PIONEER SURGICAL TECHNOLOGY, INC.: Medical Device Recall in 2014 - (Recall #: Z-2573-2014)

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:

STREAMLINE CT CERVICO-THORACIC SYSTEM; SET SCREW REF 26-SETSCREW NON-STERILE, SINGLE USE, RX ONLY

Product Classification:

Class II

Date Initiated: September 10, 2012

Date Posted: September 10, 2014

Recall Number: Z-2573-2014

Event ID: 69033

Reason for Recall:

Some set screw thread profiles were found not to be within specifications.

Status: Terminated

Product Quantity: 11 sets

Code Information:

Lot numbers: 104875, 104876, 104877, 104878, 104879, 104880, 104881 , 117030,117031 , 121947, 124260.

Distribution Pattern:

Distributed in the states of NC, NH, NY, CA, MI, IL, and FL.

Voluntary or Mandated:

Voluntary: Firm initiated