FDA Recall Terminated

JTS External Drive Unit JTS Distal Femoral Extendible Implant Femur is intended for the replacement of diseased or deficient bone in the distal femur.

Recall: Z-3104-2017 · Initiated July 4, 2017

Recall

Recall Number
Z-3104-2017
Event Number
77753
Firm
Stanmore Implants Worldwide Ltd. Centennial Park
FEI Number
3004105610
Product Code
KRO
Status
Terminated
Root Cause
Labeling design
Initiated
July 4, 2017
Terminated
February 16, 2021
Address
210 Centennial Avenue, CENTENNIAL PARK Borehamwood United Kingdom

Description

JTS External Drive Unit JTS Distal Femoral Extendible Implant Femur is intended for the replacement of diseased or deficient bone in the distal femur.

Reason

Three (3) complaints were identified in which the potential for utilization of the JTS Grower Drive in the incorrect orientation in relation to the limb entry point of the device, together with the potential to select incorrect settings for the extension procedure. As a result, the prostheses in such cases failed to extend as intended.

Action

Stanmore Implants sent an Urgent Field Safety Notice dated July 4, 2017, notifying customers of the recall. Additionally, the recalling firm requests that consignees immediately check their inventory for recalled product, quarantine any product on hand, inform SIW of any product on hand, complete the attached response form, and return the response for and affected product to the firm. It is requested that consignees distribute the notice internally to all affected parties and that they contact their local Stanmore representative to request training. If any adverse events are associated with this device, the firm asks that it be reported to them. For further questions, please call (972) 501-1402.

Distribution

US Distribution to the states of : CA, FL, GA, KS, MI, NJ, OH, PA, SC, and TX.

Quantity

15 units