FDA Device recall Z-0988-2024
Flow-i C30 Anesthesia System, model 6677300
- FDA Device
- Class II
- ongoing
- Published 2024-02-14
On 2024-02-14 the FDA classified a Class II recall of Flow-i C30 Anesthesia System, model 6677300 by Getinge Usa Sales, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0988-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-12-11 |
| Published | 2024-02-14 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Getinge Usa Sales |
| Distribution | US |
Product
Flow-i C30 Anesthesia System, model 6677300
Reason
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.
Identifiers
| code_info | UDI-DI: 07325710001363, serial numbers (US): 1058, 1060, 1167, 1201. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0988-2024%22
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