# FDA recall Z-2099-2019

> **Inovo, Inc** · Class II · device recall initiated 2019-04-26.

## Product

Inovo Single Luman Conserver    Product Usage:  This device is intended to regulate the flow of oxygen from an oxygen tank and only deliver oxygen as the patient inhales, resulting in greater efficiency and cost saving ratios.

## Reason for recall

The pressure gauge (manometer) may dislodge from the threaded insertion/mount, creating a leak.

## Distribution

US Nationwide Distribution - AZ, CO, FL, GA, IL, LA, MI, MO, MT, NY, SC, TX, and UT

## Key facts

- **Recall number:** Z-2099-2019
- **Recalling firm:** Inovo, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-04-26
- **Report date:** 2019-08-07
- **Termination date:** 2021-04-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lehigh Acres, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2099-2019

## Citation

> AI Analytics. FDA recall Z-2099-2019. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-2099-2019. Source: US FDA. Licensed CC0.

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