Leonhard Lang Medizintechnik GmbH recalls

4 recalls on record · latest: August 8, 2017

Official U.S. recall history for Leonhard Lang Medizintechnik GmbH, compiled from official government records.

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Skintact Electrode for Defibrillation recalled over sterility concerns

August 8, 2017 · Medical device recalls High risk Certain lots of the defibrillation electrodes model DF59N and DF59NC may have a…

Skintact Electrodes for Defibrillation recalled over sterility concerns

September 1, 2016 · Medical device recalls High risk There is a risk that defibrillation electrodes model DF29N will be connected wi…

Leonhard Lang Medizintechnik GmbH recalls ECG Electrodes: 50007  Stablebase SBW55 50675  Stablebase SBW55-15 58051  Skintact W-60 50547  Stablebase SBT60 Onl…

November 2, 2015 · Medical device recalls Moderate risk There is a risk ECG electrodes of specific lots fail to transmit signals. There…

Leonhard Lang Medizintechnik GmbH recalls Skintact ECG Electrode FS-50, Catalog no. 58028 , & Stable Base ECG Electrode SBT-60, Catalog no. 50547. To acquire and…

February 24, 2015 · Medical device recalls Moderate risk The electrodes may fail to transmit signals.