# FDA recall Z-1786-2019

> **Monarch Medical Technologies** · Class II · device recall initiated 2019-05-03.

## Product

Monarch Medical Technologies EndoTool IV, Versions 1.8, Version 1.8.5 and higher, and Version 1.9 and Version 1.10.

## Reason for recall

Insulin dosing calculations were erroneously high.

## Distribution

Nationwide and Dubai

## Key facts

- **Recall number:** Z-1786-2019
- **Recalling firm:** Monarch Medical Technologies
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2019-05-03
- **Report date:** 2019-06-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Charlotte, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1786-2019

## Citation

> AI Analytics. FDA recall Z-1786-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1786-2019. Source: US FDA. Licensed CC0.

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