Exactech, Inc. recalls Optetrak Constrained Condylar Offset Screw, Size FF, Ref 208-04-74, Sterile, RX.

Recall date

September 19, 2017

Source

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

Recall number

Z-0150-2018

FDA classification

Class II

Brand / firm

Exactech, Inc.

Sold / distributed

Distribution was made to AL, FL, IN, ME, MN, NJ, NY, OH, OK, VA, and Puerto Rico. Foreign distribution was made to Argentina, Australia, Brazil, China, Colombia, France, India, Italy, Luxembourg, The Netherlands, Spain, Switzerland, Tunisia, and United Kingdom.

Why it was recalled

There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray.

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

What was recalled

Optetrak Constrained Condylar Offset Screw, Size FF, Ref 208-04-74, Sterile, RX.