TITAN SPINE, LLC Recalls

Overview of recall records associated with TITAN SPINE, LLC, including dates, categories and classifications where available.

2recall records

Aug 12, 2015latest record date

Apr 1, 2015earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceAug 12, 2015

Titan Spine Endoskeleton Locking Bone Screw Assembly, which is part of the Endoskeleton TCS recall — FDA Z-2327-2015

Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone Screw Assembly due to the locking bone screw collars not 'locking'.

Class IIFDA: TerminatedTITAN SPINE, LLC

Medical DeviceApr 1, 2015

TITAN SPINE Endo TCS Driver Straight Hexalobe #6 P/N 5210-1004, Non-Sterile, Manufactured by recall — FDA Z-1324-2015

The TCS Straight Hexlobular #6 Drivers (5210-1004) tip sheared off during use in procedures that involved patients with dense bones. As a result of this malfunction, Titan Spine, LLC is…

Class IIFDA: TerminatedTITAN SPINE, LLC

Understanding this recall history

This page summarizes recall records in which the official source identifies TITAN SPINE, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.