FDA Recall Terminated

Firebird Spinal Fixation System Torque Limiting Handle (PN 52-1512) Intended for posterior, non-cervical pedicle, and non-pedicle fixation (T1-S2/llium).

Recall: Z-0797-2016 · Initiated January 8, 2016

Recall

Recall Number
Z-0797-2016
Event Number
73069
Firm
Orthofix, Inc
FEI Number
2183449
Product Code
HXC
Status
Terminated
Root Cause
Component design/selection
Initiated
January 8, 2016
Posted
February 11, 2016
Terminated
November 16, 2016
Address
3451 Plano Pkwy, Lewisville, TX, 75056-9453

Description

Firebird Spinal Fixation System Torque Limiting Handle (PN 52-1512) Intended for posterior, non-cervical pedicle, and non-pedicle fixation (T1-S2/llium).

Reason

There is a possibility that the device may deliver a torque value less than the required setting after initial sterilization. In worst case, the unexpected drop in torque value may lead to the spinal construct loosening and requiring corrective surgical intervention.

Action

Affected consignees were notified via an Urgent Medical Device Recall Notification letter, dated 1/8/16. The letter identified the affected device and stated the reason for the recall. The recalling firm requests customers to remove the affected devices from their inventory and cease further distribution or use. Customers whom the devices were further distributed to should be notified that the affected devices cannot be used and must be returned to Orthofix per the instructions provided. The attached Acknowledgement Form should be completed and returned. Customers can contact their local Orthofix representative or customer service for further information, replacements, or disposal instructions.

Distribution

Worldwide Distribution -- US, Spain, Italy, and Australia.

Quantity

36 units