Reported Aug 6, 2025 · Ongoing
Ingenia 3.0T CX Model Numbers (REF): (1) 781271, (2) 782105;
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?
- Ingenia 3.0T
- CX Model Numbers (REF)
(1) 781271(2) 782105
- Lot codes and dates
- Model Numbers (REF)
(1) 781271(2) 782105
- UDI-DI
(1) 00884838068452(2) 00884838098312
- Serial Numbers
350 of 350 codes
(1) 780007800378004780057800778008780097801078011780127801378014780157801678017780187801978021780227802378025780267802778028780297803078031780327803378034780357803678038780397804078042780437804478045780467804778048780497805078051780537805878059780607806278063780647806578066780677806878070780717807278073
- Model Numbers (REF)
- Amount recalled
- 350 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.
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