Class I — Serious Health Hazard

Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

CODMAN Disposable Perforator Recalled by Integra LifeSciences Corp. (NeuroSciences) Due to Inadequate weld that can potentially cause the product...

Date: April 11, 2025
Company: Integra LifeSciences Corp. (NeuroSciences)
Status: Ongoing
Source: FDA (Device)

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. (NeuroSciences) directly.

Affected Products

CODMAN Disposable Perforator, 14mm. Cranial perforator.

Quantity: 170,510 units

Why Was This Recalled?

Inadequate weld that can potentially cause the product to disassemble.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Integra LifeSciences Corp. (NeuroSciences)

Integra LifeSciences Corp. (NeuroSciences) has 23 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report