RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.): Medical Device Recall in 2020 - (Recall #: Z-0322-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Streamline OCT Navigated Instruments, Catalog numbers 26-DRILL-MDN 26-FTAP-30-MDN 26-FTAP-35-MDN 26-FTAP-40-MDN 26-FTAP-40-MDN 26-FTAP-45-MDN 26-S-FINDER-MDN Components of a surgical navigation device.

Product Classification:

Class II

Date Initiated: September 24, 2020

Date Posted: November 11, 2020

Recall Number: Z-0322-2021

Event ID: 86595

Reason for Recall:

System does not include a drill guide.

Status: Ongoing

Product Quantity: 76 units

Code Information:

Lots 370855 373847 373848 373849 377629 373850 373846

Distribution Pattern:

Distributed to one distributor in Michigan.

Voluntary or Mandated:

Voluntary: Firm initiated