Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Codman Cranial Hand Drill- Indicated when a craniotomy is required Recalled by Integra LifeSciences Corp. Due to Released with discoloration (rust) on the Drill Chuck...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Integra LifeSciences Corp. directly.
Affected Products
Codman Cranial Hand Drill- Indicated when a craniotomy is required for placement of an intracranial pressure (ICP) monitoring device and/or cerebrospinal fluid drainage device. Part Number: 82-6607
Quantity: 337 units
Why Was This Recalled?
Released with discoloration (rust) on the Drill Chuck and inner chuck of Codman Cranial Hand Drill may result in inflammation, local toxicity, systemic toxicity, sensitivity, revision surgery, procedural delay, inconvenience to user, and/or infection.
Where Was This Sold?
This product was distributed to 1 state: PA
About Integra LifeSciences Corp.
Integra LifeSciences Corp. has 216 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report