Defibtech, LLC 2024-12-04 Health serious FDA
Health · FDA · Recall #FDA-Z-0504-2025
Defibtech DDP-2001: Adult Defibrillation Pads For use with AED Models: Lifeline View… Recall
Issued December 4, 2024 · Defibtech, LLC
In December 2024, Defibtech, LLC recalled the Defibtech DDP-2001: Adult Defibrillation Pads For use with AED Models: Lifeline View…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Within the Irish Market, that a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech AED Pads, which have had the authorized label removed and an unauthorized label applied, could potentially lead to expired Defibtech AED Pads appearing as though they are within the acceptable shelf life.there is a possibility of hydrogel drying, which may result in poor electrical connection to the patient, which can reduce the energy delivered to the patient
What you should do
- 1 Stop using Defibtech DDP-2001: Adult Defibrillation Pads For use with AED Models: Lifeline View… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Defibtech, LLC to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Defibtech, LLC
- Category
- Health
- Recall date
- December 4, 2024
- Units affected
- Not reported
- Sold at
- Ireland
- Recall number
- FDA-Z-0504-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Defibtech, LLC has 2 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.