---
title: "Small DKS Disposable Kerrison System, Catalog Number DKS-63030, instrument se... — FDA record Z-0651-2025 | Is It on Recall"
description: "Units were not intended for commercial distribution and inadvertently distributed."
url: https://isitonrecall.com/recall/fda-device-z-0651-2025-small-dks-disposable-kerrison-system-catalog-number-dks-63030-instrument-sets-that-come-in-two-sizes/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Small DKS Disposable Kerrison System, Catalog Number DKS-63030, instrument sets that come in two sizes (3.75mm and 6.... — FDA record Z-0651-2025

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 Oct 30, 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**: Small DKS Disposable Kerrison System, Catalog Number DKS-63030, instrument sets that come in two sizes (3.75mm and 6.35mm) containing: 1. DKS Small Obturator Trocar (Model Number 330.013) 2. DKs Small Lighted Cannula (Model Number 330.014) 3. DKS Small Kerrison (330.016)
- **Reason**: Units were not intended for commercial distribution and inadvertently distributed.
- **Classification**: Class II
- **Recalling firm**: Folsom Metal Products, Inc.
- **Quantity**: 6 sets
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0651-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0651-2025%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 | Catalog Number DKS-63030, Lot Number: 1578. |

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

## Distribution

US distribution to KS, LA, MI, NY, TX.

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

- [Kansas](https://isitonrecall.com/state/kansas/)
- [Louisiana](https://isitonrecall.com/state/louisiana/)
- [Michigan](https://isitonrecall.com/state/michigan/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Dec 18, 2024
- **Recall initiation date**: Oct 30, 2023
- **Center classification date**: Dec 6, 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-0651-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Folsom Metal Products, Inc. records](https://isitonrecall.com/brand/folsom-metal-products-inc/)