FDA Recall Terminated

PathFinder Cannulated T-Handle Bone Awl, Part Number 1155-2; distributed by Abbott Spine, Inc., Austin, TX 78727.

Recall: Z-1784-2008 · Initiated April 17, 2008

Recall

Recall Number
Z-1784-2008
Event Number
47869
Firm
Abbott Spine
FEI Number
3000718496
Product Code
NKB
Status
Terminated
Root Cause
Device Design
Initiated
April 17, 2008
Posted
September 5, 2008
Terminated
December 2, 2009
Address
12708 Riata Vista Cir, # B-100, Austin, TX, 78727-7167

Description

PathFinder Cannulated T-Handle Bone Awl, Part Number 1155-2; distributed by Abbott Spine, Inc., Austin, TX 78727.

Reason

Breakage - Tips on the Pathfinder Bone Awl may bend or break prematurely. The firm has received internal non-conformances and complaints where the tips of the Awl were worn and damaged. Of the tip breaks, six have had material missing. During the same period, there were 15 complaints reported where the tip broke off at the weld after repeated use (1-3 years). The firm found several possible ca

Action

Phone calls and emails were used to disseminate information about this recall. Firm notified consignees via telephone beginning on 04/17/08. Consignees were told that some problems were found through normal wear and tear as well as product mis-use and material weaknesses. The firm explained that they noticed from wear and tear from use as well as damage from use could cause the tip to become dull and flared causing breakage. The firm explained that they redesigned the awl and requested that consignees return outstanding inventory, which will be replaced with a new version of the awl.

Distribution

Class II Recall - Worldwide Distribution --- USA including states of AR, AZ, CA, CT, CO, FL, IL, MD, MI, MO, MT, NC, NJ, NV, NY, NM, OH, OK, PA, SD, TX and WI, and countries of Argentina, Australia, Belgium, Canada, China, Columbia, Cyprus, Germany, Greece, Italy, Japan, Mexico, Thailand, Turkey and UK/Ireland.

Quantity

180 units.