FDA Recall Open, Classified

Truliant Splined Stem Extension, 18mm x 120mm - Product Usage: The devices are used in a cemented total knee prosthesis system, which provides femoral components, tibial inserts, stems, augments, and surgical instrumentation for use in primary and revision total knee arthroplasty.

Recall: Z-1364-2020 · Initiated January 27, 2020

Recall

Recall Number
Z-1364-2020
Event Number
84961
Firm
Exactech, Inc.
FEI Number
1038671
Product Code
JWH
Status
Open, Classified
Root Cause
Labeling mix-ups
Initiated
January 27, 2020
Address
2320 NW 66th Ct, Gainesville, FL, 32653-1630

Description

Truliant Splined Stem Extension, 18mm x 120mm - Product Usage: The devices are used in a cemented total knee prosthesis system, which provides femoral components, tibial inserts, stems, augments, and surgical instrumentation for use in primary and revision total knee arthroplasty.

Reason

These Truliant Splined Stem Extension, 18mm x 120mm were found to have a labeling error. The upper right corner of the label incorrectly identifies the implant size as 17mm x 80mm when the implant size is 18mm x 120mm.

Action

Exactech distributed the recall notice to the consignees in possession of affected inventory by electronic mail on 7 January 2020. In order to comply with the notice, consignees have been instructed to: "Immediately cease distribution or use of this product. "Extend the information to their accounts that may have this product in their possession. "Identify and quarantine any of the subject devices in their inventory "Complete and return the attached Recall Acknowledgment Form and Recall Inventory Response Form to Exactech.

Distribution

US Nationwide distribution in the states of AZ, CO and FL.

Quantity

4 units