---
title: "KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), u... — FDA record Z-2098-2023 | Is It on Recall"
description: "Battery packs used in surgical procedures where a surgeon uses a powered screwdriver and a right-angle attachment have switched manufacturing and expiration dat"
url: https://isitonrecall.com/recall/fda-device-z-2098-2023-kls-martin-battery-pack-ref-kls-bp-001-and-kls-bp-040-bulk-case-of-40-used-in-conjunction-with-the-k/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction with the KLS Martin M... — FDA record Z-2098-2023

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Feb 15, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver
- **Reason**: Battery packs used in surgical procedures where a surgeon uses a powered screwdriver and a right-angle attachment have switched manufacturing and expiration dates on sterile pouch labels, so batteries will appear to be prematurely expired.
- **Classification**: Class II
- **Recalling firm**: Pro-Dex Inc
- **Quantity**: 2000
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2098-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2098-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | REF: KLS-BP-001/KLS-BP-040, UDI-DI: 00862377000140, Lot: K0M6U, Expiration: 8/31/2024 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US: FL

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Florida](https://isitonrecall.com/state/florida/)

## Dates in the source

- **Report date**: Jul 12, 2023
- **Recall initiation date**: Feb 15, 2023
- **Center classification date**: Jul 5, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2098-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Pro-Dex Inc records](https://isitonrecall.com/brand/pro-dex-inc/)