FDA Adverse Event Malfunction Summary report: N

LEGEND FOOTED ATTACHMENT

MDR report key: 1881345 · Received October 7, 2010

Report

Report Number
1625507-2010-00057
Event Type
Malfunction
Date Received
October 7, 2010
Date of Event
August 1, 2010
Report Date
September 8, 2010
Manufacturer
MDT POWERED SURGICAL SOLUTIONS
Product Code
HBB
PMA / PMN Number
K020069
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

REPORT CONFIRMED. EVALUATION DETERMINED THAT THE FOOTED PORTION WAS DAMAGED BY TOOL CONTACT. NO ADD¿L INFO WAS AVAILABLE ON F/U. EVENT DATE ESTIMATED. THE USER MANUAL CONTAINS THE FOLLOWING WARNING "THE ATTACHMENT SHOULD NOT BE USED IF ANY PART OF THE ATTACHMENT APPEARS TO BE BENT, LOOSE, MISSING, OR DAMAGED. EXCESSIVE PRESSURE OR IMPROPER HANDLING, SUCH AS BENDING OR PRYING, OF THE ATTACHMENT OR DISSECTING TOOL MAY CAUSE INJURY TO THE PT, OPERATOR AND/OR OPERATING ROOM STAFF."

Description of Event or Problem · 1

DEVICE RETURNED FOR NON-SPECIFIED REPAIR. NO PT IMPACT REPORTED. REPAIR REQUEST ESCALATED TO COMPLAINT ON EVALUATION DUE TO ATTACHMENT FOOT BEING DAMAGED BY TOOL CONTACT. NO ADD¿L INFO WAS AVAILABLE ON F/U.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LEGEND FOOTED ATTACHMENT HBB - MOTOR, DRILL, PNEUMATIC HBB MDT POWERED SURGICAL SOLUTIONS NA NA

Patients

Seq Age Sex Outcome Treatment
1