# FDA recall Z-2687-2024

> **Preat Corp** · Class II · device recall initiated 2024-06-25.

## Product

Multiple Digital Analog Products labeled as:  NobelBiocare Tri-Lobe-compatible 6.0mm Digital Analog, REF 9000703  Straumann Tissue-Level-compatible WN Digital Analog, REF 9001303  3i Certain-compatible 5.0mm Digital Analog, REF 9001903  3i Certain-compatible 6.0mm Digital Analog, REF 9002003  Astra-compatible 3.0mm Digital Analog, REF 9002103  Astra-compatible Aqua 3.5/4.0mm Digital Analog, REF 9002203  Astra-compatible Lilac 4.5/5.0mm Digital Analog, REF 9002203  BioHorizons¿-compatible 3.0mm Digital Analog, REF 9005203  Legacy-compatible 3.0mm Digital Analog, REF 9005303  Digital Analog - BioHorizons - 3.5mm, Digital Analog - BioHorizons¿ - 4.5mnm, REF 9005403  Legacy-compatible 3.5mm Digital Analog, REF 9005503  Legacy-compatible 5.7mm Digital Analog, REF 9008503  Astra EV 4.8mm Milled Titanium Abutment REF 9006767    Digital analogs are used for visual inspection of abutments and restoration in the dental laboratory.

## Reason for recall

Due to a manufacturing issue, the product has a out of specification rotation of the digital analog used to visually inspect dental abutments and restorations.

## Distribution

U.S. Nationwide distribution in the states of  AK, AZ, FL, GA, IL, LA, MD, MI, MN, NY, OH, OK, OR, PA, RI, TX, UT, and WA

## Key facts

- **Recall number:** Z-2687-2024
- **Recalling firm:** Preat Corp
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-25
- **Report date:** 2024-08-28

- **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-2687-2024

## Citation

> AI Analytics. FDA recall Z-2687-2024. Retrieved 2026-07-13 from https://api.ai-analytics.org/recall/Z-2687-2024. Source: US FDA. Licensed CC0.

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