FDA Adverse Event Injury Summary report: N

IMPACT 754 PORTABLE VENTILATOR SYSTEM

MDR report key: 2885171 · Received December 17, 2012

Report

Report Number
2242630-2012-00112
Event Type
Injury
Date Received
December 17, 2012
Date of Event
October 20, 2012
Report Date
December 16, 2012
Manufacturer
IMPACT INSTRUMENTATION, INC.
Product Code
BTL
PMA / PMN Number
K931473
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

DEVICE WAS TESTED UPON RECEIPT AT IMPACT AND THE REPORTED PROBLEM COULD NOT BE REPLICATED THROUGH SIMULATED USE TESTING. THE DEVICE WAS DISASSEMBLED AND CORROSION ON ONE OF THE SOLDER CONNECTIONS TO THE MAIN PC BOARD WAS OBSERVED. THE UNIT SHOWED EXTENSIVE EXTERNAL DAMAGE INDICATING POTENTIAL MISUSE OF THE DEVICE WHICH MAY HAVE CAUSED FLUID INGRESS AND CORROSION. REPAIR OF THE EXTERNAL DAMAGE AND THE INTERNAL CORROSION ISSUE WAS EXECUTED. PERIODIC MAINTENANCE WAS PERFORMED INCLUDING CALIBRATION AND BURN-IN AND THE UNIT WAS RETURNED TO THE END USER AFTER IT TESTED WITHIN SPECIFICATIONS.

Description of Event or Problem · 1

PATIENT WAS BEING SUPPORTED ON AN IMPACT 754 PORTABLE VENTILATOR SYSTEM AND IT WAS REPORTED THAT THE VENTILATOR SCREEN TURNED BLACK AND THE UNIT STOPPED WORKING. THE END USER REPORTED THERE WAS NO SERIOUS INJURY TO THE PATIENT AS A RESULT OF THE INCIDENT. THOUGH IT WAS REPORTED THAT SERIOUS INJURY TO THE PATIENT DID NOT OCCUR, AND, THOUGH IT WAS NOT REPORTED THAT BACK-UP EQUIPMENT WAS USED, WE HAVE SUBMITTED THIS AS A SERIOUS INJURY EVENT BECAUSE BACK-UP VENTILATION EQUIPMENT MAY HAVE BEEN NECESSARY TO PRECLUDE PERMANENT IMPAIRMENT OR DAMAGE DUE TO THE UNEXPECTED DEVICE ACTIVITY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 IMPACT 754 PORTABLE VENTILATOR SYSTEM VENTILATOR BTL IMPACT INSTRUMENTATION, INC. 754 NA

Patients

Seq Age Sex Outcome Treatment
1 Other| R NONE REPORTD BY THE OPERATOR