Cranial Drill Urgent Recall Alert

Serious safety risks

Urgent 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.

Recall Alert: AirLife/Vyaire Infant Breathing Systems

Class I Recall AirLife and manufacturer Vyaire are recalling specific Infant Heated Wire Circuits due to the risk that accessory adapters may disconnect during use, especially once the system reaches operating temperature. This could lead to serious injury or death,...

Avanos Recalls Ballard Closed Suction Systems

May result in non-sterile devices Avanos Medical, Inc. is recalling its Ballard Closed Suction Systems after identifying a failure in the sterilization process, which may result in non-sterile devices. Use of these products could lead to serious health risks,...

FDA Alert: Abiomed Impella Blood Pump Controller

Abiomed Impella blood pump controllers Controller May Fail to Detect Device Abiomed has issued an urgent safety notice for its Automated Impella Controller (AIC) due to a potentially serious issue where the system may fail to detect the Impella blood pump when...