---
title: "NaviNetics Skull Anchor Key and Drill Kit, REF NN1215 — FDA record Z-1478-2024 | Is It on Recall"
description: "Defective Skull Anchor Key. After attachment of the single use Skull Anchor Key to the patient, the user was unable to attach the CT Localizer to perform stereo"
url: https://isitonrecall.com/recall/fda-device-z-1478-2024-navinetics-skull-anchor-key-and-drill-kit-ref-nn1215/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# NaviNetics Skull Anchor Key and Drill Kit, REF NN1215 — FDA record Z-1478-2024

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 26, 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**: NaviNetics Skull Anchor Key and Drill Kit, REF NN1215
- **Reason**: Defective Skull Anchor Key. After attachment of the single use Skull Anchor Key to the patient, the user was unable to attach the CT Localizer to perform stereotactic Imaging. Attachment of the localizer is typically accomplished by fully screwing in the four thumbscrews of the localizer into the threaded holes found on the top surface of the Skull Anchor Key.
- **Classification**: Class II
- **Recalling firm**: Navinetics Inc
- **Quantity**: 20 kits
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1478-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1478-2024%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 | UDI/DI 10850023620276, Lot Number 331401724 |

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

## Distribution

US Nationwide distribution in the states of FL, MN, CO.

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

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## Dates in the source

- **Report date**: Apr 10, 2024
- **Recall initiation date**: Feb 26, 2024
- **Center classification date**: Apr 4, 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-1478-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Navinetics Inc records](https://isitonrecall.com/brand/navinetics-inc/)