Z-2069-2012 Class II Terminated

Recalled by AGFA Corp. — Greenville, SC

FDA device recall Z-2069-2012 was initiated by AGFA Corp. on July 10, 2012 and is designated Class II. Reason for recall: When users selected "Left stenosis" in the "Graft Duplex Conclusion" section in IMPAX CV Reporting Non-Invasive(NIV) module, "Right stenosis" appeared in the sentence display within the printed repres… The recall status is terminated (terminated October 29, 2013). Affected quantity: 6.

Recall Details

Product Type
Devices
Report Date
August 1, 2012
Initiation Date
July 10, 2012
Termination Date
October 29, 2013
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
6

Product Description

IMPAX CV Reporting The Results Management (RM)/IMPAX CV reporting component facilitates the quick, effective creating of digital structured reports for : adult catheterization and echocardiography, pediatric echocardiography, congenital heat disease, nuclear cardiology and non-invasive vascular disease management. This webb-based application allows cardiology departments to view, edit and sign the structured reports.

Reason for Recall

When users selected "Left stenosis" in the "Graft Duplex Conclusion" section in IMPAX CV Reporting Non-Invasive(NIV) module, "Right stenosis" appeared in the sentence display within the printed representation of the report.

Distribution Pattern

Nationwide Distribution including IN, SC, OH, TX

Code Information

Software Version: RM 2.03 to 2.08, NIV 1.0