Defibtech DDP-2002: Pediatric Defibrillation Pads For use with AED… — Class II medical device recall Z-0505-2025
Ongoing recall by Defibtech, LLC, reported 2024-12-04. Within the Irish Market, that a Field Safety Notice is being issued due to a select number of authorized label
| Recall number | Z-0505-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Defibtech, LLC, Guilford, CT, United States |
| Recall initiated | 2024-10-14 |
| Classified | 2024-11-21 |
| Reported by FDA | 2024-12-04 |
| Countries outside the US | IE |
| Quantity | 22,294 total |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00815098020454, 10815098020451, 40815098020452 |
Product
Defibtech DDP-2002: Pediatric Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, Lifeline ECG, Lifeline View (DDU-2XXX Series -Indicated for use on victims of sudden cardiac arrest (SCA.)
Reason for recall
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0505-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.