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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MEDTRONIC POWERED SURGICAL MIDAS REX MRT PNEUMATIC HIGH SPEED SYSTEM; MOTOR, DRILL, PNEUMATIC

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MEDTRONIC POWERED SURGICAL MIDAS REX MRT PNEUMATIC HIGH SPEED SYSTEM; MOTOR, DRILL, PNEUMATIC Back to Search Results
Model Number MEDT T9850/C0375
Device Problems Break (1069); Detachment Of Device Component (1104)
Patient Problem No Information (3190)
Event Date 12/08/2015
Event Type  Injury  
Event Description
Midas rex footplace broke off during the craniotomy for tumor.Midas rex legend #8 is the specific drill involved.
 
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Brand Name
MIDAS REX MRT PNEUMATIC HIGH SPEED SYSTEM
Type of Device
MOTOR, DRILL, PNEUMATIC
Manufacturer (Section D)
MEDTRONIC POWERED SURGICAL
4620 north beach st.
fort worth TX 76137
MDR Report Key5350729
MDR Text Key35344262
Report NumberMW5059009
Device Sequence Number1
Product Code HBB
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Risk Manager
Type of Report Initial
Report Date 12/31/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model NumberMEDT T9850/C0375
Device Lot NumberA0279
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Initial Date Manufacturer Received Not provided
Initial Date FDA Received01/04/2016
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage N
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
Patient Age33 YR
Patient Weight51
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