SpineFrontier, Inc.: Medical Device Recall in 2019 - (Recall #: Z-1973-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

A-CIFT SoloFuse Fixed Angle Driver, Model Number 13-32101-01 (Component Part Numbers 14-32107-01 and 14-32106)

Product Classification:

Class II

Date Initiated: June 13, 2019

Date Posted: July 24, 2019

Recall Number: Z-1973-2019

Event ID: 83166

Reason for Recall:

There is a potential for the driver to bind up when attempting to advance the intervertebral body fixation screw.

Status: Terminated

Product Quantity: 6

Code Information:

Lot EC20

Distribution Pattern:

The products were distributed to the following US states: AZ, MD, MO, and FL.

Voluntary or Mandated:

Voluntary: Firm initiated