BfArM - Federal Institute for Drugs and Medical Devices

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Product group Non-active implants
Reference 01262/09

OIC Cage: The company Stryker has informed about a lot recall of this spine implant. The action was initiated because of a labelling error in such a way that the product was marked with ‚PEEK-Ta’ instead of ‚PEEK-Ti’. Advisory Notice is only available in German language.

Recall for OIC Cage, Stryker , Download_VeroeffentlichtAm_EN PDF, 104KB, File does not meet accessibility standards