# FDA recall Z-0482-2022

> **Ohio Medical Corporation** · Class II · device recall initiated 2021-11-16.

## Product

Instavac Portable Suction Pump, Constant mode (model #757000, Instavac C) and Intermittent mode (model 756000, Instavac I); and Instavac replacement pumps, part #AI5511, a component of model numbers 756000 and 757000.

## Reason for recall

Increase in premature device failures

## Distribution

US Nationwide, including PR.  There was government and foreign distribution.  There was no military distribution.

## Key facts

- **Recall number:** Z-0482-2022
- **Recalling firm:** Ohio Medical Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-11-16
- **Report date:** 2022-01-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Gurnee, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0482-2022

## Citation

> AI Analytics. FDA recall Z-0482-2022. Retrieved 2026-07-08 from https://api.ai-analytics.org/recall/Z-0482-2022. Source: US FDA. Licensed CC0.

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