Abbott Spine PathFinder Bone Drill-Awl-Tap, a part of the PathFinder spinal stablization system, Part Number 1156-50. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
PathFinder Bone Drill-Awl-Tap, a part of the PathFinder spinal stablization system, Part Number 1156-50.
Brand
Abbott Spine
Lot Codes / Batch Numbers
Part Numbers 1156-50, lot number 44QR.
Products Sold
Part Numbers 1156-50, lot number 44QR.
Abbott Spine is recalling PathFinder Bone Drill-Awl-Tap, a part of the PathFinder spinal stablization system, Part Number 1156 due to Tip of PathFinder surgical instrument broke during procedure.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Tip of PathFinder surgical instrument broke during procedure.
Recommended Action
Per FDA guidance
Firm notified sales representatives with an approved phone script on 7/18/2007.
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 noticePage updated: Jan 10, 2026