Recall issued by FDA for certain craniotomy kits

Jul 22, 2025 - 02:16 PM
FDA-device-recall

The Food and Drug Administration has identified a Class I recall of certain lots of  containing recalled Codman Disposable Perforators 14mm due to the potential of serious injury or death. The recall was issued due to an inadequate weld that may cause the perforator to come apart before, during or after use in a craniotomy procedure. The recall involves correcting the devices and does not call for them to be removed from where they are used or sold. 

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