BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HYHSURGPN,400X2D,PBI-AM,-,OQI,5

    MDR report key: 6559511 · Received May 11, 2017

    Report

    Report Number
    2026095-2017-00084
    Event Type
    Malfunction
    Date Received
    May 11, 2017
    Date of Event
    April 3, 2017
    Report Date
    May 25, 2017
    Manufacturer
    HALYARD - IRVINE
    Product Code
    MEB
    UDI-DI
    30680651136238
    PMA / PMN Number
    K063530
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACTUAL DEVICE WAS REPORTED TO BE AVAILABLE BUT HAS NOT YET BEEN RETURNED. THE DEVICE HISTORY RECORD FOR THE REPORTED LOT NUMBER WAS REVIEWED AND DOCUMENTED THAT THE LOT WAS MANUFACTURED ACCORDING TO THE APPROVED MANUFACTURING PROCEDURES, SPECIFICATIONS, AND THEN RELEASED BY QUALITY ASSURANCE. ALL INFORMATION REASONABLY KNOWN AS OF 06-MAY-2017 HAS BEEN INCLUDED IN THIS HEALTH AUTHORITY REPORT. SHOULD ADDITIONAL INFORMATION BE OBTAINED, A FOLLOW-UP HEALTH AUTHORITY REPORT WILL BE PROVIDED. THE INFORMATION PROVIDED BY HALYARD HEALTH REPRESENTS ALL OF THE KNOWN INFORMATION AT THIS TIME. DESPITE GOOD FAITH EFFORTS TO OBTAIN ADDITIONAL INFORMATION, THE COMPLAINANT / REPORTER WAS UNABLE OR UNWILLING TO PROVIDE ANY FURTHER PATIENT, PRODUCT, OR PROCEDURAL DETAILS TO HALYARD HEALTH. HALYARD HEALTH HAS NO INDEPENDENT KNOWLEDGE OF THE EVENT REPORTED BUT IS RELAYING THE INFORMATION THAT WAS PROVIDED BY THE USER FACILITY WHERE THE INCIDENT OCCURRED. THIS PRODUCT INCIDENT IS DOCUMENTED IN THE HALYARD HEALTH COMPLAINT DATABASE AND IDENTIFIED AS COMPLAINT (B)(4). THIS INFORMATION IS SUBMITTED PURSUANT TO 21CFR803, IN COMPLIANCE WITH THE MEDICAL DEVICE REPORTING REQUIREMENT AND SHOULD NOT BE CONSIDERED TO BE AN ADMISSION THAT A HALYARD HEALTH PRODUCT IS DEFECTIVE OR CAUSED SERIOUS INJURY.

    Additional Manufacturer Narrative · 1

    ALL INFORMATION REASONABLY KNOWN AS OF 25-MAY-2017 HAS BEEN INCLUDED IN THIS HEALTH AUTHORITY REPORT. SHOULD ADDITIONAL INFORMATION BE OBTAINED, A FOLLOW-UP HEALTH AUTHORITY REPORT WILL BE PROVIDED. THE INFORMATION PROVIDED BY HALYARD HEALTH REPRESENTS ALL OF THE KNOWN INFORMATION AT THIS TIME. DESPITE GOOD FAITH EFFORTS TO OBTAIN ADDITIONAL INFORMATION, THE COMPLAINANT / REPORTER WAS UNABLE OR UNWILLING TO PROVIDE ANY FURTHER PATIENT, PRODUCT, OR PROCEDURAL DETAILS TO HALYARD HEALTH. HALYARD HEALTH HAS NO INDEPENDENT KNOWLEDGE OF THE EVENT REPORTED BUT IS RELAYING THE INFORMATION THAT WAS PROVIDED BY THE USER FACILITY WHERE THE INCIDENT OCCURRED. (B)(4).

    Additional Manufacturer Narrative · 1

    THE PUMP WAS RETURNED WITH TWO SILVER-SOAKER CATHETERS. PER THE COMPLAINT DESCRIPTION, ONE SILVER-SOAKER CATHETER HAD A TEAR AND THE OTHER HAD NO ISSUES. THE DAMAGED SILVER-SOAKER WAS EXAMINED UNDER A MICROSCOPE AND OBSERVED A TEAR AT THE INFUSION SEGMENT MAGNIFIED AT 3.2X. THE INVESTIGATION SUMMARY CONCLUDED THAT A TEAR WAS OBSERVED AT THE INFUSION SEGMENT OF THE SILVER-SOAKER CATHETER. ALL INFORMATION REASONABLY KNOWN AS OF 22-JUN-2017 HAS BEEN INCLUDED IN THIS HEALTH AUTHORITY REPORT. SHOULD ADDITIONAL INFORMATION BE OBTAINED, A FOLLOW-UP HEALTH AUTHORITY REPORT WILL BE PROVIDED. THE INFORMATION PROVIDED BY HALYARD HEALTH REPRESENTS ALL OF THE KNOWN INFORMATION AT THIS TIME. DESPITE GOOD FAITH EFFORTS TO OBTAIN ADDITIONAL INFORMATION, THE COMPLAINANT / REPORTER WAS UNABLE OR UNWILLING TO PROVIDE ANY FURTHER PATIENT, PRODUCT, OR PROCEDURAL DETAILS TO HALYARD HEALTH. HALYARD HEALTH HAS NO INDEPENDENT KNOWLEDGE OF THE EVENT REPORTED BUT IS RELAYING THE INFORMATION THAT WAS PROVIDED BY THE USER FACILITY WHERE THE INCIDENT OCCURRED. THIS PRODUCT INCIDENT IS DOCUMENTED IN THE HALYARD HEALTH COMPLAINT DATABASE AND IDENTIFIED AS COMPLAINT (B)(4).

    Description of Event or Problem · 1

    HALYARD RECEIVED A SINGLE REPORT THAT REFERENCED TWO DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING ONE PATIENT. THIS IS THE FIRST OF TWO REPORTS. REFER TO 2026095-2017-00085 FOR THE SECOND EVENT. FILL VOLUME: 400. FLOW RATE: 4ML/HR (2+2ML/HR). PROCEDURE:    LAPAROTOMY FOR SMALL BOWEL RESECTION. CATHPLACE:    PRE-PERITONEAL SPACE. A REPORT WAS RECEIVED FROM (B)(4) STATING THE CATHETER SNAPPED FOLLOWING A DIFFICULT REMOVAL. AFTER THE CATHETER WAS SUCCESSFULLY REMOVED IN ITS ENTIRETY, THERE WAS AN APPARENT TEAR TO THE CATHETER, WHICH IS LIKELY THE CAUSE OF THE DIFFICULT REMOVAL. ADDITIONAL INFORMATION RECEIVED 19-APR-2017 STATED THE CATHETER WAS SECURED WITH A SINGLE SUTURE. THE RESISTANCE LEVEL WAS RATED AT 5 ON CATHETER REMOVAL RESISTANCE RATING FROM 0 TO 5. THE CATHETER APPEARED TO BE STRETCHED. DURING REMOVAL, NO PART OF THE CATHETER APPEARED TO BE GRAYISH WHITE. ADDITIONAL INFORMATION RECEIVED 26-APR-2017 STATING THE PAIN BUSTER WAS INSERTED ON (B)(6) 2017 AND REMOVED (B)(6) 2017. THE INSERTION OF THE PAIN BUSTERS WENT IN WITHOUT ANY COMPLICATIONS. THE DEVICES WERE INSERTED INTO THE PRE-PERITONEAL SPACE WITH THE GUIDE NEEDLE AFTER REMOVING THE PLASTIC SHEATH. THE CATHETER WAS THEN INSERTED, DURING THE INSERTION RESISTANCE WAS MET AND THE INSERTION WAS STOPPED. THE CLINICIANS REMOVED THE PLASTIC LINING AND INSERTED SOME LOCAL ANESTHETIC. THIS WENT IN WITH EASE AND THERE WAS NO EVIDENCE OF A BLOCKED CATHETER OR LEAKAGE OF LOCAL ANAESTHETIC ONCE ALL THE ATTACHMENTS WERE MADE. THE DRESSINGS WERE DRY. THE PAIN-BUSTERS WERE NOT ENCOUNTERED DURING THE CLOSURE OF THE MIDLINE LAPAROTOMY WOUND. THE PATIENT DENIED ANY ABDOMINAL PAIN POST OPERATIVELY OR IN RECOVERY AREA.

    Description of Event or Problem · 1

    ADDITIONAL INFORMATION RECEIVED 28-APR-2017 STATED PAIN NURSE PRACTITIONER PROVIDED CLARIFICATION STATING, "THE ACTUAL TEAR OR SPLIT IN THE CATHETER WAS IDENTIFIED ON THE (B)(6) 2017 WHEN IT WAS REMOVED."

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    341664 HYHSURGPN,400X2D,PBI-AM,-,OQI,5 CATHETERS MEB HALYARD - IRVINE PS12508-A 0202415064 30680651136238

    Patients

    Seq Age Sex Outcome Treatment
    1 67 YR