Drug recall

7 Hole VL Gridlock Fibula Plate, Part # 300-60-001 NON-STERILE SINGLE USE ONLY; 9 Hole VL Gridlock Fibula…

FDA recall event 71967 · Class II · Trilliant Surgical Ltd.

Key facts

Event ID 71967
Recall numbers Z-2490-2015
Recalling firm Trilliant Surgical Ltd.
Product type Devices
Products 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 #…
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
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…
Initiation date Aug 6, 2015
Report date Sep 9, 2015
Termination date Jan 26, 2017
City Houston
State TX
Country United States
FEI number 3007420745

At a glance

  • 1–9 Products in this recall
  • 1–9 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA drug and product recalls

FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.

Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date:

Browse all FDA drug and product recalls