FDA recall notice
Cranial Drill Recall: Integra LifeSciences Recalls Codman Disposable Perforators Due to…
FDA Recall Confirmed · Cranial Drill · posted Apr 23, 2026
Key facts
| Notice | Cranial Drill Recall: Integra LifeSciences Recalls Codman Disposable Perforators Due to Risk of Device Disassembly |
|---|---|
| Device type | Cranial Drill |
| Status | Recall Confirmed |
| Posted | Apr 23, 2026 |
| Notice on fda.gov | fda.gov |
At a glance
- Confirmed Recall confirmed
- Yes 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: