Zimmer Biomet, Inc.: Medical Device Recall in 2018 - (Recall #: Z-1224-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

PERSONA¿ THE PERSONALIZED KNEE SYSTEM "PSN TIB STM 5 DEG SZ D R" indicated for patients with severe knee pain and disability due to: - Rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis.

Product Classification:

Class II

Date Initiated: December 12, 2017

Date Posted: April 4, 2018

Recall Number: Z-1224-2018

Event ID: 79394

Reason for Recall:

A complaint was received for Item 42-5320-067-02, lot 63236047. It was report that there was no set screw or taper plug included in the box. Complaint investigation confirmed that the entire lot of 63236047 was missing the set screw and taper plug.

Status: Terminated

Product Quantity: 3 units

Code Information:

Item# 42-5320-067-02 Lot # 63236047

Distribution Pattern:

Non-USA Customer

Voluntary or Mandated:

Voluntary: Firm initiated