FDA Recall Terminated

Firebird NXG Spinal Fixation System Decorticating Planer, Catalog #36-1334, non-sterile, Rx. .A Decorticating Planer is used to decorticate bone surrounding the spherical head of an implanted bone screw in order to provide clearance to allow for proper seating of the modular body, as well as to provide full range of modular body angulation. It is placed axially over the spherical head of the bone screw and rotated clockwise and counterclockwise to achieve the needed decortication

Recall: Z-3127-2017 · Initiated August 2, 2017

Recall

Recall Number
Z-3127-2017
Event Number
77882
Firm
Orthofix, Inc
FEI Number
2183449
Product Code
NKB
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
August 2, 2017
Posted
August 18, 2017
Terminated
May 4, 2018
Address
3451 Plano Pkwy, Lewisville, TX, 75056-9453

Description

Firebird NXG Spinal Fixation System Decorticating Planer, Catalog #36-1334, non-sterile, Rx. .A Decorticating Planer is used to decorticate bone surrounding the spherical head of an implanted bone screw in order to provide clearance to allow for proper seating of the modular body, as well as to provide full range of modular body angulation. It is placed axially over the spherical head of the bone screw and rotated clockwise and counterclockwise to achieve the needed decortication

Reason

The plastic core of the Decorticating Planer was found to be missing, which could result in scoring of the bone screw neck if used at or beyond a 23 degree angle.

Action

Orthofix sent an Urgent Medical Device Product Recall letter dated August 2, 2017, to all affected customers. The letter explained the issue and requested return of product in their possession. Customers with questions were instructed to contact their local Orthofix representative. For questions regarding this recall call 214-937-2100.

Distribution

Distribution was made to distributors located in CA, FL, and RI. There was no foreign/military/government distribution.

Quantity

6 planers