Zimmer Biomet, Inc. 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. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
Zimmer Biomet, Inc.
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
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
Zimmer Biomet, Inc. is recalling Ultra-Drive Irrigation Tubing Assembly, Reference Number 423834 - Product Usage: Item used with the due to The products do not have sufficient data to support the labeled shelf life of 10 years.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The products do not have sufficient data to support the labeled shelf life of 10 years.
Recommended Action
Per FDA guidance
Urgent Medical Device Recall notification letters dated 6/4/19 were sent to customers.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026