FDA recall Z-1391-2023

Pro-Dex Inc · Class II · device

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.

Reason for recall

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

Distribution

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

Key facts

Status
Ongoing
Initiation date
2023-02-14
Report date
2023-04-26
Voluntary/Mandated
Voluntary: Firm initiated
Location
Irvine, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1391-2023