---
title: "KLS Martin Battery Pack, REF: KLS BP2 001, and KLS BP2 040 (bulk case of 40),... — FDA record Z-0280-2025 | Is It on Recall"
description: "The packaging of a sterile battery, intended to power a surgical screwdriver, may contain Tyvek shavings inside the sterile package."
url: https://isitonrecall.com/recall/fda-device-z-0280-2025-kls-martin-battery-pack-ref-kls-bp2-001-and-kls-bp2-040-bulk-case-of-40-used-in-conjunction-with-the/
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 BP2 001, and KLS BP2 040 (bulk case of 40), used in conjunction with the KLS Martin... — FDA record Z-0280-2025

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 Sep 23, 2024. 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 BP2 001, and KLS BP2 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver 2.0 surgical driver, REF: KLS-SD-2000
- **Reason**: The packaging of a sterile battery, intended to power a surgical screwdriver, may contain Tyvek shavings inside the sterile package.
- **Classification**: Class II
- **Recalling firm**: Pro-Dex Inc
- **Quantity**: 2000
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0280-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0280-2025%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 | Lot: REF/UDI-DI: K0UB9: KLS-BP2-001/00856482008122, KLS-BP2-040/10856482008129. KLS-SD-2000/00856482008115 |

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

## Distribution

US distribution to FL only.

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**: Nov 6, 2024
- **Recall initiation date**: Sep 23, 2024
- **Center classification date**: Oct 31, 2024

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-0280-2025%22)

## Related records

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