Ekos recalls

Ekos appears in 6 official U.S. recall notices indexed by RecallRadar, most recently on 2016-10-05.

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

• The EKOS cart has the catalog number 700-60101
  FDA Device · Class II · 2016-10-05 · Ekos
• EkoSonic Endovascular Devices EKOS Intelligent Drug Delivery Catheter
  FDA Device · Class II · 2016-09-28 · Ekos
• EkoSonic Endovascular System, Catalog Number 500-56112
  FDA Device · Class II · 2016-03-02 · Ekos
• The EKOS EkoSonic Control Unit is intended exclusively for use with the EkoSonic Endovascular Device and the EkoSonic MACH4 Endovascular De…
  FDA Device · Class II · 2015-07-29 · Ekos
• The EkoSonic Endovascular System employs high frequency (2-2.5 MHz), low power (0.585 watt average power per transducer) ultrasound to faci…
  FDA Device · Class II · 2013-11-13 · Ekos
• EkoSonic MACH4 Endovascular Device (Catalog #500-55106, 500-55112
  FDA Device · Class II · 2012-07-25 · Ekos