FDA Adverse Event Malfunction Summary report: N

ANSPACH EMAX 2 PLUS BURR MOTOR

MDR report key: 5105217 · Received September 25, 2015

Report

Report Number
3005985723-2015-00173
Event Type
Malfunction
Date Received
September 25, 2015
Date of Event
September 1, 2015
Report Date
September 1, 2015
Manufacturer
MAKO SURGICAL CORP.
Product Code
OLO
PMA / PMN Number
K112507
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

REPORTED EVENT: ANSPACH MOTOR BEARINGS ARE BAD; BEGAN SMOKING DURING PROCEDURE. THE REPORTED EVENT WAS CONFIRMED. METHOD & RESULTS: -DEVICE EVALUATION AND RESULTS: DEVICE EVALUATION WAS PERFORMED AND THE ANSPACH EMAX 2 PLUS BURR MOTOR EVENT WAS CONFIRMED. -DEVICE HISTORY REVIEW: NOT PERFORMED AS THE ANSPACH EMAX 2 PLUS BURR MOTOR IS AN OEM PRODUCT. -COMPLAINT HISTORY REVIEW: BASED ON THE DEVICE IDENTIFICATION, THE CATSWEB AND TRACKWISE COMPLAINT DATABASES WERE REVIEWED FROM 2011 TO PRESENT FOR SIMILAR REPORTED EVENTS REGARDING OVERHEATING FAILURE OF P/N 110940 S/N: (B)(4). THERE HAVE BEEN NO OTHER EVENTS FOR THE REFERENCED SERIAL NUMBER. TREND REQUEST FOR THIS PART NUMBER HAS BEEN SUBMITTED (TREND REQUEST (B)(4)). CONCLUSIONS: THE ANSPACH EMAX 2 PLUS BURR MOTOR IS AN OEM DEVICE. UPON RECEIPT, THE DEVICE WAS EVALUATED PER (B)(4) ANSPACH EMAX 2 PLUS BURR MOTOR AND THE REPORTED EVENT WAS CONFIRMED.

Additional Manufacturer Narrative · 1

AS PART OF NORMAL COMPLAINT FOLLOW-UP, AN EVALUATION OF THE EVENT HAS BEEN INITIATED BY MAKO SURGICAL. A SUPPLEMENTAL REPORT WILL BE SUBMITTED WHEN ADDITIONAL INFORMATION BECOMES AVAILABLE.

Description of Event or Problem · 1

THE SURGEON WAS PERFORMING A PARTIAL KNEE ARTHROPLASTY USING THE ROBOTIC ARM INTERACTIVE ORTHOPEDIC SYSTEM (RIO. DURING THE CASE, THE BURR MOTOR BEGAN SMOKING. THE CASE WAS THEN COMPLETED SUCCESSFULLY.

Description of Event or Problem · 1

THE SURGEON WAS PERFORMING A PARTIAL KNEE ARTHROPLASTY USING THE ROBOTIC ARM INTERACTIVE ORTHOPEDIC SYSTEM (RIO). DURING THE CASE, THE BURR MOTOR BEGAN SMOKING. THE CASE WAS THEN COMPLETED SUCCESSFULLY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
634228 ANSPACH EMAX 2 PLUS BURR MOTOR STEREOTACTIC DEVICE OLO MAKO SURGICAL CORP.

Patients

Seq Age Sex Outcome Treatment
1 Other