# FDA recall Z-0897-2018

> **Boston Scientific Corporation** · Class II · device recall initiated 2017-09-22.

## Product

Auriga 30 Laser System, Universal Part Number: M0068S30G0.    Intended to be used in surgical procedures.

## Reason for recall

Certain Auriga consoles have incorrectly assembled trigger wire components. The trigger wire functions in the start-up of the console. An incorrectly assembled trigger wire may result in error codes or failure to start the console.

## Distribution

International Distribution Only -- Australia, Vietnam, France, Germany, Italy, Spain, and Romania.

## Key facts

- **Recall number:** Z-0897-2018
- **Recalling firm:** Boston Scientific Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-09-22
- **Report date:** 2018-03-14
- **Termination date:** 2018-08-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Marlborough, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0897-2018

## Citation

> AI Analytics. FDA recall Z-0897-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0897-2018. Source: US FDA. Licensed CC0.

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