Pro-Dex Inc recalls KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly used to connect the KLS driver (e

Recalled April 26, 2023 · FDA recall Z-1391-2023 · Pro-Dex

Hazard

Incorrect Unique Device Identifier/GTIN code was used on product. · FDA Class II

Units

199 devices

Sold at

U.S. Nationwide distribution in the state of FL.

Description

Incorrect Unique Device Identifier/GTIN code was used on product.

Product

KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly used to connect the KLS driver (e.g. drill) to a driver bit that fits into the adapter.

Manufacturer(s)

Pro-Dex Inc

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