Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0735-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Maximum Variable Pitch Compression Screw Caddy, Reference Number 231201003 Product Usage: Intended to carry implants and instruments during regular inventory distribution and handling and sterilization in the hospitals

Product Classification:

Class II

Date Initiated: November 28, 2018

Date Posted: January 23, 2019

Recall Number: Z-0735-2019

Event ID: 81758

Reason for Recall:

There is a potential for silicone shedding during cleaning and sterilization.

Status: Terminated

Product Quantity: 971 in total

Code Information:

Lot Numbers 453392 453918 453919 469917 475577 481064 481065 486820 498695 506818 512867 512868

Distribution Pattern:

Worldwide Distribution - US Nationwide, The products were distributed to the following foreign countries: Australia, Chile, Netherlands.

Voluntary or Mandated:

Voluntary: Firm initiated