FDA recall notice
Angiographic Catheter Recall: Cook Removes Beacon Tip Angiographic Catheters due to Tip…
FDA Recall Confirmed · Angiographic Catheter · posted Jun 25, 2025
Key facts
| Notice | Angiographic Catheter Recall: Cook Removes Beacon Tip Angiographic Catheters due to Tip Separation |
|---|---|
| Device type | Angiographic Catheter |
| Status | Recall Confirmed |
| Posted | Jun 25, 2025 |
| Notice on fda.gov | fda.gov |
At a glance
- Confirmed Recall confirmed
- Yes Currently listed by the FDA
- None 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: