Pro-Dex Inc recalls Battery Pack KLS-SD-1000 Case (40 ct) Models: KLS-BP-040 Used to power the KLS Martin Max Driver (battery powdered

Recalled March 23, 2016 · FDA recall Z-1094-2016 · Pro-Dex

Hazard

The sterile battery may contain particulates within the sterile package. · FDA Class II

Units

1995 total

Sold at

Distributed in FL.

Description

The sterile battery may contain particulates within the sterile package.

Product

Battery Pack KLS-SD-1000 Case (40 ct) Models: KLS-BP-040 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).

Manufacturer(s)

Pro-Dex Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →