FDA recall notice
Early Alert: Catheter Introducer Issue from Abiomed and Oscor
FDA Early Alert - FDA collecting information · Catheter Introducer · posted Jun 18, 2026
Key facts
| Notice | Early Alert: Catheter Introducer Issue from Abiomed and Oscor |
|---|---|
| Device type | Catheter Introducer |
| Status | Early Alert - FDA collecting information |
| Posted | Jun 18, 2026 |
| Notice on fda.gov | fda.gov |
At a glance
- Early alert Recall confirmed
- No Currently listed by the FDA
- None 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: