Esaote S P A recalls

Esaote S P A appears in 9 official U.S. recall notices indexed by RecallRadar, most recently on 2026-03-11.

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

• Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038
  FDA Device · Class II · 2026-03-11 · Esaote S P A
• AC/DC POWER SUPPLY for 7400, Part Number 151004301, XP Power Model Number AHM180PS19-XE1057, AC/DC Adapter associated with the following po…
  FDA Device · Class II · 2020-10-07 · Esaote S P A
• AC/DC POWER SUPPLY for 7400, Part Number 151004300, XP Power Model Number AHM180PS19-XE0338, AC/DC Adapter associated with the following po…
  FDA Device · Class II · 2020-10-07 · Esaote S P A
• MyLab Alpha, Model 7400
  FDA Device · Class II · 2018-10-31 · Esaote S P A
• MyLab Gamma, Model 7410
  FDA Device · Class II · 2018-10-31 · Esaote S P A
• MyLab Seven, Model 6400
  FDA Device · Class II · 2018-10-31 · Esaote S P A
• MyLab Ultrasound System
  FDA Device · Class II · 2018-03-28 · Esaote S P A
• MyLab Ultrasound System
  FDA Device · Class II · 2018-03-28 · Esaote S P A
• Magnetic Resonance System G-scan Brio (Part Number /Model No.101002000)
  FDA Device · Class II · 2016-07-13 · Esaote S P A