Philips Chest Pneumograph Recall: Natural Rubber Latex Not Listed on Label

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

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Philips is recalling chest pneumographs made since 1:1996 because they don't list natural rubber latex on their labels. This could cause allergic reactions in people sensitive to latex.

Why it’s dangerous

The chest pneumograph contains natural rubber latex, but the label doesn't state this. People with latex allergies could have reactions like rashes or breathing problems if they come into contact with the device.

Who’s affected

Healthcare professionals using the chest pneumograph for MRI scans are most at risk. People with latex allergies may react to the device.

How to tell if you have this one

Check for the product name 'Chest Pneumograph' or 'pneumatic bellows' on the label. The device was made since 1996 with part number 94023.

Brand
Philips
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Label for Latex Warning
Look for a statement that the product contains natural rubber latex on the label.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The product may cause allergic reactions in people sensitive to natural rubber latex. Check the label for a warning.

What should I do if I have latex allergies?

If you have latex allergies, contact Philips for advice on alternatives or safety measures.

When was this product first made?

The product was first made in 1996.

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-2245-2020 — Philips Philips

Hello,

I own a Philips that is covered by recall Z-2245-2020 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-2245-2020 (April 13, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2245-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.

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