Reported Apr 24, 2024 · Ongoing
Ingenia 3.0T, 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, Magnetic Resonance System.
- Lot codes and dates
1,515 of 1,515 codes
Model No. 781377781342782103UDI-DI 884838009813884838055339884838098299Serial No. 420037133642370710224236842117420664205242040422427139942241420994212642127710454225842033851544235285655422487173971829714954230771038422867181042247711854215271449421044200642158421594216071331713827131271907421167168371062424164210942293420314209842193421027119385665
- Amount recalled
- 1,509 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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