FDA Adverse Event Other Summary report: N

UNI-VENT

MDR report key: 2439707 · Received January 28, 2012

Report

Report Number
2242630-2005-00029
Event Type
Other
Date Received
January 28, 2012
Date of Event
April 21, 2005
Report Date
June 17, 2005
Manufacturer
IMPACT INSTRUMENTATION, INC.
Product Code
BTL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

DATE NOTIFIED: (B)(4) 2005. A MODEL 706 VENTILATOR (S/N (B)(4)) FAILED TO CYCLE. AN INSPECTION OF THE DEVICE REVEALED A DEFECTIVE RESISTOR AND A DEFECTIVE INTEGRATED CIRCUIT. THE RESISTOR AND THE IC WERE REPLACED. THE DEVICE WAS TESTED TO SPECIFICATIONS AND RETURNED TO THE CUSTOMER. NO PT WAS INVOLVED AT THE TIME OF THE FAILURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 UNI-VENT VENTILATOR BTL IMPACT INSTRUMENTATION, INC. 706

Patients

Seq Age Sex Outcome Treatment
1 NA Other