Smith & Nephew Drill, 2.7mm for BioRaptor Suture Anchor (non-sterile) Reference Number: 7210430
FDA device recall Z-0371-06 · posted 2006-01-11 · Terminated
Recall details
- Recalling firm
- Smith & Nephew, Inc., Endoscopy Div.
- Reason for recall
- Drill does not contain laser etched depth marks to assure proper depth of inserted device
- Action taken
- Smith & Nephew notified accounts by Federal Express 07/01/2005 . Accounts are requested tor return units. Sales representatives notified by email.
- Root cause
- Other
- Status
- Terminated
- Product code
- LXH
- Quantity affected
- 4 units
- Distribution
- NC, PR
- Date initiated
- 2005-07-01
- Date posted
- 2006-01-11
- Date terminated
- 2016-09-27
- Location
- Mansfield, MA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.