DDU-2300 Lifeline/ReviveR View — Class II medical device recall Z-2392-2020
Terminated recall by Defibtech, LLC, reported 2020-06-24, distributed nationwide. A component issue may cause the AED to abort a shock delivery or reset unexpectedly, which may cause an affect
| Recall number | Z-2392-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Defibtech, LLC, Guilford, CT, United States |
| Recall initiated | 2020-04-27 |
| Classified | 2020-06-17 |
| Reported by FDA | 2020-06-24 |
| Terminated | 2021-01-08 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, CA, FR, MY, NL, TH |
| Quantity | 860 |
| UPC / GTIN / UDI-DI | 00815098020201, 00815098020225, 00815098020232 |
| Serial numbers | 400086354, 400086358, 400090005, 400091761, 400093477, 400093478, 400093479, 400093480, 400093481, 400093482, 400093483, 400093484, 400093485, 400093486, 400093487, 400093488, 400093489, 400093490, 400093491, 400093492, 400093493, 400093494, 400093495, 400093496, 400093497 and 475 more |
| Model numbers | CCD-A1006RX, CCD-A1013EN, CCD-A1015EN, DCF-A2310EN, DCF-A2310RX, DCF-A2313EN, DCF-C2310CA, DCF-C2310EN, DCF-E2310CA, DCF-E2310EN, DDU-A2300EN, DDU-C2300CA, DDU-C2300EN, DDU-E2300EN |
Product
DDU-2300 Lifeline/ReviveR View, Model Numbers DDU-C2300EN, DDU-C2300CA, DDU-A2300EN, DDU-E2300EN Catalog Numbers CCD-A1006RX CCD-A1013EN CCD-A1015EN DCF-A2310EN DCF-A2310RX DCF-A2313EN DCF-C2310CA DCF-C2310EN DCF-E2310CA DCF-E2310EN UDI 00815098020201, 00815098020225, 00815098020232 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.
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.
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-2392-2020. 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.