---
title: "9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be u... — FDA record Z-2318-2024 | Is It on Recall"
description: "Due to incorrect milled titanium abutment being packaged and labeled."
url: https://isitonrecall.com/recall/fda-device-z-2318-2024-9006767-astra-ev-4-8mm-milled-titanium-abutment-milled-abutments-are-too-be-used-in-conjunction-with/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# 9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous de... — FDA record Z-2318-2024

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 Apr 10, 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**: 9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous dental implant fixture to aid in prosthetic rehabilitation.
- **Reason**: Due to incorrect milled titanium abutment being packaged and labeled.
- **Classification**: Class II
- **Recalling firm**: Preat Corp
- **Quantity**: 7 abutmens
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2318-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2318-2024%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 | Model Number: 9006767 UDI-DI code: 00842092159477 Lot Numbers: ED11-20247825, ED11-20248895, ED11-20249165 and 241588 |

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

## Distribution

U.S.: CA, MO, and NV. O.U.S.: 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/)
- [Missouri](https://isitonrecall.com/state/missouri/)
- [Nevada](https://isitonrecall.com/state/nevada/)

## Dates in the source

- **Report date**: Jul 17, 2024
- **Recall initiation date**: Apr 10, 2024
- **Center classification date**: Jul 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-2318-2024%22)

## Related records

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