Reported Mar 6, 2019 · Terminated

Prodiva CX, Model Number 781070. Nuclear Magnetic Resonance Imaging System

Philips Medical Systems Nederlands

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Philips Medical Systems Nederlands · Veenpluis 4-6 · Best · N/A

Is this the product you have?

  • Prodiva CX, Model Number 781070. Nuclear Magnetic Resonance Imaging System
Lot codes and dates
  • All systems
Amount recalled
11226 total

This recall covers 64 products

The agency filed one notice per product. You are reading one of them; the other 63 are below.

51 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Nov 19, 2020 · Data as of Sep 19, 4:51 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.