BEUDAMED
    FDA Adverse Event Injury Summary report: N

    I DON'T KNOW I AM NOT A DOCTOR

    MDR report key: 2479649 · Received February 29, 2012

    Report

    Report Number
    MW5024503
    Event Type
    Injury
    Date Received
    February 29, 2012
    Date of Event
    December 27, 2005
    Report Date
    February 29, 2012
    Manufacturer
    UNK
    Product Code
    HDB
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    SON WAS SUBJECTED TO HOURS OF INADEQUATE OXYGEN, ONLY ONE DOCTOR ON DUTY, NURSE FAILED TO DO ANYTHING, DOCTOR EVENTUALLY CAME IN, USED VACUUM MACHINE AND PULLED HIM WITH FORCE AFTER ONE PUSH. SON HAD HORRIFIC BLOOD CORD GASSES, HAS HAD SEIZURES SINCE 8 HOURS OF LIFE, DIAGNOSED WITH CEREBRAL PALSY AS A RESULT. THE HOSPITAL TRIED TO SWEEP THE ENTIRE INCIDENT UNDER THE RUG AND I AM ALMOST POSITIVE THAT THEY HAVE NEVER REPORTED THIS INCIDENT. PLEASE FOLLOW UP TO SEE IF THEY HAVE REPORTED THAT THEY USED A VACUUM TO ASSIST IN THE DELIVERY THAT TOOK PLACE AT 5:56 ON THE MORNING OF (B)(6) 2005, I BEG OF YOU, THIS HOSPITAL FAILED THE STANDARD OF...AND DESERVES EVERY POSSIBLE SANCTION FOR THEIR LACK OF INTEGRITY WITHIN THE MEDICAL COMMUNITY. IF THEY DID NOT REPORT THIS ONE, IT MAKES ME WONDER HOW MANY OTHERS THEY HAVE NOT REPORTED THAT HAD SERIOUS INJURIES. MY WIFE STILL TO THIS DAY NEEDS RECONSTRUCTIVE SURGERY BECAUSE OF THE USE OF FORCE WITH THE VACUUM. VACUUM ASSIST WAS ADMINISTERED ON THE MORNING OF (B)(6) 2005 BY DR. (B)(6) WHO IS EMPLOYED BY (B)(6) HOSPITAL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 I DON'T KNOW I AM NOT A DOCTOR VACUUM MACHINE HDB UNK 1111

    Patients

    Seq Age Sex Outcome Treatment
    1 1 DA Life Threatening| R