Exactech, Inc.: Medical Device Recall in 2017 - (Recall #: Z-2704-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Exactech Optetrak Logic CC 15mm Tibial Augment Screws

Product Classification:

Class II

Date Initiated: April 7, 2017

Date Posted: July 19, 2017

Recall Number: Z-2704-2017

Event ID: 77514

Reason for Recall:

Missing Screw in carton. Nine (9) serial numbers were identified as being inadvertently packaged as one per carton when two per carton are required.

Status: Terminated

Product Quantity: 9 devices

Code Information:

Catalog No. 02-012-50-9015; Serial #'s 4739530, 4739531, 4739532, 4739533, 4739534, 4739535, 4739536, 4739537, and 4739538.

Distribution Pattern:

CA and NY.

Voluntary or Mandated:

Voluntary: Firm initiated