FDA Adverse Event Malfunction Summary report: N

VISUM LED II SURGICAL LIGHT

MDR report key: 2481263 · Received February 22, 2012

Report

Report Number: 2031963-2012-00015
Event Type: Malfunction
Date Received: February 22, 2012
Date of Event: January 25, 2012
Report Date: January 25, 2012
Manufacturer: STRYKER COMMUNICATIONS
Product Code: FSY
PMA / PMN Number: K060802
Product Problem: Yes
Report Source: Manufacturer report
Reporter Location: WI, US
Reporter Occupation: OTHER

Narratives

Additional Manufacturer Narrative · 1

THERE WAS NO REPORTED PT INVOLVEMENT, THEREFORE, NO PT DATA EXISTS. CAMERA COVERS FROM EARLIER REPORTS WITH THE CRACKED GLASS CONDITION HAVE BEEN RETURNED TO THE MFR AND VISUALLY EVALUATED. FURTHERMORE, A STRYKER ENGINEER VISITED THE CUSTOMER ACCOUNT FOR ADD'L EVAL. ADD'L INVESTIGATION IS ONGOING. THE CATALOG NUMBER PROVIDED IS FOR THE IN-LIGHT CAMERA COVER WHICH IS THE COMPONENT IDENTIFIED AS ALLEGEDLY MALFUNCTIONING. EVAL SUMMARY: THE GLASS OF THE STERILIZABLE IN-LIGHT CAMERA COVERS WAS REPORTED TO HAVE SHOWN SIGNS OF CRACKING. SAMPLES OF THESE CRACKED CAMERA COVERS HAVE BEEN RETURNED TO THE MFR AND VISUALLY EVALUATED. FURTHERMORE, A STRYKER ENGINEER VISITED THE CUSTOMER ACCOUNT FOR ADD'L EVAL REGARDING THE USE, CLEANING, AND STERILIZING OF THE CAMERA COVERS BUT NO CONCLUSION AS TO THE CAUSE OF THIS REPORTED EVENT CAN BE DETERMINED AT THIS TIME. THE INVESTIGATION IS ONGOING. THERE WAS NO PT INVOLVEMENT AND NO REPORT OF ANY ADVERSE CONSEQUENCES TO THE PT OR CAREGIVER. THIS IS NOT A SINGLE USE DEVICE.

Description of Event or Problem · 1

(B)(4). IT WAS REPORTED THAT AN IN-LIGHT CAMERA COVER HAS SHOWN SIGNS OF THE GLASS CRACKING. THERE WAS NO PT INVOLVEMENT REPORTED AND NO ADVERSE CONSEQUENCE REPORTED.

Devices

Seq	Brand	Generic	Product Code	Manufacturer	Model	Lot	UDI-DI
1	VISUM LED II SURGICAL LIGHT		FSY	STRYKER COMMUNICATIONS

Patients

Seq	Age	Sex	Outcome	Treatment
1