FDA Medical Device Recalls (openFDA)
Abbott Spine: PathFinder Bone Drill-Awl-Tap, a part of the PathFinder spinal stablization system, Part Number 1156-50.
- Recall number
- Z-0004-2008
- Recalling firm
- Abbott Spine
- Product
- PathFinder Bone Drill-Awl-Tap, a part of the PathFinder spinal stablization system, Part Number 1156-50.
- Status
- Terminated
- Initiated
- 2007-07-18
- Posted
- 2007-10-02
- Terminated
- 2008-04-02
- Reason
- Tip of PathFinder surgical instrument broke during procedure.
- Root cause
- Device Design
- Action
- Firm notified sales representatives with an approved phone script on 7/18/2007.
- Quantity
- 11 units
- Distribution
- Nationwide.
- Lot, serial or model codes
- Part Numbers 1156-50, lot number 44QR.
- 510(k) numbers
- ["K030625"]
- PMA numbers
- not on file
- Product code
- NKB
- Firm FEI
- 3000718496
- Firm city
- Austin
- Firm state
- TX
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28