Reported Apr 24, 2024 · Ongoing
SmartPath to dStream for XR and 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?
- SmartPath to dStream for XR and 3.0T, Magnetic Resonance System.
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Barcodes Product as published 781270782113, 782129 — 884838098909884838105805UDI-DI 884838098909, 884838105805 — Serial No. 17271, 38281, 17560, 17252, 34202, 34153, 34127, 38311, 34128, 34172, 17470, 34131, 24021, 24093, 17258, 38290, 35041, 38105, 34110, 17449, 38010, 34212, 38142, 34117, 38166, 38106, 34129, 38310, 38195, 38219, 24077, 24039, 38222, 17521, 34072, 38117, 38070, 34055, 17439, 17455, 38075. - Amount recalled
- 41 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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