FDA recall notice
Infusion Set Recall: BD and CareFusion 303, Inc. Remove BD Alaris Pump Infusion Sets
FDA Recall Confirmed · Infusion Set · posted Oct 5, 2026
Key facts
| Notice | Infusion Set Recall: BD and CareFusion 303, Inc. Remove BD Alaris Pump Infusion Sets |
|---|---|
| Device type | Infusion Set |
| Status | Recall Confirmed |
| Posted | Oct 5, 2026 |
| Notice on fda.gov | fda.gov |
At a glance
- Confirmed Recall confirmed
- Yes Currently listed by the FDA
- 1–9 Recall events referenced
- None 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: