Z-2073-2017 Class II Terminated
FDA device recall Z-2073-2017 was initiated by Biomet Microfixation, LLC on April 11, 2017 and is designated Class II. Reason for recall: Part of the number on the tray lid differ from the part number on the base. The recall status is terminated (terminated August 6, 2019). Affected quantity: 33 units.
Recall Details
- Product Type
- Devices
- Report Date
- May 24, 2017
- Initiation Date
- April 11, 2017
- Termination Date
- August 6, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 33 units
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.
Distribution Pattern
AL, MO and UT Canada, Australia, Netherlands, and Egypt
Code Information
Part Number 46-1610 // Lot Number 709730 Part Number 46-1610 // Lot Number 709740 Part Number 46-1620 // Lot Number 709710 Part Number 46-1620 // Lot Number 709720