Integra LifeSciences Corp. (NeuroSciences): Device Recall

Recall #Z-1716-2025 · 04/11/2025

Class I: Dangerous

Recall Details

Recall Number
Z-1716-2025
Classification
Class I
Product Type
Device
Recalling Firm
Integra LifeSciences Corp. (NeuroSciences)
Status
Ongoing
Date Initiated
04/11/2025
Location
Princeton, NJ, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
170,510 units

Reason for Recall

Inadequate weld that can potentially cause the product to disassemble.

Product Description

CODMAN Disposable Perforator, 14mm. Cranial perforator.

Distribution Pattern

Worldwide distribution - US Nationwide including Puerto Rico and the countries of Argentina, Australia, Austria, Bahamas, Barbados, Belgium, Brazil, Canada, Chile, Colombia, Cyprus, Czechia, Dominican Republic, Ecuador, El Salvador, France, French Guiana, Germany, Ghana, Greece, Hong Kong, India, Ireland, Israel, Italy, Japan, Jordan, Kenya, Korea (the Republic of), Lebanon, Lithuania, Malaysia, Morocco, Nepal, Netherlands, New Zealand, Pakistan, Poland, Portugal, Qatar, Saudi Arabia, Singapore, Slovenia, South Africa, Spain, Sri Lanka, Sweden, Switzerland, Taiwan, Thailand, Trinidad and Tobago, Tunisia, Turkey, United Arab Emirates, 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.