Every recall we track for Stryker Spine — 10 in all — plus the complaints and injury reports the public filed about them.
Stryker Spine recalls Monterey AL Implant Inserter (22mm, Catalog 48019140) due to potential gold unlock button separation. Affected units have specific identifiers; contact for remedy.
Stryker Spine recalls Monterey AL Implant Inserter (18/20mm, Catalog 48019130) due to potential gold unlock button separation. Affected units have specific identifiers.
Stryker Spine recalls Monterey AL Implant Inserter (10/12mm, Catalog 48019100) due to potential gold unlock button separation. Affected units have specific identifiers; contact for remedy.
Stryker Spine recalls Monterey AL Implant Inserter (14/16mm, Catalog 48019120) due to potential gold unlock button separation. Affected units have specific identifiers; contact for remedy.
Stryker Spine recalls its AVS Anchor-C Cervical Cage System (revision 5) due to a labeling error in instructions for use. This correction affects U.S. and Canadian patients using the device for cervical fusion procedures.
Stryker Spine recalls LITe Decompression Snake Arm (REF 48080230) due to incorrect clamp component preventing attachment to arm post shaft. Affected units have UDI-DI GTIN 07613327263909, lot #227764.
Stryker recalls Cortoss Bone Augmentation Material 10cc Cartridges (Catalog 2101-0010) due to potential temperature excursion during distribution. Affected lots A1903054 and A1906006 may have been stored outside refrigeration for up to 12 hours.
Stryker recalls Cortoss Bone Augmentation Material 5cc Cartridges (Catalog 2101-0005) due to potential temperature excursion during distribution. Affected units may not meet refrigeration requirements.
Stryker Spine recalls specific lumbar intervertebral fusion instruments due to potential device failure during spinal surgery. Affected items include TL Inserter, Draw Rod, and Syringe Plunger components with UDI codes listed.
Stryker Spine recalls AVS Aria Cage (Catalog 48753212) due to anterior and posterior markers being on the wrong sides, potentially causing surgical errors. Affected patients should contact Stryker for guidance.
