inforMED
InjuryNYN

BIONICARE KNEE DEVICE

Received Aug 14, 2007 · Event occurred Apr 10, 2007

Report MW5003451 · MDR key 899871

Device

Generic name

Bionicare Knee Device

Model number

B1000

Product problems

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

Patient

YR

  • Rash
  • Therapy/non-surgical treatment, aborted/stopped
  • Treatment with medication(s)

Narrative

Description of Event or Problem

AFTER USING THE DEVICE FOR SEVERAL MONTHS, THE PT DEVELOPED A LARGE RASH ON HIS RIGHT THIGH. THE PT'S DR PRESCRIBED PREDNISONE FOR THE RASH, AND THE PT DISCONTINUED USE OF THE DEVICE. THE PT CALLED IN TO MEDICAL WHEN THE RASH HEALED AND WAS SENT ALOE VERA GEL TO USE WITH THE DEVICE.