Skip to content
Recall Observatory FDA recall evidence

Device product

Tibial Tray Nonporous A Size 2; Model # PN 162-1200-A; Material: Ti6Al4V.

Z-1903-2020

May 30, 2019

Class II

Product summary

Firm
Ortho Development Corporation
Event
Event 85157
Status
Ongoing
Classification
Class II
Quantity
27
Official record key
device-enforcement:Z-1903-2020

Official wording

Reason: The locking mechanism of the tibial tray exhibited a manufacturing defect in which a uniform ridge was cut along the inner wall of the "T" and "Y" junctions, which may cause resistance when the Tibial Insert was being assembled.

Code information: Lot Number: A200590

Distribution pattern: US: CA, FL, OH, PA, TX, and UT. OUS: Japan.

Derived failure modes

  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    manufacturing defect