# FDA recall Z-1321-2024

> **Preat Corp** · Class II · device recall initiated 2024-02-09.

## Product

Preat Nobel Active/Conical-compatible  RP Titanium Blank, REF 9000967

## Reason for recall

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.

## Distribution

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

## Key facts

- **Recall number:** Z-1321-2024
- **Recalling firm:** Preat Corp
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-02-09
- **Report date:** 2024-03-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Santa Maria, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1321-2024

## Citation

> AI Analytics. FDA recall Z-1321-2024. Retrieved 2026-07-28 from https://api.ai-analytics.org/recall/Z-1321-2024. Source: US FDA. Licensed CC0.

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