Cranial Drill Urgent Recall Alert
Serious safety risksUrgent Class I Medical Device Recall
Integra LifeSciences has issued an urgent recall of specific Codman Disposable Perforators and Craniotomy Kits due to a serious manufacturing defect that may lead to device disassembly during neurosurgical procedures. The FDA has classified this as a Class I recall, the most serious type, due to the risk of severe injury or death.
Affected Products
- Codman Disposable Perforator 14 mm – UDI: 10381780513599
- Codman Craniotomy Kit (includes Perforator, Cranio-blade, Wire Pass Drill) – UDI: 10381780513629
Lot/Serial Numbers: Full List of Affected Lots
Reason for Recall
A faulty ultrasonic weld (known as a “proud weld”) on the device’s outer sleeve may cause the perforator to disassemble unexpectedly during use. In some cases, the device fails to disengage properly, putting patients at serious risk for:
- Brain tissue injury
- Bleeding or dural damage
- Extended surgery time
- Irreversible harm or even death
To date, 10 serious injuries have been reported—including devices lodged in the skull and fragments difficult to remove. No fatalities have been reported.
Recommended Actions for Users and Facilities
- Immediately stop using and quarantine all affected products.
- Review inventory against the provided lot numbers.
- Notify surgical and supply staff of the recall.
- Contact Integra for a Return Material Authorization (RMA) and return the product for credit.
Device Function
Codman Disposable Perforators are single-use neurosurgical tools designed to drill precise openings into the skull during craniotomy. They are engineered to disengage automatically after drilling to prevent over-penetration—but this defect undermines that safety feature.
Contact
For questions or to report issues, call Integra LifeSciences at 1-800-654-2873 or email FCA3@integralife.com.
Check the FDA recall web page for updates. The FDA is currently reviewing information about this potentially high-risk device issue and will keep the public informed as significant new information becomes available.
Now the Salmonella in Moringa Is Drug-Resistant
Now the Salmonella in Moringa Is Drug-Resistant. That Changes the Stakes. An MDP Consumer and Industry Brief Salmonella contamination is serious in any consumer product. But one of the most concerning developments in the latest moringa-related outbreak investigation...
Four Moringa-Linked Salmonella Events in Four Months
Four Moringa-Linked Salmonella Events in Four Months: The Timeline That Should Not Exist An MDP Consumer and Industry Brief A single recall can be dismissed as a one-time failure. Two recalls in the same ingredient category raise questions. But when moringa-based...
Rosabella Moringa Capsules Potential Salmonella Contamination
Rosabella Moringa Capsules Recalled Over Possible Salmonella Contamination Editor's Note: This February 13 recall is the latest moringa-root product recall, following the Sam's Super Greens recall in November, the Live it Up Super Greens recall on January 15, and the...