FDA Recall Terminated

Innocor Cardiopulmonary Exercise and Lung Function Testing System Non-invasive diagnostic device that measures or calculates a number of hemodynamic and metabolic parameters.

Recall: Z-2769-2016 · Initiated May 13, 2016

Recall

Recall Number
Z-2769-2016
Event Number
74649
Firm
Innovision A/S Skovvaenget 2 Glamsbjerg Denmark
FEI Number
1000334329
Product Code
BZC
Status
Terminated
Root Cause
Device Design
Initiated
May 13, 2016
Posted
September 8, 2016
Terminated
February 10, 2017

Description

Innocor Cardiopulmonary Exercise and Lung Function Testing System Non-invasive diagnostic device that measures or calculates a number of hemodynamic and metabolic parameters.

Reason

The purpose of the recall is to replace data transmission cable (USB-cable) connecting the lnnocor device with an external computer. The replacement USB cable will provide galvanic isolation of the lnnocor from the external computer via opto-couplers, as opposed to the grounding protection currently in use. The replacement is intended to prevent risk of electric shock.

Action

Recall notifications described the issue and actions to be taken by the firm. The notice also stated that replacement costs would be carried by Innovision ApS. Acknowledgment of the notice can be made by contacting service manager Knud Pedersen at [email protected] or (+45) 65 95 91 00) to schedule the service activity and to answer any questions.

Distribution

Worldwide Distribution -- US, to Massachusetts and Washington, DC; and, the countries of Canada, Germany, and United Kingdom.

Quantity

8