inforMED
OtherFII

MDR event

Received Nov 9, 2007

Report 9616240-2007-00103 · MDR key 956601

Device

Product problems

  • Normal
  • Unknown (for use when the device problem is not known)

Patient

Not reported

  • Death

Narrative

Additional Manufacturer Narrative

AS A RESULT OF GAMBRO'S COMPLAINT INVESTIGATION, GAMBRO HAS FOUND NO MALFUNCTION OF THE PHOENIX SYSTEM AND NO EVIDENCE TO SUGGEST THAT ANY GAMBRO DEVICE CAUSED OR CONTRIBUTED TO THIS EVENT.