BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall for "Cancellous Bone Screws and Gap Plate Screws", Stryker

Product group Non-active implants
Reference 02438/09

Stryker GmbH & Co. KG has initiated a lot specific product recall of its Cancellous Bone Screws and Gap Plate Screws. The material used for their manufacture does not comply with the metallurgical requirements outlined in ASTM Standards for titanium surgical implants.

Recall for "Cancellous Bone Screws and Gap Plate Screws", Stryker , Download_VeroeffentlichtAm_EN PDF, 240KB, File does not meet accessibility standards