Philips North America Recall: Philips SmartPath to dStream for 3.0T with MR Elastography (
Philips North America Recall: Philips SmartPath to dStream for 3.0T with MR Elastography ( is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Philips North America; Product: Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782145.; Reason for recall
| Recalling firm | Philips North America |
|---|---|
| Product | Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782145. |
| Reason for recall | The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Ongoing |
| Distribution | Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlan |
| Recall initiated | 20260414 |
| Recall number | Z-1966-2026 |
| Category | device |
| State | MA |
| Country | United States |
$29/mo
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