FDA recall notice
Anesthesia Breathing Circuit Correction: Draeger, Inc. Updates Use Instructions for…
FDA Recall Confirmed · Anesthesia Breathing Circuit Kits · posted Jun 5, 2025
Key facts
| Notice | Anesthesia Breathing Circuit Correction: Draeger, Inc. Updates Use Instructions for VentStar Flex and Anesthesia Circuit Kits Due to Risk of Inadequate Ventilation from Cracked Hoses |
|---|---|
| Device type | Anesthesia Breathing Circuit Kits |
| Status | Recall Confirmed |
| Posted | Jun 5, 2025 |
| Notice on fda.gov | fda.gov |
At a glance
- Confirmed Recall confirmed
- Yes Currently listed by the FDA
- None Recall events referenced
- 1–9 UDI device identifiers named
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recall notices and early alerts
The FDA's Medical Device Recalls and Early Alerts list covers the most serious device recalls, plus early alerts about potentially high-risk device issues while the FDA is still collecting information. A notice is updated as the recall is confirmed or changes.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls and Early Alerts · Source date: