BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    IVF PASTEUR PIPET PLUGGED

    MDR report key: 11814606 · Received May 12, 2021

    Report

    Report Number
    1216677-2021-00102
    Event Type
    Malfunction
    Date Received
    May 12, 2021
    Date of Event
    January 27, 2021
    Report Date
    February 22, 2021
    Manufacturer
    COOPERSURGICAL, INC.
    Product Code
    MQH
    PMA / PMN Number
    K161275
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    INVESTIGATION: X-NO SAMPLE RETURNED, X-REVIEW DHR. ANALYSIS AND FINDINGS: (B)(4). WAS THE COMPLAINT CONFIRMED? NO. DISTRIBUTION HISTORY: THE COMPLAINT PRODUCT WAS PURCHASED FROM A SUPPLIER (FISHER SCIENTIFIC), PACKAGED BY CSI IN MARCH 2020 UNDER WORK ORDER: (B)(4). MANUFACTURING RECORD REVIEW: DHR 286741 WAS REVIEWED AND NO NON-CONFORMITIES, RELATED TO THE COMPLAINT CONDITION, WERE NOTED. INCOMING INSPECTION REVIEW: A REVIEW OF THE INCOMING INSPECTION RECORD COULD NOT BE PERFORMED AS THE COMPONENT PART: (PP-5.75-FP) IS NOT LOT CONTROLLED. SERVICE HISTORY RECORD: SERVICE HISTORY NOT APPLICABLE FOR THIS PRODUCT. HISTORICAL COMPLAINT REVIEW: A REVIEW OF THE 2-YEAR COMPLAINT HISTORY DID NOT SHOW SIMILAR REPORTED COMPLAINT CONDITIONS. PRODUCT RECEIPT: THE COMPLAINT PRODUCT HAS NOT BEEN RETURNED TO COOPERSURGICAL. VISUAL EVALUATION: EVALUATION OF THE COMPLAINT PRODUCT COULD NOT BE COMPLETED AS THE COMPLAINT PRODUCT HAS NOT BEEN RETURNED TO COOPERSURGICAL. IF THE PRODUCT SHOULD BE RETURNED AT A LATER DATE, IT WILL BE EVALUATED, AND ANY FINDINGS WILL BE APPENDED TO THIS INVESTIGATION. FUNCTIONAL EVALUATION: EVALUATION OF THE COMPLAINT PRODUCT COULD NOT BE COMPLETED AS THE COMPLAINT PRODUCT HAS NOT BEEN RETURNED TO COOPERSURGICAL. IF THE PRODUCT SHOULD BE RETURNED AT A LATER DATE, IT WILL BE EVALUATED, AND ANY FINDINGS WILL BE APPENDED TO THIS INVESTIGATION. ROOT CAUSE: ROOT CAUSE NOT APPLICABLE AS THE COMPLAINT CONDITION WAS NOT CONFIRMED. IT SHOULD BE NOTED THAT THIS WORK ORDER HAD 1-CELL MEA AND ENDOTOXIN TESTS CONDUCTED ON THE PRODUCT AND BOTH TESTS PASSED. CORRECTION AND/OR CORRECTIVE ACTION: NO OTHER COMPLAINTS REPORTED THAT RELATE TO THIS LOT NUMBER. NO FURTHER CORRECTIVE ACTION IS NECESSARY, AS THE COMPLAINT CONDITION WAS NOT CONFIRMED. NO FURTHER TRAINING REQUIRED AT THIS TIME. PREVENTATIVE ACTION ACTIVITY: COOPERSURGICAL WILL CONTINUE TO MONITOR THIS COMPLAINT CONDITION FOR TRENDS.

    Description of Event or Problem · 0

    MULTIPLE REPORTS ON TIPS & PIPETTE SUBMITTED BY CSI UK. INCIDENT DETAIL: THEY HAVE HAD A LAB INFECTION. THIS IS ACROSS MULTIPLE PATIENTS. THEY SUSPECT THAT THE MOST LIKELY SOURCE IS THE GTL MEDIA FROM VL. THIS IS BASED ON ONE OTHER REPORT FROM A CLINIC (B)(6) KNOWS. THEY NEED TO HOWEVER WORK THROUGH A PROCESS OF ELIMINATION AND WILL LIKE TO SEE IF WE HAVE HAD ANY REPORTS ON THE ITEMS LISTED, THEY ARE IN COMMON IN THE INFECTED PATIENTS TREATMENT CYCLES. I DO NOT WANT TO PUT PROCEED WITH A COMPLAINT AS I DO NOT SEE THIS AS A COMPLAINT BUT AN INVESTIGATION, HOWEVER, WILL TAKE DIRECTION FROM YOU AS TO HOW IT MAY BEST TO CAPTURE THE SITUATION AND ALSO THE SPECIFICS OF THE COMMUNICATION TO THE CUSTOMER. CUSTOMER JUST WISHES TO KNOW IF ANY ITEMS FROM THESE LOTS HAVE ALSO BEEN INVESTIGATED FOR INFECTION - NO ACTUAL COMPLAINT HERE. CUSTOMER CONTACT: (B)(6). 1216677-2021-00102 IVF PASTEUR PIPET PLUGGED PP 5-75-1000PL (B)(4).

    Additional Manufacturer Narrative · 1

    COOPERSURGICAL, INC. IS CURRENTLY INVESTIGATING THE CONDITION REPORTED.

    Description of Event or Problem · 1

    MULTIPLE REPORTS ON TIPS & PIPETTE SUBMITTED BY CSI (B)(4). INCIDENT DETAIL- THEY HAVE HAD A LAB INFECTION. THIS IS ACROSS MULTIPLE PATIENTS. THEY SUSPECT THAT THE MOST LIKELY SOURCE IS THE GTL MEDIA FROM VL. THIS IS BASED ON ONE OTHER REPORT FROM A CLINIC (B)(6) KNOWS. THEY NEED TO HOWEVER WORK THROUGH A PROCESS OF ELIMINATION AND WILL LIKE TO SEE IF WE HAVE HAD ANY REPORTS ON THE ITEMS LISTED, THEY ARE IN COMMON IN THE INFECTED PATIENTS TREATMENT CYCLES. I DO NOT WANT TO PUT PROCEED WITH A COMPLAINT AS I DO NOT SEE THIS AS A COMPLAINT BUT AN INVESTIGATION, HOWEVER, WILL TAKE DIRECTION FROM YOU AS TO HOW IT MAY BEST TO CAPTURE THE SITUATION AND ALSO THE SPECIFICS OF THE COMMUNICATION TO THE CUSTOMER. CUSTOMER JUST WISHES TO KNOW IF ANY ITEMS FROM THESE LOTS HAVE ALSO BEEN INVESTIGATED FOR INFECTION - NO ACTUAL COMPLAINT HERE. CUSTOMER CONTACT- (B)(6). IVF PASTEUR PIPET PLUGGED PP 5-75-1000PL. E-COMPLAINT- (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    712203 IVF PASTEUR PIPET PLUGGED IVF PASTEUR PIPET PLUGGED MQH COOPERSURGICAL, INC. PP-5.75-1000PL 286471

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown Other