Orthopedic Alliance LLC: Medical Device Recall in 2013 - (Recall #: Z-1380-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

UKNEE Patella,small 2401-1010 UKNEE Patella,medium 2401-1020 UKNEE Patella,large 2401-1030 UKNEE Patella,X-large 2401-1040 UKNEE Onset Patella, 3 pegs, x-small 2403-1010 UKNEE Onset Patella, 3 pegs, small 2403-1020 UKNEE Onset Patella, 3 pegs, medium 2403-1030 UKNEE Onset Patella, 3 pegs, large 2403-1040 UKNEE Onset Patella, 3 pegs,X-large 2403-1050 Variety of hip and knee implants and instruments, multiple uses.

Product Classification:

Class II

Date Initiated: February 20, 2013

Date Posted: June 5, 2013

Recall Number: Z-1380-2013

Event ID: 64588

Reason for Recall:

The recall of the Loaner Bin and Sterilization Trays for implants and instruments was initiated by Orthopedic Alliance because the directions for use and surgical techniques were not being provided to every physician and for every surgery.

Status: Terminated

Product Quantity: 57 units

Code Information:

Catalog No. 2401-1010 2401-1020 2401-1030 2401-1040 2403-1010 2403-1020 2403-1030 2403-1040 2403-1050

Distribution Pattern:

Nationwide Distribution including the states of CA, MD, TX, NV, and WI.

Voluntary or Mandated:

Voluntary: Firm initiated