Intervalve recalls

Intervalve appears in 1 official U.S. recall notice indexed by RecallRadar, most recently on 2014-05-21.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• InterValve V8 Balloon Aortic Valvuloplasty Catheter, model 172212C110, 192412C110, 212612C110, 232812C110
  FDA Device · Class II · 2014-05-21 · Intervalve