Reported Nov 15, 2023 · Ongoing
DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, process, store, display and export digital radiographic…
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?
- DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, process, store, display and export digital radiographic images.
- Lot codes and dates
- Model No. 712035
- UDI
66 of 66 codes
(01)00884838090705(21)10000009(01)00884838090705(21)10000010(01)00884838090705(21)10000003(01)00884838090705(21)10000004(01)00884838090705(21)10000002(01)00884838090705(21)10000001(01)00884838090705(21)10000053(01)00884838090705(21) 10001042(01)00884838090705(21) 10001044(01)00884838090705(21) 10001125(01)00884838090705(21) 10001113(01)00884838090705(21) 10001111(01)00884838090705(21) 10001112(01)00884838090705(21) 10001109(01)00884838090705(21) 10001110(01)00884838090705(21) 10001114(01)00884838090705(21) 21862107(01)00884838090705(21) 10001130(01)00884838090705(21) 21862103(01)00884838090705(21) 21862101(01)00884838090705(21) 21862100(01)00884838090705(21) 22860370(01)00884838090705(21) 21862123(01)00884838090705(21) 21862126(01)00884838090705(21) 22860323(01)00884838090705(21) 22860045(01)00884838090705(21) 22860317(01)00884838090705(21) 22860316(01)00884838090705(21) 22860318(01)00884838090705(21) 22860342(01)00884838090705(21) 22860357(01)00884838090705(21) 23860320(01)00884838090705(21) 23860316Serial No. 100000091000001010000003100000041000000210000001100000531000104210001044100011251000111310001111100011121000110910001110100011142186210710001130218621032186210121862100228603702186212321862126228603232286004522860317
- Amount recalled
- 33 units
This recall covers 10 products
The agency filed one notice per product. You are reading one of them; the other 9 are below.
Where it was sold
- Nationwide
Why it was recalled
Potential for units suspended on the ceiling to fail and fall.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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