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FDA (Device enforcement)Recalled 2024-09-03class ii

Philips North America Llc: SmartPath to dStream for XR and 3.0T- For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the h

Hazard

Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and protrude beyond the surface could cause the screws to interfere with other moving parts, potentially blocking the horizontal tabletop. May lead to delay in diagnosis and/or may include anxiety of a patient is left on the tabletop inside the bore for a longer duration than anticipated. movement.

Details from the source

Reason for recall: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and protrude beyond the surface could cause the screws to interfere with other moving parts, potentially blocking the horizontal tabletop. May lead to delay in diagnosis and/or may include anxiety of a patient is left on the tabletop inside the bore for a longer duration than anticipated. movement. Distribution: Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Belgium, Brazil, Canada, Chile, China, Colombia, Croatia, Czech Republic, Denmark, Ecuador, Egypt, Finland, France, Germany, Iceland, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Jordan, Kuwait, Latvia, Maldives, Mauritius, Mexico, Morocco, Netherlands, Pakistan, Peru, Poland, Portugal, Qatar, Romania, Russian Quantity: 14 units Lot/code info: Model UDI-DI: 782113 (01)00884838098909(21); 781270 (01)00884838095083(21); 782129 (01)00884838105805(21). Serial Numbers: 17271 17389 17439 17449 17504 24039 24077 34055 34072 34129 34262 38117 38166 38222

UPC codes

00884838098909, 00884838095083, 00884838105805

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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