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 # Barcodes Product as published 1 Model Number (REF): 782130 2 00884838104402UDI-DI: 00884838104402 3 Serial 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.
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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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