Reported Apr 24, 2024 · Ongoing
MR 5300, 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?
- MR 5300, Magnetic Resonance System.
- Lot codes and dates
168 of 168 codes
Model No. 782110UDI-DI 884838099364Serial No. 63029630876301463103630006300663007630016300863010630136301563021630226303963023630246302663025630286303063031630386305463041630426304663043630446304763049630506301263051630536303263057630606309463064630636306863079630666307263071630706308263074630766308363202630856301963086630936309163090
- Amount recalled
- 166 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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