inforMED
InjuryNYN

BIONICARE KNEE DEVICE

Received Aug 14, 2007 · Event occurred Jun 23, 2007

Report MW5003452 · MDR key 899874

Device

Generic name

Bionicare Knee Device

Model number

B1000

Product problems

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

Patient

YR

  • Blister(s)
  • Treatment with medication(s)

Narrative

Description of Event or Problem

AFTER USING THE DEVICE FOR A FEW HOURS, THE PT DEVELOPED BLISTERS ON HIS RIGHT KNEE AND THIGH. THE PT'S DR ADVISED HIM TO TREAT WITH OVER THE COUNTER BENADRYL.