Zimmer, Inc.: Medical Device Recall in 2012 - (Recall #: Z-0386-2013)

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:

Trilogy II Constrained Liner The Trilogy Longevity Constrained Liner serves as the articular surface for a femoral head in total hip arthroplasty.

Product Classification:

Class II

Date Initiated: August 27, 2012

Date Posted: November 28, 2012

Recall Number: Z-0386-2013

Event ID: 63126

Reason for Recall:

Trilogy Longevity Constrained Liner devices were packaged in incorrect cartons. The product is packaged in the incorrect carton. Product labels and patient labels are correct, matching the product inside the carton.

Status: Terminated

Product Quantity: 1

Code Information:

Item 00-6334-062-36, Lot 62023769

Distribution Pattern:

USA (nationwide) including the states of Ohio, Carolinas and New England.

Voluntary or Mandated:

Voluntary: Firm initiated