FDA Recall Terminated

Shape-HF Cardiopulmonary Testing System Disposable Patient Interface (DPI). Part Number 0004-4001. The Shape-HF Cardiopulmonary Exercise Testing System is a stationary device that monitors parameters during laboratory or clinical conditions.

Recall: Z-1060-2015 · Initiated December 23, 2014

Recall

Recall Number
Z-1060-2015
Event Number
70149
Firm
Shape Medical Systems, Inc
FEI Number
3008072932
Product Code
BTY
Status
Terminated
Root Cause
Under Investigation by firm
Initiated
December 23, 2014
Posted
February 5, 2015
Terminated
April 14, 2015
Address
5000 Township Pkwy, Saint Paul, MN, 55110-5852

Description

Shape-HF Cardiopulmonary Testing System Disposable Patient Interface (DPI). Part Number 0004-4001. The Shape-HF Cardiopulmonary Exercise Testing System is a stationary device that monitors parameters during laboratory or clinical conditions.

Reason

This recall has been initiated because use of the impacted DPIs could result in erroneous testing results potentially leading to incorrect diagnosis and incorrect treatment. The magnitude of error for VO2 or VCO2 parameters could be approximately 20% with use of the impacted product.

Action

An Urgent Medical Device Recall letter was mailed to consignees on 12/23/2014. The letter identified affected product, described the issue and asked for product to be returned. Shape Technical Service will contact customers to assist in the return of product. A response form was asked to be returned. Customers with questions can call Shape Technical Service at 1-888-906-6266.

Distribution

Distributed in the states of AZ, FL, GA, MA, MN, NJ. NY, PA, TX, and WI.

Quantity

564 devices