Biomet Microfixation, LLC recalls Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600

Recalled May 24, 2017 · FDA recall Z-2073-2017 · Biomet Microfixation

Hazard

Part of the number on the tray lid differ from the part number on the base. · FDA Class II

Units

33 units

Sold at

AL, MO and UT Canada, Australia, Netherlands, and Egypt

Description

Part of the number on the tray lid differ from the part number on the base.

Product

Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600

Manufacturer(s)

Biomet Microfixation, LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →