TriMed Inc.: Medical Device Recall in 2023 - (Recall #: Z-1101-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

RipCord Syndesmosis Button, REF: STA001K

Product Classification:

Class II

Date Initiated: December 22, 2022

Date Posted: February 15, 2023

Recall Number: Z-1101-2023

Event ID: 91478

Reason for Recall:

Overly aggressive tension on the pull suture, while passing the medial button through a bone/soft tissue tunnel across the fibula and tibia, can exceed its strength causing it to break.

Status: Ongoing

Product Quantity: 76

Code Information:

UDI-DI: 00842188123849, Lot: 85305-01

Distribution Pattern:

US Nationwide distribution in the states of IL, PA, TX, GA, TN, AL, MO, FL, AR, LA, HI, OH, TX, KS

Voluntary or Mandated:

Voluntary: Firm initiated