Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Skintact Electrode for Defibrillation Recalled by Leonhard Lang Medizintechnik GmbH Due to Certain lots of the defibrillation electrodes model DF59N...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Leonhard Lang Medizintechnik GmbH directly.
Affected Products
Skintact Electrode for Defibrillation, Pacing, Monitoring, Cardioversion. Product Usage: Multifunction electrode for external defibrillation, pacing, cardioversion, and monitoring. The device is non-sterile and for single use only. Used with automated external defibrillators
Quantity: 8,249 units total
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 2 states: FL, TX
About Leonhard Lang Medizintechnik GmbH
Leonhard Lang Medizintechnik GmbH has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report