DePuy Orthopaedics, Inc.: Medical Device Recall in 2018 - (Recall #: Z-2949-2018)

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:

P.F.C. SIGMA Revision Knee System Distal Augment, Model Number 960830

Product Classification:

Class II

Date Initiated: July 18, 2018

Date Posted: September 5, 2018

Recall Number: Z-2949-2018

Event ID: 80666

Reason for Recall:

This unit may be missing the screw/collet Assembly

Status: Terminated

Product Quantity: 1

Code Information:

Lot: C2KJ24, GTIN: 10603295234135

Distribution Pattern:

The devices were not distributed in the United States. The devices were distributed to the following foreign countries: Great Britain.

Voluntary or Mandated:

Voluntary: Firm initiated