Pro-Dex Inc recalls KLS Martin Battery Pack, REF: KLS BP2 001, and KLS BP2 040 (bulk case of 40), used in conjunction with the KLS Martin Ma

Recalled November 6, 2024 · FDA recall Z-0280-2025 · Pro-Dex

Hazard

The packaging of a sterile battery, intended to power a surgical screwdriver, may contain Tyvek shavings inside the sterile package. · FDA Class II

Units

2000

Sold at

US distribution to FL only.

Description

The packaging of a sterile battery, intended to power a surgical screwdriver, may contain Tyvek shavings inside the sterile package.

Product

KLS Martin Battery Pack, REF: KLS BP2 001, and KLS BP2 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver 2.0 surgical driver, REF: KLS-SD-2000

Manufacturer(s)

Pro-Dex Inc

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