Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-1963-2019)

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 Irrigation Tubing Assembly, Reference Number 423834 - 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-1963-2019

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: 211325 209586 210002 210488 210566 210848 210867 210972 211172 211237 212076 212488 212622 212928 212966 214005 214051 214118 214255 214499 214546 214669 214822 214995 215048 215329 215445 215524 215623 216489 216611 217370 217556 217761 217767 218667 219305 219661 219913 220935

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