FDAApril 4, 2024device

Philips IntelliSpace Cardiovascular software, Model 830089.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Study data is not able to be archived, copied, or exported with the cardiovascular software version.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

00884838115378

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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