PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: March 23, 2016 Initiated: December 23, 2015 #Z-1094-2016

Product Description

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

Reason for Recall

The sterile battery may contain particulates within the sterile package.

Details

Recalling Firm
Pro-Dex Inc
Units Affected
1995 total
Distribution
Distributed in FL.
Location
Irvine, CA

Frequently Asked Questions

What product was recalled?
Battery Pack KLS-SD-1000 Case (40 ct) Models: KLS-BP-040 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).. Recalled by Pro-Dex Inc. Units affected: 1995 total.
Why was this product recalled?
The sterile battery may contain particulates within the sterile package.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 23, 2016. Severity: Moderate. Recall number: Z-1094-2016.