FDA Recall Terminated

2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and 3.0/4.0 Cannulated Screw Countersink Part # 210-40-002 NON-STERILE Product Usage: 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.

Recall: Z-2421-2015 · Initiated July 20, 2015

Recall

Recall Number
Z-2421-2015
Event Number
71783
Firm
Trilliant Surgical Ltd.
FEI Number
3007420745
Product Code
HWC
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
July 20, 2015
Posted
August 19, 2015
Terminated
January 26, 2017
Address
6721 Portwest Dr, Ste 160, Houston, TX, 77024-8019

Description

2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and 3.0/4.0 Cannulated Screw Countersink Part # 210-40-002 NON-STERILE Product Usage: 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.

Reason

The cutting efficiency of the Countersinks was out of specification.

Action

Trilliant sent an Important Medical Device Advisory Notice letter dated February 15, 2013 to affected customers. The letter identified the affected product, problem and actions to be taken. The letter informed customers of the option to exchange affected instruments at no charge. To initiate the exchange customers were instructed to contact your local Trilliant Surgical Sales Representative, contact the Customer Service Department directly at 1-800-495-2919, or via email at [email protected].

Distribution

US Nationwide Distribution in the states of: NY, CT, TN, TX, OH, IN, LA, NC, MO, MN, GA, FL, SC, WA, WI, IA, PA, CA, ND, OK, NJ, MI and MD.

Quantity

102 units