Zimmer Biomet, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0304-2018)

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:

RED SEXP DSTL FEM 19CM RT ASSY, model # CP111817

Product Classification:

Class II

Date Initiated: June 5, 2017

Date Posted: January 10, 2018

Recall Number: Z-0304-2018

Event ID: 78167

Reason for Recall:

Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and actual product are correctly identified but the internal patient label could be incorrect.

Status: Terminated

Product Quantity: N/A

Code Information:

Lot Number: 856460

Distribution Pattern:

Nationwide in US; Internationally Argentina, Netherlands & Canada

Voluntary or Mandated:

Voluntary: Firm initiated