FDA Recall Terminated

Stryker Xia 3 Anti-Torque Key Manual Surgical Instrument; Catalog Number 48237026. Product Usage: : Reusable instrument used to aid in the final tightening of the spinal construct. Intended Use: The Anti-Torque Key allows the Torque Wrench to align with the tightening axis and maximizing the torque needed to lock the implant assembly during final tightening of the spinal construct.

Recall: Z-1706-2012 · Initiated January 12, 2012

Recall

Recall Number
Z-1706-2012
Event Number
61766
Firm
Stryker Spine
FEI Number
3004024955
Product Code
NKB
Status
Terminated
Root Cause
Mixed-up of materials/components
Initiated
January 12, 2012
Posted
June 5, 2012
Terminated
March 21, 2013
Address
2 Pearl Ct, Allendale, NJ, 07401-1611

Description

Stryker Xia 3 Anti-Torque Key Manual Surgical Instrument; Catalog Number 48237026. Product Usage: : Reusable instrument used to aid in the final tightening of the spinal construct. Intended Use: The Anti-Torque Key allows the Torque Wrench to align with the tightening axis and maximizing the torque needed to lock the implant assembly during final tightening of the spinal construct.

Reason

Stryker received four reports regarding a handle which separates at the point where it is welded to the shaft on the Xia 3 Anti-Torque Key during surgery.

Action

Stryker Spine sent an Urgent Product Recall letter dated January 12, 2012 with an attached Customer Response forms via FEDEX to affected customers. The letter identified the affected product, problem and actions to be taken. Customers were instructed to examine their inventory to identify the affected product and return using the prepaid mailing label provided. The letter asked customers to complete the Customer Response Form and fax to 201.760.8370. For questions call 201.760.8298.

Distribution

US Nationwide Distribution

Quantity

95 units