PIONEER SURGICAL TECHNOLOGY, INC.: Medical Device Recall in 2014 - (Recall #: Z-2076-2014)

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:

Tritium Sternal Plate System, Screw, 02.7mm X 12mm, 12 Pack, Sterile. The Pioneer Surgical Cable Plate System is used in the stabilization and fixation of fractures of the anterior chest wall including Sternal fixation following Sternotomy and Sternal reconstructive surgical procedures. The screws are packaged as a 12 pack using a double tray packaging configuration.

Product Classification:

Class II

Date Initiated: June 11, 2014

Date Posted: July 23, 2014

Recall Number: Z-2076-2014

Event ID: 68619

Reason for Recall:

Lack of Sterility Assurance

Status: Terminated

Product Quantity: 5

Code Information:

Model: 86-27-12-S12 UDI Number: 00846468061463 LOT: 168952 Expiration:12/23/2018

Distribution Pattern:

US Nationwide Distribution in the states of TX and FL

Voluntary or Mandated:

Voluntary: Firm initiated