Zimmer Biomet, Inc.: Medical Device Recall in 2020 - (Recall #: Z-1000-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Coonrad/Morrey Total Elbow Humeral Assembly, Extra Small, 4-inch Length. Model No. 32-8105-027-04. UDI (01)00889024274006 (17)241031(10)64481139 The device is a Humeral component; elbow joint metal/polymer constrained cemented prosthesis.

Product Classification:

Class II

Date Initiated: December 12, 2019

Date Posted: February 12, 2020

Recall Number: Z-1000-2020

Event ID: 84636

Reason for Recall:

The lot contained two outer pins instead of one outer and one inner pin.

Status: Terminated

Product Quantity: 3

Code Information:

Lot 64481139

Distribution Pattern:

Distributed to accounts in California and Ohio.

Voluntary or Mandated:

Voluntary: Firm initiated