Smith & Nephew Inc Genesis II, Cruciate Retaining, Oxinium, Femoral component, Size 5 right, Part No. 71420152 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Genesis II, Cruciate Retaining, Oxinium, Femoral component, Size 5 right, Part No. 71420152
Brand
Smith & Nephew Inc
Lot Codes / Batch Numbers
05LM01939
Products Sold
05LM01939
Smith & Nephew Inc is recalling Genesis II, Cruciate Retaining, Oxinium, Femoral component, Size 5 right, Part No. 71420152 due to Mispackaging-A size 5 femoral component, left, box had a size 5 right component in the box.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Mispackaging-A size 5 femoral component, left, box had a size 5 right component in the box.
Recommended Action
Per FDA guidance
All consignees were notified of the potential swap on 4/11/2006 via phone. The firm followed with a recall notice dated 05/18/2006.
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 noticeDistribution
As reported by FDA
IN, LA, NC
Page updated: Jan 10, 2026