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Leonhard Lang Medizintechnik Recalls
4 recalls on record · April 8, 2015 to September 20, 2017 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
September 20, 2017Medical DevicesFDA
Leonhard Lang Medizintechnik GmbH recalls Skintact Electrode for Defibrillation, Pacing, Monitoring, Cardioversion. Product Usage: Multifunction electrode for
Hazard: Certain lots of the defibrillation electrodes model DF59N and DF59NC may have a delay in connecting or not connect at all with the defibrillator ZOLL AED PLUS. This may cause a situation in which a patient, who is in a life threatening condition and requires a defibrillation shock, cannot be treated in good time.
October 26, 2016Medical DevicesFDA
Leonhard Lang Medizintechnik GmbH recalls Skintact Electrodes for Defibrillation, DF29N. Product Usage: Multifunction electrode for external defibrillation, p
Hazard: There is a risk that defibrillation electrodes model DF29N will be connected with the defibrillator Welch Allyn AED 10 only with delay or not at all. This may cause a situation in which a patient, who is in a life threatening condition and requires a defibrillation shock, cannot be treated in good time.
November 25, 2015Medical DevicesFDA
Leonhard Lang Medizintechnik GmbH recalls ECG Electrodes: 50007 Stablebase SBW55 50675 Stablebase SBW55-15 58051 Skintact W-60 50547 Stablebase SBT6
Hazard: There is a risk ECG electrodes of specific lots fail to transmit signals. There is a risk that the affected electrodes will transmit a poor signal or no signal at all before reaching the indicated expiration date.
April 8, 2015Medical DevicesFDA
Leonhard Lang Medizintechnik GmbH recalls Skintact ECG Electrode FS-50, Catalog no. 58028 , & Stable Base ECG Electrode SBT-60, Catalog no. 50547. To acqui
Hazard: The electrodes may fail to transmit signals.