FDA Recall Terminated

7 Hole VL Gridlock Fibula Plate, Part # 300-60-001 NON-STERILE SINGLE USE ONLY; 9 Hole VL Gridlock Fibula Plate, Part # 300-60-002 NON-STERILE SINGLE USE ONLY; 11 Hole VL Gridlock Fibula Plate, Part # 300-60-003 NON-STERILE SINGLE USE ONLY. For use in trauma and reconstructive procedures in small bones.

Recall: Z-2490-2015 · Initiated August 6, 2015

Recall

Recall Number
Z-2490-2015
Event Number
71967
Firm
Trilliant Surgical Ltd.
FEI Number
3007420745
Product Code
HRS
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
August 6, 2015
Posted
August 31, 2015
Terminated
January 26, 2017
Address
6721 Portwest Dr, Ste 160, Houston, TX, 77024-8019

Description

7 Hole VL Gridlock Fibula Plate, Part # 300-60-001 NON-STERILE SINGLE USE ONLY; 9 Hole VL Gridlock Fibula Plate, Part # 300-60-002 NON-STERILE SINGLE USE ONLY; 11 Hole VL Gridlock Fibula Plate, Part # 300-60-003 NON-STERILE SINGLE USE ONLY. For use in trauma and reconstructive procedures in small bones.

Reason

The affected parts subject to the recall are out of specification, resulting in in the loss of the optimal locking screw functionality of the plates. The thread depth of the screw holes is insufficient, potentially limiting the ability to engage and lock with associated mating locking screws.

Action

Trilliant Surgical sent an Urgent Medical Device Recall letter dated August 13, 2015, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. The letter instructed and confirmed consignees to discontinue use of the affected lots, quarantine, and return product (if not yet done so) in accordance with an included acknowledgement sheet. For further questions, please call 1(800) 495-2919 , 8:00am - 5:00pm CST

Distribution

US Distribution to the states of : FL, OH, NJ, MN, WI, NM and CA.

Quantity

28 units