNECTOR
• Common Device Name: SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
• 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; 1100 e, military hwy, suite c; pharr TX 78577
• Manufacturer Contact: jason busch ; 920 winter st; waltham, MA 02451 ; 9043166958
• MDR Report Key: 12893966
• Report Number: 8030665-2021-01789
• Device Sequence Number: 11649567
• Product Code: KDJ
• UDI-Device Identifier: 00840861100811
• UDI-Public: 00840861100811
• Combination Product (Y/N): N
• Initial Reporter State: MI
• Initial Reporter Country: US
• PMA/510(K) Number: K124024
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Consumer
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 12/24/2021

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: Lay User/Patient
• Device Expiration Date: 06/30/2022
• Device Model Number: 050-95018
• Device Catalogue Number: 050-95018
• Device Lot Number: 21HR08084
• Was Device Available for Evaluation?: No
• Device Age: MO
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 11/27/2021
• Supplement Date Received by Manufacturer: 12/09/2021; 12/22/2021
• Initial Report FDA Received Date: 11/30/2021
• Supplement Report FDA Received Date: 12/21/2021; 12/23/2021
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 06/30/2021
• 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: DELFLEX PD FLUID; DELFLEX PD FLUID; DELFLEX PD FLUID; LIBERTY CYCLER SET; LIBERTY CYCLER SET; LIBERTY CYCLER SET; LIBERTY SELECT CYCLER; LIBERTY SELECT CYCLER; LIBERTY SELECT CYCLER
• Patient Age: 67 YR
• Patient Sex: Male
• Patient Weight: 89 KG