Reported Oct 2, 2024 · Ongoing
Ingenia 1.5T -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of…
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?
3 of 3 products
| # | Product as published |
|---|---|
| 1 | 782115 |
| 2 | 782101 |
| 3 | 782140 |
- Lot codes and dates
- Model UDI-DI
782115 (01)00884838099043(21)782101 (01)00884838098275(21)782140 (01)00884838108646(21)
- Serial Numbers
456016129161312613156132861336613376133961348613496135161354613556135661357613596136061361613626136361364613676137161373613746137561376613776137861380613836138461394613956139761403614046140661407614126141561416876458764887649876518765487655
- Model UDI-DI
- Amount recalled
- 48 units
This recall covers 13 products
The agency filed one notice per product. You are reading one of them; the other 12 are below.
Where it was sold
- Nationwide
Why it was recalled
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.
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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