FDA recall notice
Hemodialysis Bloodline Set Correction: B. Braun Medical Inc. Issues Correction for…
FDA Recall Confirmed · Bloodline Set · posted Apr 22, 2026
Key facts
| Notice | Hemodialysis Bloodline Set Correction: B. Braun Medical Inc. Issues Correction for Streamline Airless System Hemodialysis Bloodlines and B3 Low Volume Bloodlines |
|---|---|
| Device type | Bloodline Set |
| Status | Recall Confirmed |
| Posted | Apr 22, 2026 |
| Notice on fda.gov | fda.gov |
At a glance
- Confirmed Recall confirmed
- Yes Currently listed by the FDA
- 1–9 Recall events referenced
- 10–99 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: