BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall for Orthopaedic bone-nailing compression screw / Orthopaedic instrument connecting screw, Stryker

Product group Non-active implants
Reference 03201/10

Stryker Osteosynthesis has issued an information about a recall regarding the following product: Orthopaedic bone-nailing compression screw / Orthopaedic instrument connecting screw. The recall was a result of manufacturing error.

Recall for Orthopaedic bone-nailing compression screw / Orthopaedic instrument connecting screw, Stryker , Download_VeroeffentlichtAm_EN PDF, 27KB, File does not meet accessibility standards