Pro-Dex Inc: Medical Device Recall in 2016 - (Recall #: Z-1095-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Battery Pack KLS-SD-1000 Single Models: KLS-BP-001 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).

Product Classification:

Class II

Date Initiated: December 23, 2015

Date Posted: March 23, 2016

Recall Number: Z-1095-2016

Event ID: 73034

Reason for Recall:

The sterile battery may contain particulates within the sterile package.

Status: Terminated

Product Quantity: 1995 total

Code Information:

Lots 509567, K055R

Distribution Pattern:

Distributed in FL.

Voluntary or Mandated:

Voluntary: Firm initiated