FDA recall notice
Blood Products Administration Set Recall: Fresenius Kabi Removes Large Volume Pump Blood…
FDA Recall Confirmed · Blood Products Administration Set · posted Jun 17, 2025
Key facts
| Notice | Blood Products Administration Set Recall: Fresenius Kabi Removes Large Volume Pump Blood Products Administration Set due to Incorrect Assembly |
|---|---|
| Device type | Blood Products Administration Set |
| Status | Recall Confirmed |
| Posted | Jun 17, 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: