---
title: "Preat REF 9007123, Neodent GM x 4mm Healing Abutment, Rx Only, Non-Sterile, S... — FDA record Z-0153-2024 | Is It on Recall"
description: "The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage"
url: https://isitonrecall.com/recall/fda-device-z-0153-2024-preat-ref-9007123-neodent-gm-x-4mm-healing-abutment-rx-only-non-sterile-single-use-only-dental/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Preat REF 9007123, Neodent GM x 4mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental — FDA record Z-0153-2024

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 Jul 18, 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**: Preat REF 9007123, Neodent GM x 4mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental
- **Reason**: The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage
- **Classification**: Class II
- **Recalling firm**: Preat Corp
- **Quantity**: 23 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0153-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0153-2024%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: 00842092161388/Lot #OF018357 |

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

## Distribution

US: FL, CA, OR, TX, OH, CA, SC, OR, NJ, SC, OUS: None

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

- [California](https://isitonrecall.com/state/california/)
- [Florida](https://isitonrecall.com/state/florida/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Oregon](https://isitonrecall.com/state/oregon/)
- [South Carolina](https://isitonrecall.com/state/south-carolina/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Nov 1, 2023
- **Recall initiation date**: Jul 18, 2023
- **Center classification date**: Oct 23, 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-0153-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Preat Corp records](https://isitonrecall.com/brand/preat-corp/)