Reported Apr 24, 2024 · Ongoing
Ingenia 1.5T CX, 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 1.5T CX, Magnetic Resonance System.
- Lot codes and dates
147 of 147 codes
Model No. 781261781262UDI-DI 884838068438Serial No. Serial Number7700077002770017700477007770087701077016770197703077031770437703277033770417703477035770367703777038770397704077042770447704677091770477704877049770507705377054770597705177055770567705277057770587706077062770637706177065770697706877067770667707077072771597712777171770717707477075
- Amount recalled
- 143 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.
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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