Reported Aug 6, 2025 · Ongoing

Upgrade to MR 7700 Model Number (REF): 782130;

Philips North America

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 North America · 222 Jacobs St · Cambridge, MA · 02141-2296

Is this the product you have?

  • Upgrade to MR 7700 Model Number (REF)782130
Lot codes and dates

3 of 3 products

Products covered by this recall
#BarcodesProduct as published
1Model Number (REF): 782130
200884838104402UDI-DI: 00884838104402
3Serial Numbers: 42030, 42037, 42066, 42151, 42163, 42164, 42211, 42219, 42248, 42376, 45001, 45007, 45051, 45052, 45179, 45236, 45297, 45298, 45301, 45552, 45555, 71613, 71907, 85394, 85643, 85644
Amount recalled
26 units

This recall covers 19 products

The agency filed one notice per product. You are reading one of them; the other 18 are below.

6 more are in the archive.

Where it was sold

  • Nationwide
  • GA

Why it was recalled

The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.

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.

Free recall alerts

Get alerted about new produce recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:39 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.