The Recall Desk

Manufacturer

TITAN SPINE, LLC

3 recalls in our database name TITAN SPINE, LLC as the manufacturing or recalling firm.

What the numbers show

Total
3
Critical
0
Severe
1
Most recent
2015-08-12

Of the 3 recalls from TITAN SPINE, LLC we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (33%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–3 of 3

  • HighFDA (Devices)·Z-2327-2015·2015-08-12

    Titan Spine Recalls Endoskeleton Locking Bone Screw Assemblies

    Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone Screw Assemblies because the locking collars are not locking.

    Product
    Titan Spine Endoskeleton Locking Bone Screw Assembly, which is part of the Endoskeleton TCS Interbody Fusion Device, spinal implant. Part Numbers / Product Description: 5302-3514 / 03.5 x 14mm Locking Screws; 5302-3516 / 03.5 x 16mm Locking Screws; 502-3518 / 03.5 x 18mm L
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-1324-2015·2015-04-01

    Titan Spine Recalls TCS Straight Hexalobe Drivers Due to Tip Shearing

    Titan Spine, LLC is recalling 26 Endo TCS Driver Straight Hexalobe #6 units because the tips sheared off during use in patients with dense bones.

    Product
    Endo TCS Driver Straight Hexalobe #6 P/N 5210-1004, Non-Sterile, Manufactured by Titan Spine, LLC. Endo TCS driver is one of the instruments within the surgical tray for use with the Interbody Fusion Device(IBD).
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Devices)·Z-0535-2013·2012-12-26

    Titan Spine Recalls Endoskeleton TA VBR Implants for Labeling Errors

    Titan Spine is recalling 92 Endoskeleton TA VBR implants because their labels contain incorrect indications for use.

    Product
    Titan Spine Endoskeleton TA Implant products. 2107-0118 18mm Standard Endoskeleton Implant VBR 2107-0120 20mm Standard Endoskeleton Implant VBR 2107-0218 18mm Large Endoskeleton Implant VBR 2107-0220 20mm Large Endoskeleton Implant VBR Endoskeleton TA VBR is intended
    Category
    Medical Device
    Distribution
    Distributed nationwide

About this company

Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.

TITAN SPINE, INC.

Source: Wikidata (Q140763679), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.