FDA Recall Terminated

IMPAX Cardiovascular The IMPAX CV Reporting module consists of a database and graphical user interface (GUI) that allows users to document procedure and clinical findings as structured data, with representation in printed or electronic formats

Recall: Z-2652-2017 · Initiated December 22, 2016

Recall

Recall Number
Z-2652-2017
Event Number
77629
Firm
AGFA Healthcare Corp.
FEI Number
3001236302
Product Code
LLZ
Status
Terminated
Root Cause
Software design
Initiated
December 22, 2016
Terminated
August 27, 2021
Address
10 S Academy St, Greenville, SC, 29601-2632

Description

IMPAX Cardiovascular The IMPAX CV Reporting module consists of a database and graphical user interface (GUI) that allows users to document procedure and clinical findings as structured data, with representation in printed or electronic formats

Reason

A customer experienced when using IMPAX CV Reporting software, specifically, when building a NIV report, the NIV Cardio report was showing incorrect findings for Aneurysm.

Action

AGFA Healthcare sent an Urgent Field Safety Notice dated December 22, 2016, to all affected consignees. The notice included an acknowledgement fax-back or email indicating that the information was received and understood. The notice informed the consignees of the problem and indicated that they would be contacted by Agfa Service to check the problem and to correct the NIV reporting clinical content. Customers with questions were instructed to call 1-401-330-7433. For questions regarding this recall call 864-421-1984.

Distribution

Nationwide Distribution to NJ, NC, OH, PA, SC, TN, TX, and WI

Quantity

10