Home / Recalls / Medical Devices
Zimmer Biomet, Inc. recalls Biomet 20mm Compress Device Short Anchor Plug With Drill Set / With Pin Inserter Ion Implant Item number: 178562 Pro
Recalled December 12, 2018 · FDA recall Z-0553-2019 · Zimmer Biomet
Hazard
Potential metal burrs in the holes of the device preventing the appropriate drill and transverse pins from being inserted · FDA Class II
Units
6 units
Sold at
US Nationwide Distribution in the states of IN, DC, MD
Description
Potential metal burrs in the holes of the device preventing the appropriate drill and transverse pins from being inserted
Product
Biomet 20mm Compress Device Short Anchor Plug With Drill Set / With Pin Inserter Ion Implant Item number: 178562 Product Usage: 1. Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. 2. Tumor resections. 3. Revision of previously failed total joint arthroplasty. 4. Trauma. The Compress¿ Segmental Femoral Replacement System (Short Spindle and Anchor Plug) components are intended for uncemented use only.
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →