Reported May 29, 2024 · Ongoing
Ingenia 3.0T CX Model Number (REF): (1) 782105 (2) 781271
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
- CX Model Number (REF)(1) 782105 (2) 781271
- Lot codes and dates
- UDI-DI(1) (01)00884838098312(21); (2) (01)00884838068452(21) Serial Number
349 of 349 codes
781217815078157780967820878094780127807478154781617817078171781727817378182781837818978190781967819878205782107821278213782167821878221782257823378235782387824078241782427824378244782507825178252782537825678257782627826378265782667826778268782697827078271782727827378279782807828178282782837828478288
- UDI-DI(1) (01)00884838098312(21); (2) (01)00884838068452(21) Serial Number
- Amount recalled
- 350 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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