Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-1962-2019)

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:

Ultra-Drive Hose/Drape Assembly, Reference Number 423833 - Product Usage: Item used with the UltraDrive System to provide proper irrigation during the cutting and removal of bone and acrylic bone cement in orthopedic applications.

Product Classification:

Class II

Date Initiated: June 4, 2019

Date Posted: July 24, 2019

Recall Number: Z-1962-2019

Event ID: 83085

Reason for Recall:

The products do not have sufficient data to support the labeled shelf life of 10 years.

Status: Terminated

Product Quantity: 8478 total

Code Information:

Lot Numbers: 221437 211324 211638 212670 212877 213350 213612 214315 214545 214994 216550 216610 217760 217766 218921 219825

Distribution Pattern:

Worldwide distribution - US nationwide distribution and countries of Australia, Brazil, Canada, Chile, China, Columbia, Hong Kong, India, Japan, Malaysia, Netherlands, and Taiwan.

Voluntary or Mandated:

Voluntary: Firm initiated