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Terminated

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

FDA Recall Z-0371-06 · Posted 2006-01-11

Recalling FirmSmith & Nephew, Inc., Endoscopy Div.
Recall StatusTerminated
Product CodeLXH
Date Initiated2005-07-01
Date Terminated2016-09-27
Product Quantity4 units

Reason for Recall

Drill does not contain laser etched depth marks to assure proper depth of inserted device

Firm Action

Smith & Nephew notified accounts by Federal Express 07/01/2005 . Accounts are requested tor return units. Sales representatives notified by email.

Root Cause

Other

Distribution Pattern

NC, PR

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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