Reported May 28, 2025 · Ongoing
Product Name: Ingenia 3.0T CX; Model Number: 781271;
Philips North America LLC
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 Llc · 222 Jacobs St · Cambridge, MA · 02141-2289
Is this the product you have?
- Product NameIngenia 3.0T CX
- Model Number781271
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Barcodes Product as published 781271— — 00884838068452UDI-DI: 00884838068452 — Serial Numbers: 78012, 78016, 78017, 78018, 78025, 78028, 78033, 78035, 78039, 78042, 78045, 78050, 78053, 78060, 78062, 78082, 78095, 78100, 78112, 78122, 78123, 78133, 78147, 78148, 78155, 78175, 78197, 78199, 78201, 78202, 78217, 78229, 78239, 78259, 78260, 78286, 78287 - Amount recalled
- 37 units (OUS Only)
This recall covers 18 products
The agency filed one notice per product. You are reading one of them; the other 17 are below.
5 more are in the archive.
Where it was sold
- Nationwide
- GA
Why it was recalled
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
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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