Zimmer Biomet, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0992-2018)

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:

DELTA CER FEM HD 32/0MM T1 Product Usage: For use in hip arthroplasty

Product Classification:

Class II

Date Initiated: June 30, 2017

Date Posted: March 21, 2018

Recall Number: Z-0992-2018

Event ID: 79242

Reason for Recall:

Product may contain the presence of melted sterile packaging upon opening.

Status: Terminated

Product Quantity: 30

Code Information:

part number: 650-1162 lot number: 2016030466

Distribution Pattern:

US in the state of Texas

Voluntary or Mandated:

Voluntary: Firm initiated