FDA Adverse Event Malfunction Summary report: N

ANSPACH EMAX 2 PLUS BURR MOTOR

MDR report key: 6934194 · Received October 10, 2017

Report

Report Number
3005985723-2017-00492
Event Type
Malfunction
Date Received
October 10, 2017
Date of Event
September 26, 2017
Report Date
January 4, 2018
Manufacturer
MAKO SURGICAL CORP.
Product Code
OLO
PMA / PMN Number
K170584
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

FOLLOW-UP #1 AND FINAL REPORT SUBMITTED TO UPDATE SECTIONS BASED ON THE RESULTS OF INVESTIGATION. REPORTED EVENT: ANSPACH EMAX 2 PLUS BURR MOTOR STARTED SMOKING. 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 ANSPACH EMAX 2 PLUS BURR MOTOR STARTED SMOKING FAILURE OF P/N: 110940, S/N: (B)(4). THERE HAVE BEEN NO OTHER SIMILAR EVENTS FOR THE REFERENCED SERIAL NUMBER. CONCLUSIONS: THE ANSPACH EMAX 2 PLUS BURR MOTOR IS AN OEM DEVICE. UPON RECEIPT, THE ANSPACH EMAX 2 PLUS BURR MOTOR WAS BENCH EVALUATED BY (B)(4) AND THE REPORTED EVENT WAS CONFIRMED. CORRECTIVE ACTION/PREVENTIVE ACTION: AS THE EVENT DID NOT INVOLVE A MANUFACTURING RELATED PRODUCT PROBLEM INDICATING A NON-CONFORMITY, ADVERSE TREND, OR UNANTICIPATED HAZARD, NO CORRECTIVE ACTION IS REQUIRED AT THIS TIME.

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

ANSPACH MOTOR STARTED SMOKING DURING A DEMO PKA.

Description of Event or Problem · 1

ANSPACH MOTOR STARTED SMOKING DURING A DEMO PKA.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
717394 ANSPACH EMAX 2 PLUS BURR MOTOR STEREOTAXIC DEVICE, ROBOTICS OLO MAKO SURGICAL CORP.

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization