Biomet, Inc. recalls Compress Device Segmental Anchor Plug, 10 MM-For Correction
Recalled Product
Compress Device Segmental Anchor Plug, 10 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178400
Hazard / Issue
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Issued by
FDA
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