Reported Nov 15, 2023 · Ongoing
DigitalDiagnost C90 Release 3, used to acquire, process, store, display and export digital radiographic images.
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 Release 3, used to acquire, process, store, display and export digital radiographic images.
- Lot codes and dates
Model No. 712025Serial No. SN13000328
- Amount recalled
- 1 unit
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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