Reported Apr 24, 2024 · Ongoing
Ingenia 1.5T 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 1.5T S, Magnetic Resonance System.
- Lot codes and dates
137 of 137 codes
Model No. 781347UDI-DI 884838068421Serial No. 81034810338101581113810808110381137810018100381004810148100781006810098101081011810628102081016810178101881019810238102581024810278102881030810318103281035810568103781057810558106081038810408104181043810448104781045810398105081051810528106181063810648106581074810678107981069810708111681071
- Amount recalled
- 135 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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