Lma North America recalls

Lma North America appears in 1 official U.S. recall notice indexed by RecallRadar, most recently on 2012-07-25.

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

• LMA Esophageal Intubation Detector (EID), Catalog Number EID100 The device is used to assist verification of placement of the endotracheal…
  FDA Device · Class II · 2012-07-25 · Lma North America