Alaris EtCO2 Module Model 8300 — Class I medical device recall Z-2721-2020
Terminated recall by CareFusion 303, Inc., reported 2020-08-12, distributed nationwide. Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may lead to interruption of communicat
| Recall number | Z-2721-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CareFusion 303, Inc., San Diego, CA, United States |
| Recall initiated | 2020-06-30 |
| Classified | 2020-08-06 |
| Reported by FDA | 2020-08-12 |
| Terminated | 2024-04-22 |
| Distributed | Nationwide (US) |
| Quantity | 38,982 |
| Model numbers | 8300 |
Product
Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system
Reason for recall
Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may lead to interruption of communication or power between PC Unit and modules, which may result in an infusion that stops with a CHANNEL DISCONNECTED message, and an audio/visual alarm on the PC Unit and an interruption of therapy or monitoring.
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-2721-2020. 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.