Reported May 29, 2024 · Ongoing
Ingenia 3.0T- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device.…
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?
- Ingenia 3.0T- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device
- Model Number (REF)(1) 782103 (2) 781377 (3) 781342
- Lot codes and dates
- UDI-DI
(1) 782103 (01)00884838098299(21)(2) 781377 (01)00884838009813(21)(3) 781342 (01)00884838055339(21)
- Serial NumbersSerial Number
1,516 of 1,516 codes
851067101171152714037143371526717107181271817711017116871178711797121471252713097131371328713427141971453715507155171555715577167471693717337185971949719937199485036850458515571266713117134571392713957162871723853937121671651852087116371408714937149971541716687172971771716027126071276713247180071726
- UDI-DI
- Amount recalled
- 1517 units
This recall covers 32 products
The agency filed one notice per product. You are reading one of them; the other 31 are below.
19 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire
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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