The Recall Desk

Manufacturer

Trilliant Surgical, LLC

13 recalls in our database name Trilliant Surgical, LLC as the manufacturing or recalling firm.

What the numbers show

Total
13
Critical
0
Severe
1
Most recent
2020-05-13

Of the 13 recalls from Trilliant Surgical, LLC we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (8%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–13 of 13

  • ModerateFDA (Devices)·Z-1892-2020·2020-05-13

    Trilliant Surgical Recalls 3.5mm Aresenal Screw Drill Bits Due to Labeling Error

    Trilliant Surgical, LLC is recalling 3.5mm Aresenal Screw Drill Bits due to a labeling error where the lot number is incorrectly marked, potentially impacting device traceability.

    Product
    3.5mm Aresenal Screw Drill Bit , Ref: 330-35-001, Qty. 70, Rx Only, Non-Sterile, UDI: (01)00812926029696 - Product Usage: A drill bit facilitates implant insertion
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1614-2020·2020-04-08

    Trilliant Surgical Small Joint Reaming System Instructions for Use Recall

    Trilliant Surgical LLC is recalling Instructions for Use and Cleaning Protocols for the Small Joint Reaming System to update dry time parameters.

    Product
    Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd Small Joint Reaming System, Model 311-00-001. The firm name on the label is Trilliant Surgical Ltd, Houston, TX.
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-1635-2020·2020-04-08

    Trilliant Surgical Recalls 8mm Hammer Toe Reaming Kits Due to Incorrect Contents

    Trilliant Surgical is recalling 117 units of 8mm HTR Sterile Hammer Toe Reaming Kits because they may contain two identical reamers instead of one concave and one convex reamer.

    Product
    8mm HTR Sterile Hammer Toe Reaming Kit, Material: Stainless Steel, Sterile: R, PX only, UDI: (01)00812926022345(17)231225 (10)TSL007202
    Category
    Medical Device
    Distribution
    21 states
  • ModerateFDA (Devices)·Z-1612-2020·2020-04-08

    Trilliant Surgical Recalls Instructions for Use for Cannulated Screw Systems

    Trilliant Surgical, LLC is recalling Instructions for Use and Surgical Cleaning and Sterilization Protocols for two cannulated screw systems to update dry time parameters.

    Product
    Instructions for Use and Surgical Cleaning and Sterilization Protocol for: (1) Trilliant Surgical Ltd Tiger Large Cannulated Screw System, Model 215-00-001; and (2) Trilliant Surgical Ltd Large Cannulated Headless Screw System, Model 215-00-001. The firm name on the labe
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-1605-2020·2020-04-08

    Trilliant Surgical Recalls Instructions for Use for Tiger Screw Systems

    Trilliant Surgical is recalling Instructions for Use and Cleaning Protocols for Tiger Cannulated Screw Systems to update dry time parameters.

    Product
    Instructions for Use and Surgical Cleaning and Sterilization Protocol for: (1) Trilliant Surgical Tiger Cannulated Screw System, Model 210-00-001; and (2) Combination Tiger/Tiger Headless Cannulated Screw System, Model 210-00-101. The firm name on the label is Trilliant S
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-1609-2020·2020-04-08

    Trilliant Surgical Gridlock Plating System Instructions for Use Recall

    Trilliant Surgical is recalling Instructions for Use and Cleaning Protocols for the Gridlock Plating System to update dry time parameters.

    Product
    Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd Gridlock Plating System, Model 310-01-100. The firm name on the label is Trilliant Surgical Ltd, Houston, TX.
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-1610-2020·2020-04-08

    Trilliant Surgical Recalls Hammertoe Implant Instructions for Use

    Trilliant Surgical is recalling Instructions for Use and Cleaning Protocols for its Two-Step Hammertoe Implant System to update dry time parameters.

    Product
    Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd Two-Step Hammertoe Implant System, Model 214-00-001. The firm name on the label is Trilliant Surgical Ltd, Houston, TX.
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-1608-2020·2020-04-08

    Trilliant Surgical Disco Subtalar Implant Instructions for Use Recall

    Trilliant Surgical, LLC is recalling Instructions for Use and Surgical Cleaning and Sterilization Protocols for the Disco Subtalar Implant System to update dry time parameters.

    Product
    Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd Disco Subtalar Implant System, Model 112-00-001. The firm name on the label is Trilliant Surgical, Ltd, Houston, TX.
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-1607-2020·2020-04-08

    Trilliant Surgical Twist Sublatar Implant System Instructions for Use Recall

    Trilliant Surgical, LLC is recalling Instructions for Use and Surgical Cleaning and Sterilization Protocols for the Twist Sublatar Implant System to update dry time parameters.

    Product
    Instructions for Use and Surgical Cleaning Sterilization Protocol for Trilliant Surgical Ltd Twist Sublatar Implant System, Model 112-00-001. The firm name on the label is Trilliant Surgical, Ltd, Houston, TX.
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-1611-2020·2020-04-08

    Trilliant Surgical 3S Hemi Toe Implant Instructions for Use Recall

    Trilliant Surgical is recalling Instructions for Use and Cleaning Protocols for the 3S Hemi Toe Implant System to update dry time parameters.

    Product
    Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd 3S Hemi Toe Implant System, Model 111-00-001. The firm name on the label is Trilliant Surgical Ltd, Houston, TX.
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-1606-2020·2020-04-08

    Trilliant Surgical Recalls Instructions for Use for Tiger Screw Systems

    Trilliant Surgical is recalling Instructions for Use and Cleaning Protocols for Tiger Screw Systems to update dry time parameters.

    Product
    Instructions for Use and Surgical Cleaning and Sterilization Protocol for: (1) Trilliant Surgical Ltd Tiger Headless Cannulated Screw System, Model 212-00-001; and (2) Combination Tiger Cannulated/Tiger Headless Cannulated Screw System, Model 210-00-101. The firm name on
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-1613-2020·2020-04-08

    Trilliant Surgical Gridlock Ankle Plating System Instructions for Use Recalled

    Trilliant Surgical LLC is recalling Instructions for Use and Surgical Cleaning and Sterilization Protocols for the Gridlock Ankle Plating System to update dry time parameters.

    Product
    Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd Gridlock Ankle Plating System, Model 320-01-100. The firm name on the label is Trilliant Surgical Ltd, Houston, TX.
    Category
    Medical Device
    Distribution
    29 states
  • SevereFDA (Devices)·Z-0799-2020·2020-01-22

    Trilliant Gridlock Ankle Screw Driver Bit Recalled for Specification Defect

    Trilliant Surgical is recalling 20 Gridlock Ankle Screw Driver Bits because they are out of specification and may fail to retain screws during implant procedures.

    Product
    Gridlock Ankle Screw Driver Bit REF 320-35-003 - Product Usage: A screwdriver facilitates implant insertion and removal.
    Category
    Medical Device
    Distribution
    Distributed nationwide