SpineFrontier, Inc.: Medical Device Recall in 2014 - (Recall #: Z-0624-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

PedFuse Bone Probe; Part: SI81008 spinal pedicle fixation.

Product Classification:

Class II

Date Initiated: September 11, 2013

Date Posted: January 15, 2014

Recall Number: Z-0624-2014

Event ID: 66273

Reason for Recall:

Bone Probes used to create a pathway in pedicle bone were manufactured and marked to incorrect specifications.

Status: Terminated

Product Quantity: 13 devices

Code Information:

Lot: 012212-001

Distribution Pattern:

US Distribution: including states of: TX and VA.

Voluntary or Mandated:

Voluntary: Firm initiated