Trilliant Surgical Ltd.: Medical Device Recall in 2015 - (Recall #: Z-2490-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product 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.

Product Classification:

Class II

Date Initiated: August 6, 2015

Date Posted: September 9, 2015

Recall Number: Z-2490-2015

Event ID: 71967

Reason for Recall:

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.

Status: Terminated

Product Quantity: 28 units

Code Information:

Lots: TSL002595, TSL002596, TSL002597

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated