# FDA recall Z-2951-2020

> **SICAT GMBH & CO. KG** · Class II · device recall initiated 2020-07-15.

## Product

SICAT IMPLANT V2.0

## Reason for recall

A dentist found implant positions are not correctly exported from the implant planning software SICAT IMPLANT V2.0 - for the specific export format CMG.DXD.

## Distribution

Worldwide distribution

## Key facts

- **Recall number:** Z-2951-2020
- **Recalling firm:** SICAT GMBH & CO. KG
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-07-15
- **Report date:** 2020-09-16
- **Termination date:** 2024-01-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bonn, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2951-2020

## Citation

> AI Analytics. FDA recall Z-2951-2020. Retrieved 2026-06-13 from https://api.ai-analytics.org/recall/Z-2951-2020. Source: US FDA. Licensed CC0.

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