PathFinder Bone Drill-Awl-Tap, a part of the PathFinder spinal stablization system, Part Number 1156-50.
FDA Recall Z-0004-2008 · Posted 2007-10-02
Recalling FirmAbbott Spine
Recall StatusTerminated
Product CodeNKB
Date Initiated2007-07-18
Date Terminated2008-04-02
Product Quantity11 units
Reason for Recall
Tip of PathFinder surgical instrument broke during procedure.
Firm Action
Firm notified sales representatives with an approved phone script on 7/18/2007.
Root Cause
Device Design
Distribution Pattern
Nationwide.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.