---
title: "Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967 — FDA record Z-1321-2024 | Is It on Recall"
description: "Due to a manufacturing issue, the screw seat location on the abutment product may be too high, causing mating screw to have a shorter engagement length into the"
url: https://isitonrecall.com/recall/fda-device-z-1321-2024-preat-nobel-active-conical-compatible-rp-titanium-blank-ref-9000967/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967 — FDA record Z-1321-2024

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 9, 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**: Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
- **Reason**: Due to a manufacturing issue, the screw seat location on the abutment product may be too high, causing mating screw to have a shorter engagement length into the associated implant.
- **Classification**: Class II
- **Recalling firm**: Preat Corp
- **Quantity**: 561 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1321-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1321-2024%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: 9000967 UDI-DI code: 00842092165867 Lot Numbers: 235650, 234294, 233667, 233885, 233439, and 231489 |

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

## Distribution

U.S. Nationwide distribution in the states of AZ, OH and PA.

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

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- [Oregon](https://isitonrecall.com/state/oregon/)
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- [Rhode Island](https://isitonrecall.com/state/rhode-island/)
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- [South Dakota](https://isitonrecall.com/state/south-dakota/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Mar 27, 2024
- **Recall initiation date**: Feb 9, 2024
- **Center classification date**: Mar 20, 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-1321-2024%22)

## Related records

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