Reported Apr 24, 2024 · Ongoing
SmartPath to dStream for 1.5T, 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?
- SmartPath to dStream for 1.5T, Magnetic Resonance System.
- Lot codes and dates
676 of 676 codes
Model No. 781260782112UDI-DI 884838095076884838098886Serial No. 89541872632174216648906857810703883510154897120226900121665202042110854751203339024101963213186301203487728091215552129418561187611048218800222858560217881106430146810010036130522102321290320942122310717321421213455728378210033910385668190552310511216112161221888
- Amount recalled
- 672 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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