# FDA recall Z-2437-2021

> **Angiodynamics, Inc.** · Class II · device recall initiated 2021-07-20.

## Product

Solero Generator US PG, Item No. H78712740000US0, Catalog No. 12740000US

## Reason for recall

Specific serial numbers of the Solero MTA Generator require servicing to upgrade the software to help reduce the incidence of Error 0001, which can occur during system start-up.

## Distribution

Domestic distribution Nationwide. Foreign distribution worldwide.

## Key facts

- **Recall number:** Z-2437-2021
- **Recalling firm:** Angiodynamics, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-07-20
- **Report date:** 2021-09-15
- **Termination date:** 2023-03-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Queensbury, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2437-2021

## Citation

> AI Analytics. FDA recall Z-2437-2021. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2437-2021. Source: US FDA. Licensed CC0.

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