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# Class 1 Recall of Leonard Lang Defibrillation Electrodes
- URL: https://www.fdaweb.com/class-1-recall-of-leonard-lang-defibrillation-electrodes/
- Published: 2017-09-13T12:00:00.000Z
- Updated: 2026-09-14T22:49:32.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5139622

Leonhard Lang has recalled its Skintact multifunction defibrillation electrode models DF59N and DF59NC due to a connector compatibility issue with the Zoll Automatic External Defibrillator Plus. An FDA [recall notice](https://www.fda.gov/MedicalDevices/Safety/ListofRecalls/ucm575916.htm?ref=fdaweb.com) classifies it as Class 1 and says users may not be able to connect the electrodes to the defibrillator and this may result in a defibrillation shock being delayed or not delivered at all. Last month, the company sent a safety notification to all affected customers that instructed users to quarantine all affected products in stock and request replacement electrodes immediately.