Smith & Nephew, Inc., Endoscopy Div. Smith & Nephew Drill, 2.7mm for BioRaptor Suture Anchor (non-sterile) Reference Number: 7210430 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Smith & Nephew Drill, 2.7mm for BioRaptor Suture Anchor (non-sterile) Reference Number: 7210430
Brand
Smith & Nephew, Inc., Endoscopy Div.
Lot Codes / Batch Numbers
Lot Number: 50102446
Products Sold
Lot Number: 50102446
Smith & Nephew, Inc., Endoscopy Div. is recalling Smith & Nephew Drill, 2.7mm for BioRaptor Suture Anchor (non-sterile) Reference Number: 7210430 due to Drill does not contain laser etched depth marks to assure proper depth of inserted device. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Drill does not contain laser etched depth marks to assure proper depth of inserted device
Recommended Action
Per FDA guidance
Smith & Nephew notified accounts by Federal Express 07/01/2005 . Accounts are requested tor return units. Sales representatives notified by email.
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
NC, PR
Page updated: Jan 10, 2026