Stryker Howmedica Osteonics Corp.: Medical Device Recall in 2016 - (Recall #: Z-2791-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Supracondylar Nail T2 SCN 09x300 mm T2 Supracondylar Nail System is intended to provide strong and stable internal fixation with minimal soft tissue irritation of the distal femur. (1( Open and closed femoral fractures, (2) Pseudoarthrosis and correction osteotomy, (3) Pathologic fractures, impending pathologic fractures, and tumor resections, (4) Supracondylar fractures, including those with intra-articular extension, (5) Fractures distal to a Total Hip Prosthesis and (6) Non-unions and malunions

Product Classification:

Class II

Date Initiated: June 30, 2016

Date Posted: September 21, 2016

Recall Number: Z-2791-2016

Event ID: 74727

Reason for Recall:

Stryker discovered that a Tibial Nail and femoral Nail were incorrectly labeled and distributed to the field.

Status: Terminated

Product Quantity: 1 unit in total

Code Information:

Catalog number 18220930S and Lot Code K836729

Distribution Pattern:

US distribution to state of: CA.

Voluntary or Mandated:

Voluntary: Firm initiated