Recall Z-2198-2017— Zimmer Biomet, Inc.
Class II · Terminated
Class II FDA medical device recall by Zimmer Biomet, Inc., initiated 2017-05-08, terminated 2017-12-01. FDA's recall record names no specific 510(k) clearance for this event. Product: Reusable instruments in the Knee, Hip, Trauma, and Extremities segments.. Reason: Durability characteristics of reusable instruments were not established.
- Recalling firm
- Zimmer Biomet, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-05-08
- Terminated
- 2017-12-01
- Firm location
- Warsaw, IN, United States
Product description
Reusable instruments in the Knee, Hip, Trauma, and Extremities segments.
Reason for recall
Durability characteristics of reusable instruments were not established
Data sourced from openFDA. This site is unofficial and independent of the FDA.