FDA Enforcement Class II Ongoing

IntelliSpace Cardiovascular software versions 6.x, 7.x, and 8.x; Model Number: 830089.

Recall: Z-1740-2025 · Reported May 14, 2025

Enforcement

Recall Number
Z-1740-2025
Event ID
96377
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Philips Medical Systems Nederland B.V.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
May 14, 2025
Initiation Date
April 7, 2025
Classification Date
May 8, 2025
Address
High Tech Campus 36, N/A, Eindhoven, N/A, N/A, Netherlands

Description

IntelliSpace Cardiovascular software versions 6.x, 7.x, and 8.x; Model Number: 830089.

Reason

An issue was identified with the software when using the Echo Module of ISCV, the issue may result in missing or incomplete information in the report.

Code Info

Model Number: 830089; Software Versions: 6x, 7.x, and 8.x; UDI-DIs: (01)00884838106970(11)211130(10)6.1.0.0 (Version 6.1.0.0), (01)00884838106970(11)220623(10)6.2.0.0 (Version 6.2.0.0), (01)00884838115378(11)221214(10)7.0.0.0 (Version 7.0.0.0), (01)00884838115378(11)230711(10)7.1.0.0 (Version 7.1.0.0), (01)00884838122000(11)240325(10)8.0.0.0 (Version 8.0.0.0).

Distribution

Domestic: Nationwide Distribution International: Australia, Austria, Belgium, Canada, Denmark, Estonia, Finland, France, Germany, Greece, Hong Kong, Indonesia, Ireland, Italy, Japan, Luxembourg, Mexico, Netherlands, Norway, Poland, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, Thailand, United Kingdom.

Quantity

996 units (267 US, 729 OUS)