Reported Apr 24, 2024 · Ongoing
Achieva XR, 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?
- Achieva XR, Magnetic Resonance System.
- Lot codes and dates
Model No. 781153781253UDI-DI n/aSerial No. 35075230282301723021350063501535016350212300923003230312300523035230403500735022350253502835024350353503935049350553501335064350633507135068350693507035067350813501135083350843508223020230383507635020350853505035057230143500435061350742300423029
- Amount recalled
- 49 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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