Exactech, Inc.: Medical Device Recall in 2013 - (Recall #: Z-1832-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Exactech Articulated Driver A nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery.

Product Classification:

Class II

Date Initiated: May 30, 2013

Date Posted: August 7, 2013

Recall Number: Z-1832-2013

Event ID: 65568

Reason for Recall:

When torque is applied to the Articulated Driver at the maximum angle, the cross pin may shift out of position, potentially leading to disassembly of the instrument.

Status: Terminated

Product Quantity: 57

Code Information:

Lot #: 52667001 Catalog #: 181-00-04

Distribution Pattern:

US Distribution including the states of AR, CA, FL, NJ, NY, OK, and TX

Voluntary or Mandated:

Voluntary: Firm initiated