Philips Fetal Spiral Electrode Recall: Metal Tip Breaks Off in Newborn Scalp

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Recalling firmPhilips North America, LLC3000 Minuteman Rd, N/A · Andover, MA 01810-1032

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Philips is recalling a specific fetal electrode model because it can break off during delivery and stay in a newborn's scalp. This poses a serious risk to infants during birth.

Why it’s dangerous

The metal electrode tip can break off during delivery and remain in the newborn's scalp. This could cause injury or complications for the baby. The hazard occurs during normal use in labor and delivery settings.

Who’s affected

Newborns delivered using this specific Philips fetal electrode model are at risk. Healthcare providers using the device during labor and delivery are most affected.

How to tell if you have this one

Check for model number 9898 031 :37631 on the device. All products currently in distribution are affected. This recall applies to newborns delivered using this specific electrode model.

Brand
Philips
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Stop Using Now
Immediately stop using the Philips Fetal Spiral Electrode model 9898 031 37631 if it is in use during delivery.

✎ GovInfoNow

Questions people ask

Is this electrode safe for newborns?

The recall states the electrode can break off and remain in the scalp, so it is not safe for newborns during delivery.

How can I check if I have the recalled model?

Look for model number 9898 031 37631 on the device. All products currently in distribution are affected.

What should I do if I have this electrode?

The recall requires stopping use immediately and contacting Philips for guidance.

Take action

Contact Philips

We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1250-2019 — Philips Philips

Hello,

I own a Philips that is covered by recall Z-1250-2019 from Philips.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-1250-2019 (January 25, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1250-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Philips North America, LLC recalls Fetal Spiral Electrode, Model No. 9898 031 37631

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