# FDA recall Z-1784-2019

> **COLLINS AEROSPACE** · Class II · device recall initiated 2019-01-29.

## Product

TASE 500 Imaging systems

## Reason for recall

the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb alignment laser utilized in its TASE family of imaging systems has been miscalculated.

## Distribution

US Nationwide Distribution

## Key facts

- **Recall number:** Z-1784-2019
- **Recalling firm:** COLLINS AEROSPACE
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2019-01-29
- **Report date:** 2019-07-03

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Westford, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1784-2019

## Citation

> AI Analytics. FDA recall Z-1784-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1784-2019. Source: US FDA. Licensed CC0.

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