TriMed Inc.: Medical Device Recall in 2018 - (Recall #: Z-1373-2018)

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:

Hex Driver Part Number HXDRIVER-2.0 AO; Hex Driver Part Number HXDRIVR-2.5 AO; Hex Driver Part Number HXDRIVR-2.5CL AO; Hex Driver Part Number DVHX-2.5/130C AO; Hex Driver Part Number HXDRIVR-3.0 AO; Hex Driver Part Number HXDRIVER-3.5AO

Product Classification:

Class II

Date Initiated: January 11, 2018

Date Posted: April 18, 2018

Recall Number: Z-1373-2018

Event ID: 79224

Reason for Recall:

Following the completion of sterilization cycle(s) of the impacted Hex Driver, the epoxy color band on the impacted Hex Driver can migrate down the shaft and/or potentially onto the sterilization tray or caddy.

Status: Terminated

Product Quantity: 1525 devices

Code Information:

Affected lot numbers: 922361, 922362, 91956, 91957, 92237, 92238, 91858, 92235, 92656, 91856, 91857

Distribution Pattern:

US, China, Latin America

Voluntary or Mandated:

Voluntary: Firm initiated