Stelkast Co Stelkast Unicondylar Knee Femoral Component SC2462-1. Used for moderate joint impairment from painful arthritis (rheumatoid, osteo and/or post-traumatic; revision of failed unicompartmental knee implant or other procedure; and alternative to tibial osteotomy in patients with unicompartmental arthritis. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Stelkast Unicondylar Knee Femoral Component SC2462-1. Used for moderate joint impairment from painful arthritis (rheumatoid, osteo and/or post-traumatic; revision of failed unicompartmental knee implant or other procedure; and alternative to tibial osteotomy in patients with unicompartmental arthritis.
Brand
Stelkast Co
Lot Codes / Batch Numbers
Lot number 20210-100108
Products Sold
Lot number 20210-100108
Stelkast Co is recalling Stelkast Unicondylar Knee Femoral Component SC2462-1. Used for moderate joint impairment from painf due to incorrect size markings on component. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
incorrect size markings on component
Recommended Action
Per FDA guidance
The recalling firm telephoned the medical supply companies on 5/5-19/09 to inform them of the problem and the need to return the products. If there are questions regarding this issue, please call 1.888.273.1583.
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