FDA Recall Open, Classified

DDU-100 Lifeline Automated External Defibrillator (AED)-Indicated for use on victims of sudden cardiac arrest

Recall: Z-1312-2023 · Initiated February 14, 2023

Recall

Recall Number
Z-1312-2023
Event Number
91799
Firm
Defibtech, LLC
FEI Number
3003521780
Product Code
MKJ
Status
Open, Classified
Root Cause
Device Design
Initiated
February 14, 2023
Posted
March 30, 2023
Address
741 Boston Post Rd, Suite 201, Guilford, CT, 06437-2714

Description

DDU-100 Lifeline Automated External Defibrillator (AED)-Indicated for use on victims of sudden cardiac arrest

Reason

A component of a sub-assembly used in the affected AEDs had not undergone durability and reliability testing, and if a malfunction occurs, therefore the device could fail to deliver therapy.

Action

Defibtech issued Urgent Medical Device Safety Removal User letter (FA2023-01) on 2/14/23 and 2/17/23 via email to Distributors and End-Users. Letter states reason for recall, health risk and action to take: 1. Confirm receipt of this notice by checking the Read receipt option in the email notification containing this communication. Additionally, complete, sign and return to [email protected] the attached Receipt Letter acknowledging that you have received this recall notification 2. Check the box label s 9-digit serial number of any units in your inventory against the serial numbers listed in the attachment 3. It is requested you quarantine the listed AEDs and Defibtech will contact you to arrange their return to Defibtech for screening 4. If you have further transferred the device to another entity or department, you must provide this notice to affected parties Please return any affected units as identified in the Attachment for replacement. Dedicated support for handling all aspects of the return of identified units will be provided by Defibtech. We will be contacting you shortly to help you with the process and answer any questions. If you have questions now, please feel free to contact us using the email address [email protected]. Defibtech Customer Support is available by calling 1-877-453-4507, 8:30 A.M. to 5:30 P.M. (Eastern), Monday - Friday. To assure that you have received notification of this safety issue and understand your obligation in notifying those in possession of the serial number(s) shipped to you or on your behalf of any required action, please sign and return this letter to [email protected].

Distribution

US Nationwide distribution.

Quantity

29 units