—#116190

Product

Optetrak Logic Comprehensive Knee Prosthesis System, Proximal Tibial Spacer and screws, size 3.5, 8mm, Catalog # 02-012-42-3508.

FDA product code: JWH — Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Device class: Class 2
Medical specialty: Orthopedic
510(k) numbers: K071738
Affected lot / code info: Catalog # 02-012-42-3508 All lot numbers

Why it was recalled

A dimensional mismatch was identified which can potentially allow for interference between devices.

Root cause (FDA determination)

Device Design

Action the firm took

Exactech Inc. sent a *** Important *** Product Market Recall Notice dated January 30, 2013, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. 1. Customers were instructed to immediately cease distribution or use of these products. 2. Extend this information to your accounts that may have this product in their possession. 3. Verify if you have any of the subject Optetrak Logic Proxima Tibial Spacer (PTS) in the specified lots. Please complete the attached fax back form and return it to Exactech within the next 5 working days. Thank you for your prompt attention to this matter. For further questions please call (352) 377-1140.

Recalling firm

Firm: Exactech, Inc.
Address: 2320 NW 66th Ct, Gainesville, Florida 32653-1630

Distribution

Distribution pattern: Nationwide Distribution including the states of FL, AL, LA, PA, VA, IL, OH, NY, NC, KS, TN, NJ, CO, GA, CA, MD, MN, IN, & Puerto Rico.

Timeline

Recall initiated: 2013-02-01
Posted by FDA: 2013-03-15
Terminated: 2014-09-22
Status: —

Source: openFDA Device Recall endpoint. Recall record ID #116190. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.