Reported Apr 24, 2024 · Ongoing
Ingenia 3.0T 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 3.0T CX, Magnetic Resonance System.
- Lot codes and dates
346 of 346 codes
Model No. 781271782105UDI-DI 884838068452884838098312Serial No. 7800078003780047800578007780357806278010780097801178012780147801378015780167801778018780257802178019780237804378068780267805378027780287803978029780307803178032780337803478036780387804078070780427804478045780827804678047780487804978051781157805078008780587805978060780637806478065
- Amount recalled
- 342 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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