inforMED
InjuryNYN

BIONICARE KNEE DEVICE

Received Oct 30, 2007 · Event occurred Oct 17, 2007

Report MW5004222 · MDR key 935943

Device

Generic name

Bionicare Knee Device

Manufacturer

Bionicare

Model number

B1000

Product problems

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

Patient

YR

  • Burn(s)

Narrative

Description of Event or Problem

THE PATIENT USED THE DEVICE ON HER LEFT LEG AND SUFFERED BURNS TO HER LEG. THE PATIENT CONTACTED HER DR WHO ADVISED HER TO IMMEDIATELY DISCONTINUE USE.