Defibtech, LLC: Medical Device Recall in 2020 - (Recall #: Z-2393-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

DDU-2400EN Lifeline PRO, UDI 00815098020270 - Product Usage: Automated External Defibrillators (AED) are indicated for use on victims of sudden cardiac arrest (SCA) who are: - unconscious and unresponsive, not breathing or not breathing normally.

Product Classification:

Class II

Date Initiated: April 27, 2020

Date Posted: June 24, 2020

Recall Number: Z-2393-2020

Event ID: 85702

Reason for Recall:

A component issue may cause the AED to abort a shock delivery or reset unexpectedly, which may cause an affected device to fail to delivery shock, and/or to fail to deliver shock in range.

Status: Terminated

Product Quantity: 860

Code Information:

Serial Number 400101322

Distribution Pattern:

Worldwide distribution - US Nationwide distribution and the countries of Australia, Canada, France, Malaysia, Mauritius, Netherlands, Thailand, United Arab Emirates.

Voluntary or Mandated:

Voluntary: Firm initiated