Reported Apr 24, 2024 · Ongoing
Intera 1.5T Master/Nova, 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?
- Intera 1.5T Master/Nova, Magnetic Resonance System.
- Lot codes and dates
109 of 109 codes
Model No. 781106UDI-DI n/aSerial No. 8648865084008668884987888754860387338488892888668224836882541013183798827848280508018835682058362880087938437831389249023101341001689848325824889478479819589401053610567836490288593813610059844883458363867890188775842384108013825987008284
- Amount recalled
- 107 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.
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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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