Medical Device Recall: Z-0004-2008

FDA Recalls dataset · Firm: Abbott Spine · Status: Terminated

Recall Action Class: N/A Date Initiated: 2007-07-18 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0004-2008.

Recall Res Number
Z-0004-2008
Recalling Firm / Manufacturer
FEI Number
3000718496
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2007-07-18
Date Posted
2007-10-02
Date Terminated
2008-04-02
Product Code
NKB
Event Number
38449
Product Quantity
11 units
Product Description PathFinder Bone Drill-Awl-Tap, a part of the PathFinder spinal stablization system, Part Number 1156-50.

Reason for Recall Tip of PathFinder surgical instrument broke during procedure.

Action Details Firm notified sales representatives with an approved phone script on 7/18/2007.

Distribution Pattern Nationwide.

Code Information / Serial Numbers Part Numbers 1156-50, lot number 44QR.

Related Establishments / Registrations

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This page represents an index of public-record FDA device recalls. It does not imply current safety or compliance status of the product. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Refer to official government sources for primary safety alerts.

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