Reported Aug 6, 2025 · Ongoing
Achieva XR; Model Numbers (REF): (1) 781153, (2) 781253;
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?
- Achieva XR
- Model Numbers (REF)
(1) 781153(2) 781253
- Lot codes and dates
- Model Numbers (REF)
(1) 781153(2) 781253
- UDI-DI
(1) None(2) None
- Serial Numbers
(1) 23003230042300523011230142301723020230212302823031230352304134039(2) 350043500635007350113501535016350193502035021350223502835035350493505035061350633506735068350693507035074350753507635081350833508435085
- Model Numbers (REF)
- Amount recalled
- 40 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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