Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1962-2019 — 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.

U.S. FDA — Device Enforcement · United States · 2019-06-04 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1962-2019
Date of alert
2019-06-04
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer Biomet, Inc.
Product category
device
Product type
Devices
Reported risk: The products do not have sufficient data to support the labeled shelf life of 10 years.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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