FDA recall Z-2767-2026

PIE Medical Imaging B.V. · Class II · device

Product

3mensio Workstation (Vascular Fenestrated) software

Reason for recall

User measurement value reported by diagnostic bioimaging software intended to measure/visualize cardiovascular structures may be larger (0.8% to 34.4%) than the actual anatomical dimension, if all the following occur: affected software is used, and the user has access only to 3D Echo OR Mitral 3D Echo, and the dataset being analyzed is a Philips 3D echo dataset containing Color Doppler information

Distribution

Worldwide - US Nationwide distribution in the states of CA, NY, MN, MI, TX and the countries of United Kingdom, Australia, France, Italy, Hong Kong SAR, Thailand, Taiwan, Netherlands, Ireland, Spain, Greece, Japan, Belgium.

Key facts

Status
Ongoing
Initiation date
2026-05-07
Report date
2026-07-29
Voluntary/Mandated
Voluntary: Firm initiated
Location
Maastricht, N/A, Netherlands

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2767-2026