SpineFrontier, Inc.: Medical Device Recall in 2015 - (Recall #: Z-0977-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

lnline Persuader- PedFuse Pedicle Screw System; Part Number: 11-80164

Product Classification:

Class II

Date Initiated: December 19, 2014

Date Posted: January 21, 2015

Recall Number: Z-0977-2015

Event ID: 70065

Reason for Recall:

A crack may develop in the handle to the Inline Persuader, which may progress if the user continues to use the affected instrument.

Status: Terminated

Product Quantity: 4 devices

Code Information:

Lot/Serial Numbers: 06440-0000, 06441-0000, AG24

Distribution Pattern:

Nationwide Distribution including TX, OH, VA, and Washington, DC.

Voluntary or Mandated:

Voluntary: Firm initiated