Exactech, Inc. 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
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
Exactech, Inc.
Lot Codes / Batch Numbers
Catalog no: 02-012-64-1812 Serial number: 6366405, 6367075, 6367076
Products Sold
Catalog no: 02-012-64-1812 Serial number: 6366405, 6367075, 6367076
Exactech, Inc. is recalling Truliant Splined Stem Extension, 18mm x 120mm - Product Usage: The devices are used in a cemented to due to These Truliant Splined Stem Extension, 18mm x 120mm were found to have a labeling error. The upper right corner of the label incorrectly identifies th. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026