Reported Apr 23, 2025 · Ongoing
Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.
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?
- Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.
- Lot codes and dates
- REF 712214
- UDI
(01)00884838064751(21)Serial No. SN170009SN170010SN180072SN180020 200037SN160061SN180075200089SN180045SN160096
- Amount recalled
- 83 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Potential for collimator to fall as a result of incorrect installation.
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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