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.

MicroMyst Applicator Recalled by Integra LifeSciences Corp. (NeuroSciences) Due to Lack of sterility assurance.

Date: May 23, 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

MicroMyst Applicator, Box of 5. Consisting of a multilumen applicator and filtered line for use with the Integra Flow Source for the controlled application of two liquids.

Quantity: 4,882 units

Why Was This Recalled?

Lack of sterility assurance.

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