Medical DeviceMay 14, 2025
Integra LifeSciences CODMAN Disposable Perforator, 14mm recall — FDA Z-1716-2025
Inadequate weld that can potentially cause the product to disassemble.
Class IFDA: OngoingIntegra LifeSciences Corp. (NeuroSciences)
Recall history in this database
Classification mix: Class II: 17, Class I: 8.
Understanding this recall history
This page summarizes recall records in which the official source identifies Integra LifeSciences Corp. (NeuroSciences) as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.