Reported Apr 24, 2024 · Ongoing
Ingenia Elition S, 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 Elition S, Magnetic Resonance System.
- Lot codes and dates
135 of 135 codes
Model No. 781357782106UDI-DI 884838088108884838098329Serial No. 4606546071460774602546224460054600346001460084600446007460324601146012460134601546016460174601946021460024601846020460234602446046460264602746029460304603146033461094603446036460394603746052460414604246045460884605046048460494605846053460554605446061460604605746014460594604446067
- Amount recalled
- 131 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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