RecallRadar

FDA Device recall Z-2792-2016

Femoral Nail, A/R T2 Femur 011x280 mm T2 Femoral Nailing System is one of the first femoral nailing systems to offer an option for either a…

On 2016-09-21 the FDA classified a Class II recall of Femoral Nail, A/R T2 Femur 011x280 mm T2 Femoral Nailing System is one of the first femoral nailing systems to offer an option for either a… by Stryker Howmedica Osteonics, citing stryker discovered that a Tibial Nail and femoral Nail were incorrectly labeled and distributed to the field.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2792-2016
ClassificationClass II
Statusterminated
Initiated2016-06-30
Published2016-09-21
Last updated2026-09-13 11:54 UTC
CompanyStryker Howmedica Osteonics
DistributionCA

Product

Femoral Nail, A/R T2 Femur 011x280 mm T2 Femoral Nailing System is one of the first femoral nailing systems to offer an option for either an antegrade or a retrograde approach to repair fractures of the femur. (1) Open and closed femoral fractures, (2) Pseudoarthrosis and correction, (3) osteotomy, (4) Pathologic fractures, impending pathologic fractures, and tumor resections, (5) Supracondylar fractures, including those with intra-articular extension, (6) Ipsilateral femur fractures, (7) Fractures proximal to a total knee arthroplasty, (8) Fractures distal to a hip joint and (9) Non-unions and malunions

Reason

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

Identifiers

code_infoCatalog number 18251032S and Lot Code K288335

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2792-2016%22

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