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Medical Procedure Kits Correction: Medline Industries, LP Issues Correction for Medline Craniotomy Kits Containing Codman Disposable Perforators Due to Risk for Device Disassembly

Medline Industries, LP is correcting certain lots of their Craniotomy Kits containing recalled Codman Disposable Perforators 14mm. Integra LifeSciences is recalling the perforators due to an inadequate weld that may cause the perforator to come apart before, during or after use in a craniotomy procedure.  

This recall involves correcting certain devices and does not involve removing them from where they are used or sold. The FDA has identified this recall as a Class I recall, the most serious type. This device may cause serious injury or death if you continue to use it without correction. 

Questions?

Customers in the U.S. with questions about this recall should contact Medline’s Recall Department at 866-359-1704 or recalls@medline.com.