FDA recall notice
Early Alert: Positive Pressure Breathing Device Issue from Baxter
FDA Early Alert - FDA collecting information · Positive Pressure Breathing Device · posted Jun 11, 2026
Key facts
| Notice | Early Alert: Positive Pressure Breathing Device Issue from Baxter |
|---|---|
| Device type | Positive Pressure Breathing Device |
| Status | Early Alert - FDA collecting information |
| Posted | Jun 11, 2026 |
| Notice on fda.gov | fda.gov |
At a glance
- Early alert Recall confirmed
- No 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: