Smith & Nephew Inc Tibial Base Plates Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Tibial Base Plates
Brand
Smith & Nephew Inc
Lot Codes / Batch Numbers
Tibial Base Plates 726100, 726101, 727100, 727101, 726202, 726203, 727202, 727203, 726304, 726305, 727304, 727305
Products Sold
Tibial Base Plates 726100, 726101, 727100, 727101, 726202, 726203, 727202, 727203, 726304, 726305, 727304, 727305
Smith & Nephew Inc is recalling Tibial Base Plates due to The firm received confirmed reports of Genesis Uni Articular Inserts not locking into tibial base plates intraoperatively.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The firm received confirmed reports of Genesis Uni Articular Inserts not locking into tibial base plates intraoperatively.
Recommended Action
Per FDA guidance
Recall notification was initiated by letter (Fed Ex) to domestic territory manager and sales representative and to international distributors (via email) on 06/21/2004 to request the return of any in stock product.
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