Synthes (USA) Products LLC recalls Synthes VA Implant Rack for the Compact Distal Radius System Tray/Surgical/Instrument

Recall date

November 29, 2016

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0867-2017

FDA classification

Class II

Brand / firm

Synthes (USA) Products LLC

Sold / distributed

Nationwide Distribution

Why it was recalled

The screw rack plate was assembled incorrectly which could cause the screws in the screw rack to sit low and touch the surface beneath the screw rack.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Synthes VA Implant Rack for the Compact Distal Radius System Tray/Surgical/Instrument