Trilliant Surgical Ltd.: Medical Device Recall in 2015 - (Recall #: Z-2452-2015)

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:

3.0/4.0 Cannulated Drill Bit; a component of the Tiger Cannulated Screw System The Tiger Cannulated Screw Fixation System implants are intended for fixation of fractures, non-unions, arthrodesis and osteotomies of the small bones in the hand and foot. The implants and guide wires are intended for single use only.

Product Classification:

Class II

Date Initiated: July 20, 2015

Date Posted: September 2, 2015

Recall Number: Z-2452-2015

Event ID: 71812

Reason for Recall:

The cannulation of the 3.0/4.0 Cannulated Drill Bit inner diamter is too small to allow for the guide wire to pass completely through.

Status: Terminated

Product Quantity: 121 units

Code Information:

Lot 1363-01

Distribution Pattern:

Nationwide Distribution including NY, TX, OH, IN, FL, NH, MN, SC, OK, NJ, CA, NC, MO, GA, WI, IA, TN, WA, and Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated