Reported Apr 24, 2024 · Ongoing
Achieva 3.0T, 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 3.0T, Magnetic Resonance System.
- Lot codes and dates
517 of 517 codes
Model No. 781177781277781278781344781345UDI-DI n/aSerial No. 171082407024114340662405317235172561724417114340283801817049172173803317319173471709434065174303408517392173851749417384174611711917043175611745317093174141739317365172162404017035170171703917025170511700817091171261709917166171711723817189172341723317279171851725717343
- Amount recalled
- 511 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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