Trilliant Surgical Ltd.

Complete recall history across all FDA and CPSC categories — 10 total recalls

Trilliant Surgical Ltd. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (10)

FDA medical device enforcement actions by Trilliant Surgical Ltd.

Date Product Reason Class
Mar 27, 2018 Cannulated Driver Handle, Catalog #: 210-00-003, Rx Only, Non Sterile Firm is voluntarily recalling cannulated driver handles (210-00-003 and 210-0... Class II
Mar 27, 2018 Ratcheting Cannulated Driver Handle, Catalog #: 210-00-004, Rx Only, Non Sterile Firm is voluntarily recalling cannulated driver handles (210-00-003 and 210-0... Class II
Dec 8, 2016 Tiger Screw Sterilization Tray Base Assembly Model 210-00-001 Revision N, O ... Four lots of Tiger Screw Sterilization Tray Base Assemblies were released to ... Class II
Sep 2, 2016 Model 208-70-110, Long Thread Tiger Large Cannulated Headless Screw, 7 x 110 ... Screws were identified as having the incorrect part number and lot number mar... Class II
Aug 6, 2015 7 Hole VL Gridlock Fibula Plate, Part # 300-60-001 NON-STERILE SINGLE USE ONL... The affected parts subject to the recall are out of specification, resulting ... Class II
Jul 31, 2015 2.4, 3.0, and 4.0 mm Gridlock Screw Driver Bit, Model Number 310-30-003, Lot ... Gridlock screw driver bits for the Gridlock Plating System were identified to... Class II
Jul 20, 2015 3.0/4.0 Cannulated Drill Bit; a component of the Tiger Cannulated Screw Syste... The cannulation of the 3.0/4.0 Cannulated Drill Bit inner diamter is too smal... Class II
Jul 20, 2015 2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and 3.0/4.... The cutting efficiency of the Countersinks was out of specification. Class II
Jul 20, 2015 Tiger Cannulated Tray Lid Part # 210-00-001-1 NON-STERILE; Combined Tiger/Hea... Sterilization tray lids for the Tiger and Tiger Headless Cannulated Screw Sys... Class II
Jul 20, 2015 Concave Reamer Head, 16 mm; Concave Reamer Head, 18 mm; Concave Reamer Head, ... The cannulation of the Concave and Convex Reamer Heads may be too small to al... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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