Pro-Dex Inc: Medical Device Recall in 2023 - (Recall #: Z-1391-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: February 14, 2023

Date Posted: April 26, 2023

Recall Number: Z-1391-2023

Event ID: 91850

Reason for Recall:

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

Status: Ongoing

Product Quantity: 199 devices

Code Information:

Reference Number: PDEC-1000-2 Part Number: A9671 Lot Numbers: K0C1B, K0D3P, K0E8T, K0FSD, K0HGV

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated