Zimmer, Inc.: Medical Device Recall in 2012 - (Recall #: Z-0553-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Persona, The Personalized Knee System, Tibial Sizing Plate, Cemented, Nonsterile, Size F Left; Size F Right This device is used with the Persona Knee System for patients with severe knee pain and disability due to: Rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis. o Collagen disorders, and/or avascular necrosis of the femoral condyle. o Post-traumatic loss of joint configuration, particularly when there is patellofemoral erosion, dysfunction or prior patellectomy. o Moderate valgus, varus, or flexion deformities

Product Classification:

Class II

Date Initiated: November 14, 2012

Date Posted: December 26, 2012

Recall Number: Z-0553-2013

Event ID: 63690

Reason for Recall:

All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed Natural Tibia implants, and associated tools including the Tibial Drill Guide, Broach, and Sizing Plate are being removed and replaced with enhanced products and instruments to reduce risks of tibial perforation which could result in tibial bone fracture due to the stress riser created by a perforation; tibial plate loosening

Status: Terminated

Product Quantity: 188

Code Information:

Part Number 42-5399-075-01(left) Lot 62052719, 62121529 Part Number 42-5399-075-02 (right), Lot 62072309, 62072566, 62121524

Distribution Pattern:

Worldwide Distribution - USA (nationwide) and internationally to Germany and Europe.

Voluntary or Mandated:

Voluntary: Firm initiated