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FDAJanuary 25, 2019device

Fetal Spiral Electrode, Model No. 9898 031 37631

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

The hazard

During use of the Philips FSE, it is possible for the metal electrode tip to break off and remain in the scalp of the newborn following labor and delivery.

What to do

FDA enforcement status: Terminated

Brands named

philips north americaphilipsphilips north

UPCs

989803137631

Recall history

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

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Fetal Spiral Electrode, Model No. 9898 031 37631 — Recall Details · AllClear