FDA Adverse Event Malfunction Summary report: N

2.7 DEGREE STRAIGHT SAGITAL SAW

MDR report key: 9446915 · Received December 10, 2019

Report

Report Number
3005985723-2019-00894
Event Type
Malfunction
Date Received
December 10, 2019
Date of Event
November 13, 2019
Report Date
March 18, 2020
Manufacturer
MAKO SURGICAL CORP.
Product Code
OLO
UDI-DI
00848486032111
PMA / PMN Number
K143752
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CT, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

REPORTED EVENT: EXTREMELY LOUD WHEN CUTTING. CASE TYPE: TKA SURGICAL DELAY: 16-30 MINUTES. PRODUCT EVALUATION AND RESULTS: THE PRODUCT WAS NOT EVALUATED AS THE PRODUCT WAS UNAVAILABLE FOR INSPECTION CAPA 2127499 HAS BEEN RAISED FOR THE SAME. PRODUCT HISTORY REVIEW: REVIEW OF THE DEVICE HISTORY RECORDS INDICATE 20 DEVICES WERE MANUFACTURED AND 20 WERE ACCEPTED INTO FINAL STOCK ON 11/12/2018 WITH NO REPORTED DISCREPANCIES. COMPLAINT HISTORY REVIEW: A REVIEW OF COMPLAINTS IN CATSWEB AND TRACKWISE RELATED TO P/N 212186, LOT 35041018 SHOWS 0 ADDITIONAL COMPLAINTS RELATED TO THE FAILURE IN THIS INVESTIGATION. CONCLUSIONS: THE FAILURE COULD NOT BE DETERMINED AS THE PRODUCT WAS NOT AVAILABLE FOR INSPECTION. NO ADDITIONAL INVESTIGATION OR SPECIFIC ACTIONS ARE REQUIRED. IF ADDITIONAL INFORMATION IS RECEIVED THEN THE COMPLAINT WILL BE REOPENED. CORRECTIVE ACTION/PREVENTIVE ACTION: A REVIEW OF STRYKER¿S NC/CAPA DATABASE INDICATED THERE HAVE BEEN NO NC AND CAPA ASSOCIATED WITH THE PRODUCT AND FAILURE MODE REPORTED IN THIS EVENT.

Description of Event or Problem · 0

EXTREMELY LOUD WHEN CUTTING. CASE TYPE: TKA. SURGICAL DELAY: 16-30 MINUTES.

Additional Manufacturer Narrative · 1

AS PART OF THE 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. NOT RETURNED.

Description of Event or Problem · 1

EXTREMELY LOUD WHEN CUTTING. CASE TYPE: TKA. SURGICAL DELAY: 16-30 MINUTES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1238076 2.7 DEGREE STRAIGHT SAGITAL SAW STEREOTAXIC DEVICE, ROBOTICS OLO MAKO SURGICAL CORP. 212186 35041018 00848486032111

Patients

Seq Age Sex Outcome Treatment
1 Other