Reported Jun 21, 2017 · Terminated
Philips DuraDiagnost X-ray systems: DuraDiagnost (R1.0, Product Number 712210) DuraDiagnost (R2.0, Product Number…
Philips Electronics North America Corporation
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 Electronics North America Corporation · 3000 Minuteman Rd · Andover, MA · 01810-1032
Is this the product you have?
- Philips DuraDiagnost X-ray systems
DuraDiagnost (R1.0Product Number 712210) DuraDiagnost (R2.0Product Number 712211) DuraDiagnost (R3.0Product Number 712211)
- Lot codes and dates
SN120001-SN120003SN130001-SN130023SN140001-SN140022SN140024SN140027SN140030-SN140031SN140033-SN140046SN140048SN140050-SN140068SN150001-SN150004SN150006SN150008-SN150011SN160001SN160002
- Amount recalled
- 98 sytems
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Why it was recalled
Tube arm assembly could fall down due to cracked welding joints
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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