Flow-i C20 Anesthesia System — Class II medical device recall Z-0987-2024
Ongoing recall by Getinge Usa Sales Inc, reported 2024-02-14, distributed nationwide. Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remot
| Recall number | Z-0987-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Getinge Usa Sales Inc, Wayne, NJ, United States |
| Recall initiated | 2023-12-11 |
| Classified | 2024-02-06 |
| Reported by FDA | 2024-02-14 |
| Distributed | Nationwide (US) |
| Quantity | 128 |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 07325710001349 |
| Serial numbers | 1202, 1224, 1281, 1282, 1545, 1546, 1651, 1657, 1786, 1787, 1860, 1861, 2023, 2024, 2095, 2186, 2557, 2558, 2559, 2560, 2613, 2714, 2716, 2719, 2720 and 104 more |
| Model numbers | 6677200 |
Product
Flow-i C20 Anesthesia System, model 6677200
Reason for recall
Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous situation.
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-0987-2024. 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.