Stryker Spine: Medical Device Recalls in 2021

According to to data from the FDA, there were 3 medical device recalls made by Stryker Spine in 2021. See the details of the recalls below.

You can see similar recalls for other firms.

• Tritanium X TL Instruments - intervertebral fusion device with bone graft, lumbar. Catalogs:TL Inserter (580220100), TL Draw Rod (580220101), Tube Set/Syringe Adapter Assembly (680220100), Syringe Plunger (680220102).
• Cortoss Bone Augmentation Material 10cc Cartridge, Catalog Number 2101-0010, GTIN 00808232000979
• Cortoss Bone Augmentation Material 5cc Cartridge, Catalog Number 2101-0005, GTIN 00808232000962