Leonhard Lang Medizintechnik recalls

Leonhard Lang Medizintechnik appears in 4 official U.S. recall notices indexed by RecallRadar, most recently on 2017-09-20.

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

• Skintact Electrode for Defibrillation, Pacing, Monitoring, Cardioversion
  FDA Device · Class I · 2017-09-20 · Leonhard Lang Medizintechnik
• Skintact Electrodes for Defibrillation, DF29N. Product Usage: Multifunction electrode for external defibrillation, pacing, cardioversion, a…
  FDA Device · Class I · 2016-10-26 · Leonhard Lang Medizintechnik
• ECG Electrodes: 50007  Stablebase SBW55 50675  Stablebase SBW55-15 58051  Skintact W-60 50547  Stablebase SBT60 Only OUS: 50476 Skintac…
  FDA Device · Class II · 2015-11-25 · Leonhard Lang Medizintechnik
• Skintact ECG Electrode FS-50, Catalog no. 58028 , & Stable Base ECG Electrode SBT-60, Catalog no. 50547
  FDA Device · Class II · 2015-04-08 · Leonhard Lang Medizintechnik