Genesis II, Cruciate Retaining, Oxinium, Femoral component, Size 5 right, Part No. 71420152
FDA device recall Z-1157-06 · posted 2006-06-17 · Terminated
Recall details
- Recalling firm
- Smith & Nephew Inc
- Reason for recall
- Mispackaging-A size 5 femoral component, left, box had a size 5 right component in the box.
- Action taken
- 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.
- Root cause
- Other
- Status
- Terminated
- Product code
- HSX
- Quantity affected
- 3 units
- Distribution
- Worldwide-including states of LA, NC, IN, and countries of France, and Turkey
- Date initiated
- 2006-04-12
- Date posted
- 2006-06-17
- Date terminated
- 2007-04-11
- Location
- Memphis, TN
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.