FDA Recall Open, Classified

The Graft Tube is an optional instrument which, as designed, can be filled with flowable graft material, then advanced through the Access Portal. A Push Rod is then used to facilitate the manual deployment of the graft material out of the Graft Tube and adjacent to where the implant is to be placed, as supported within the Surgical Technique Guide.

Recall: Z-0117-2025 · Initiated September 16, 2024

Recall

Recall Number
Z-0117-2025
Event Number
95341
Firm
Spineology, Inc.
FEI Number
3003179719
Product Code
LXH
Status
Open, Classified
Root Cause
Under Investigation by firm
Initiated
September 16, 2024
Posted
October 17, 2024
Address
7800 3rd St N, Ste 600, Saint Paul, MN, 55128-5455

Description

The Graft Tube is an optional instrument which, as designed, can be filled with flowable graft material, then advanced through the Access Portal. A Push Rod is then used to facilitate the manual deployment of the graft material out of the Graft Tube and adjacent to where the implant is to be placed, as supported within the Surgical Technique Guide.

Reason

Possible detachment of the Graft Tube shaft from the Graft Tube funnel head when it is not used as instructed by our surgical technique.

Action

Spineology began notification of medical institutions on 09/16/2024, direct sales representatives on 09/18/2024 and distributors on 09/19/2024 via letter. Instructions included to notify appropriate staff of the action and to complete and return the response form. Spineology will be performing a correction to update the surgical technique labeling and a removal will be conducted to replace current Graft Tubes within field inventory. Distributors were instructed to notify customers if further distributed.

Distribution

Pending

Quantity

190 units