# FDA recall Z-1391-2023

> **Pro-Dex Inc** · Class II · device recall initiated 2023-02-14.

## 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

- **Recall number:** Z-1391-2023
- **Recalling firm:** Pro-Dex Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-02-14
- **Report date:** 2023-04-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Irvine, CA, United States

## Primary source

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

## Citation

> AI Analytics. FDA recall Z-1391-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1391-2023. Source: US FDA. Licensed CC0.

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