Recall Z-0803-2018— Zimmer Biomet, Inc.
Class II · Terminated
Class II FDA medical device recall by Zimmer Biomet, Inc., initiated 2017-09-07, terminated 2018-08-23. FDA's recall record names no specific 510(k) clearance for this event. Product: The 2nd Assist Knee Positioner. Reason: Zimmer Biomet is conducting a medical device recall for the 2nd Assistant Knee Positioner due to the potential for the sterile packaging barrier to be breached during distribution..
- Recalling firm
- Zimmer Biomet, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-09-07
- Terminated
- 2018-08-23
- Firm location
- Warsaw, IN, United States
Product description
The 2nd Assist Knee Positioner
Reason for recall
Zimmer Biomet is conducting a medical device recall for the 2nd Assistant Knee Positioner due to the potential for the sterile packaging barrier to be breached during distribution.
Data sourced from openFDA. This site is unofficial and independent of the FDA.