Pages

Friday, July 21, 2017

US FDA News: Penumbra 3D Revascularization Device by Penumbra: Class I Recall - Wire Material May Break or Separate During Use

Fractured pieces of the delivery wire could be left inside the patient’s brain bloodstream. This or the attempts made to retrieve the fractured pieces can lead to serious adverse health consequences.
Read more: Penumbra 3D Revascularization Device by Penumbra: Class I Recall - Wire Material May Break or Separate During Use