Every recall we track for Trilliant Surgical, LLC — 13 in all — plus the complaints and injury reports the public filed about them.
Trilliant Surgical recalls 8mm HTR Sterile Hammer Toe Reaming Kit (lot TSL007202) due to potential incorrect reamer types. Affected kits may have two of the same reamer instead of one concave and one convex. Contact for remedy.
Trilliant Surgical recalls 70 units of 3.5mm Aresenal Screw Drill Bits with labeling error that may cause misidentification and traceability issues. Affected items have specific lot numbers.
Trilliant Surgical recalls Gridlock Ankle Screw Driver Bit REF 320-35-003 due to potential failure to retain screws during implant procedures. Affected units include specific lot numbers and part numbers.
Trilliant Surgical recalls Gridlock Ankle Plating instructions due to outdated IFU and sterilization protocols. Updated documents may cause surgical errors if not followed correctly.
Trilliant Surgical recalls outdated instructions for use and cleaning protocols for 3S Hemi Toe Implant. Updated documents may affect surgical safety if not followed correctly.
Trilliant Surgical recalls outdated instructions for use and sterilization protocols for Two-Step Hammertoe implants. Updated protocols may affect safe cleaning and sterilization.
Trilliant Surgical recalls Tiger Headless Cannulated Screw System models due to outdated instructions for use and sterilization protocols. Updated documents are required to prevent potential safety issues.
Trilliant Surgical recalls instructions for use and sterilization protocols for Small Joint Reaming System Model 311-00-001 due to updated dry time parameters in 2018. Affected units have older IFUs and cleaning protocols.
Trilliant Surgical recalls outdated instructions for use and sterilization protocols for Tiger Large Cannulated Screw Systems that could lead to infection if improperly cleaned.
Recall of outdated instructions for use and sterilization protocols for Trilliant Surgical Twist Sublatar Implant System Model 112-00-001 due to revised dry time parameters. Affected units sold in 2018.
Recall of outdated instructions for use and sterilization protocols for Trilliant Surgical Disco Subtalar Implant System Model 112-00-001 due to revised dry time parameters.
Trilliant Surgical recalls Gridlock Plating System instructions for use due to outdated dry time parameters in 2018. Affected units have older IFU versions before Document #900-01-006 Rev. N.
Trilliant Surgical recalls Tiger Cannulated Screw Systems with outdated cleaning protocols that could lead to infection if used improperly. Affected models were sold in 2018.
