Trilliant Surgical Ltd.: Medical Device Recall in 2018 - (Recall #: Z-2338-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Cannulated Driver Handle, Catalog #: 210-00-003, Rx Only, Non Sterile

Product Classification:

Class II

Date Initiated: March 27, 2018

Date Posted: July 11, 2018

Recall Number: Z-2338-2018

Event ID: 80195

Reason for Recall:

Firm is voluntarily recalling cannulated driver handles (210-00-003 and 210-00-004) that may demonstrate a degradation of function with the adapter collar sticking, and/or not retaining the mating adapter male shaft.

Status: Terminated

Product Quantity: 94

Code Information:

Lot: 603599

Distribution Pattern:

U.S. States: NE, MA, GA, TX, OR, AZ, FL, OH, WA, NJ, UT, VA, CA, MN, PA, DE, OK, KS, WI, MT, IA, MO

Voluntary or Mandated:

Voluntary: Firm initiated