Cranial Drill Recall: Integra Lifesciences Recalls Codman Disposable Perforators Due To Risk Of Device Disassembly
Recall Summary Integra LifeSciences is recalling certain Codman Disposable Perforators (surgical drilling devices used in brain surgery) because they may come apart during or after use. If the device disassembles, it could result in brain injury, bleeding, or extended surgical time. The recall affects medical facilities and surgeons who use these perforators in cranial procedures.
- Recalling firm
- Cranial Drill
- Product
- Codman Disposable Perforators
- Reason
- Certain Codman Disposable Perforators may disassemble during or after use, increasing the risk of brain injury, hemorrhage, or prolonged surgery.
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-MEDWATCH-RSS
- Recall date
- 2026-04-23
- Status
- Ongoing
Official recall notice from FDA-MEDWATCH-RSS
Recall details on Nibble Recalls: https://trynibble.app/recalls/782a542c-f71f-4b46-8317-eb1099846030