Reported Apr 24, 2024 · Ongoing
Ingenia Elition X, Magnetic Resonance System.
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?
- Ingenia Elition X, Magnetic Resonance System.
- Lot codes and dates
456 of 456 codes
Model No. 78213678135878217782119UDI-DI 884838108622884838098336884838104129884838108608Serial No. 45051454234523845264451944535745113453224535345269452524523545178451644531645010453564506045055450024557045429453644534345236450754539845146450994502745011451004506845247451124539566001452614531545024450324513345277451524524345355451614515045245451324500045237
- Amount recalled
- 448 units
This recall covers 41 products
The agency filed one notice per product. You are reading one of them; the other 40 are below.
28 more are in the archive.
Where it was sold
- Nationwide
- GA
Why it was recalled
Patient support table floor plate may be incorrectly installed.
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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