---
title: "microTargeting Insertion Tube Set, P/N 66-IT-05P, Lot 244517. The intended us... — FDA record Z-0312-2025 | Is It on Recall"
description: "A complaint was received (MDR 3002250546-2024-00003) prompting an investigation. The investigation revealed a schematic for a spacer tube which is too long rela"
url: https://isitonrecall.com/recall/fda-device-z-0312-2025-microtargeting-insertion-tube-set-p-n-66-it-05p-lot-244517-the-intended-use-is-to-accurately-guide-a/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# microTargeting Insertion Tube Set, P/N 66-IT-05P, Lot 244517. The intended use is to accurately guide a microelectrod... — FDA record Z-0312-2025

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 4, 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**: microTargeting Insertion Tube Set, P/N 66-IT-05P, Lot 244517. The intended use is to accurately guide a microelectrode or instrument in the brain during stereotactic functional neurosurgical procedures.
- **Reason**: A complaint was received (MDR 3002250546-2024-00003) prompting an investigation. The investigation revealed a schematic for a spacer tube which is too long relative to the size of other components was included in the build order for Lot 244517 of P/N 66-IT-06P. Use of the product with a spacer tube which is too long could result in intercranial hemorrhaging and brain damage.
- **Classification**: Class I
- **Recalling firm**: FHC, Inc.
- **Quantity**: 8 packs of 5ea (40 total)
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0312-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0312-2025%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 | Package DI: 10873263004323; Contains DI Package: 00873263004326 LOT No. 244517 |

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

## Distribution

Domestic distribution only to the following states: AZ, CA, PA, TN, TX, WA.

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

- [Arizona](https://isitonrecall.com/state/arizona/)
- [California](https://isitonrecall.com/state/california/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Washington](https://isitonrecall.com/state/washington/)

## Dates in the source

- **Report date**: Nov 20, 2024
- **Recall initiation date**: Oct 4, 2024
- **Center classification date**: Nov 8, 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-0312-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [FHC, Inc. records](https://isitonrecall.com/brand/fhc-inc/)