Z-0371-06

Smith & Nephew Drill, 2.7mm for BioRaptor Suture Anchor (non-sterile) Reference Number: 7210430

Name: Z-0371-06 Smith & Nephew Drill, 2.7mm for BioRaptor Suture Anchor (non-sterile) Reference Number: 7210430
Creator: Smith & Nephew, Inc., Endoscopy Div.
Published: 2005-07-01
License: https://open.fda.gov/license/

Smith & Nephew, Inc. / initiated 2005-07-01 / Terminated

FDA source

Smith & Nephew, Inc., Endoscopy Div. began a recall of Smith & Nephew Drill, 2.7mm for BioRaptor Suture Anchor (non-sterile) Reference Number: 7210430 on 2005-07-01. The reason FDA records is "Drill does not contain laser etched depth marks to assure proper depth of inserted device". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0371-06
Status: Terminated
Initiated: 2005-07-01
Posted: 2006-01-11
Terminated: 2016-09-27
Recalling firm: Smith & Nephew, Inc.
Product: Smith & Nephew Drill, 2.7mm for BioRaptor Suture Anchor (non-sterile) Reference Number: 7210430
Product code: LXH Orthopedic Manual Surgical Instrument
Reason for recall: Drill does not contain laser etched depth marks to assure proper depth of inserted device
FDA root cause: Other
Action: Smith & Nephew notified accounts by Federal Express 07/01/2005 . Accounts are requested tor return units. Sales representatives notified by email.
Quantity in commerce: 4 units
Distribution: NC, PR
Product codes and lots: Lot Number: 50102446

Product code LXH

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)