Recall Z-2073-2017— Biomet Microfixation, LLC
Class II · Terminated
Class II FDA medical device recall by Biomet Microfixation, LLC, initiated 2017-04-11, terminated 2019-08-06. FDA's recall record names no specific 510(k) clearance for this event. Product: Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600. Reason: Part of the number on the tray lid differ from the part number on the base..
- Recalling firm
- Biomet Microfixation, LLC
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-04-11
- Terminated
- 2019-08-06
- Firm location
- Jacksonville, FL, United States
Product description
Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600
Reason for recall
Part of the number on the tray lid differ from the part number on the base.
Data sourced from openFDA. This site is unofficial and independent of the FDA.