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FDA Device recall Z-1987-2012

IntelliSpace Portal software and Extended Brillance Workspace software Intellispace Portal is a multimodality thin-client applications serv…

On 2012-07-18 the FDA classified a Class II recall of IntelliSpace Portal software and Extended Brillance Workspace software Intellispace Portal is a multimodality thin-client applications serv… by Philips Medical Systems Cleveland, citing the Intellispace Portal software and Extended Brillance Workspace software may have significantly different results in the colors and size of the affected area when the customer u….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1987-2012
ClassificationClass II
Statusterminated
Initiated2012-05-23
Published2012-07-18
Last updated2026-09-13 11:53 UTC
CompanyPhilips Medical Systems Cleveland
DistributionUS

Product

IntelliSpace Portal software and Extended Brillance Workspace software Intellispace Portal is a multimodality thin-client applications server that delivers full diagnostic viewing and clinical applications to the enterprise. The Philips Extended Brillance Workspace is intended for use as a diagnostic viewing and processing workstation.

Reason

The Intellispace Portal software and Extended Brillance Workspace software may have significantly different results in the colors and size of the affected area when the customer uses the "Time Sensitive" and "Time Insensitive" methods.

Identifiers

code_info
Model number: 881001; serial numbers: 85104, 80818, 85088, 82038, 81013, 80911, 82017, 80994, 81021, 81017, 81065, 8116…Model number: 881001; serial numbers: 85104, 80818, 85088, 82038, 81013, 80911, 82017, 80994, 81021, 81017, 81065, 81161, 81164, 81130, 81004, 81003 & 80979. Model number: 728260; serial numbers: 10102, 6483, 14691, 10155, 12050, 11169, 15016, 15677, 15658, 14834, 14955, 10173, 15018, 14171, 14170, 11994 & 11995.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1987-2012%22

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