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Integra LifeSciences Corp. (NeuroSciences) recalls CODMAN Disposable Perforator, 14mm. Cranial perforator.
Recalled May 14, 2025 · FDA recall Z-1716-2025 · Integra LifeSciences Corp. (NeuroSciences)
Hazard
Inadequate weld that can potentially cause the product to disassemble. · FDA Class I
Units
170,510 units
Sold at
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.
Description
Inadequate weld that can potentially cause the product to disassemble.
Product
CODMAN Disposable Perforator, 14mm. Cranial perforator.
Manufacturer(s)
Integra LifeSciences Corp. (NeuroSciences)
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →