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FDAJanuary 4, 2016device

Philips IntelliVue Module Measurement X2 Model: M3002A

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

The hazard

The ST elevation alarm on the Patient Monitor or standalone X2 Measurement Module will not sound when indicated for all chest leads derived using Hexad 12-Lead ECG Monitoring in the Host Monitor

What to do

FDA enforcement status: Terminated

Brands named

philips electronics north americaphilipsphilips electronics

Recall history

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

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Philips IntelliVue Module Measurement X2 Model: M3002A — Recall Details · AllClear