FDA recall notice
Intra-Operative Positioning System Guidewire Recall: Centerline Biomedical Removes Certain…
FDA Recall Confirmed · IOPS Guidewire · posted Jun 13, 2025
Key facts
| Notice | Intra-Operative Positioning System Guidewire Recall: Centerline Biomedical Removes Certain IOPS Guidewires due to Delamination |
|---|---|
| Device type | IOPS Guidewire |
| Status | Recall Confirmed |
| Posted | Jun 13, 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: