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.
Other Recalls by Integra LifeSciences Corp. (NeuroSciences)
- Class II: Risk 12/12/2025
- Class II: Risk 12/12/2025
- Class II: Risk 10/03/2025
- Class I: Dangerous 09/26/2025
- Class I: Dangerous 09/26/2025
View all recalls by Integra LifeSciences Corp. (NeuroSciences) →
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.