Integra LifeSciences Corp. (NeuroSciences): Device Recall

Recall #Z-1961-2025 · 05/23/2025

Class I: Dangerous

Recall Details

Recall Number
Z-1961-2025
Classification
Class I
Product Type
Device
Recalling Firm
Integra LifeSciences Corp. (NeuroSciences)
Status
Ongoing
Date Initiated
05/23/2025
Location
Princeton, NJ, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
4,882 units

Reason for Recall

Lack of sterility assurance.

Product Description

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.

Distribution Pattern

Worldwide distribution - US Nationwide and the countries of Taiwan (Province of China), Viet Nam, Brazil, Trinidad and Tobago, El Salvador, South Korea, Peru, Canada, Australia, New Zealand, Belgium, France, Germany, Ireland, Israel, Italy, Kenya, Slovenia, South Africa, Spain, Sweden, Switzerland and United Kingdom.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.