Stryker Spine: Medical Device Recall in 2014 - (Recall #: Z-0803-2015)

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:

Specialty Audible Torque Wrench Mfg by: Stryker Spine, Catalog number IS3002XLP, Non-sterile. Used to final tighten to 12 Nm the blocker of the XIA 3, Hooks, Monoaxial Screws, Rod to Rod Connectors and Off-set connectors.

Product Classification:

Class II

Date Initiated: October 6, 2014

Date Posted: December 24, 2014

Recall Number: Z-0803-2015

Event ID: 69784

Reason for Recall:

Stryker has received a complaint from customers relating to a fracture during the use of the Specialty Audible Torque Wrench in surgery.

Status: Terminated

Product Quantity: 15 units

Code Information:

Lot number 4279

Distribution Pattern:

Distributed to GA, IN, MI, NJ, OH, PA, TX & VA.

Voluntary or Mandated:

Voluntary: Firm initiated