Reported Apr 24, 2024 · Ongoing
Ingenia 1.5T, 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, Magnetic Resonance System.
- Lot codes and dates
2,252 of 2,252 codes
Model No. 781396781315782115781341782101UDI-DI 884838055322884838099715884838099043884838098275Serial No. Serial Number7005184508842434104484400845374156941104412034119570743871037089241525842837004441034844758462887057410288453884505413057061984186707526104941067414064126541409701357067670694709038481641438410574151741356841474126341463412778419261094709254101870049
- Amount recalled
- 2,242 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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