# FDA recall Z-0820-2022

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2022-02-14.

## Product

Compella Bariatric Bed System

## Reason for recall

Potential damage to the power cord may cause the power conductors to be exposed, thereby creating a risk of shock from the power mains.

## Distribution

Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bahamas, Bahrain, Belgium, Bermuda, Brazil, Cameroon, Canada, Estonia, Finland, France, Georgia, Germany, Greece, Hungary, India, Ireland, Italy, Jamaica, Jordan, Kuwait, Mexico, Netherlands, New Zealand, Norway, Oman, Poland, Qatar, Romania, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, Thailand, Turkmenistan, UAE, and UK.

## Key facts

- **Recall number:** Z-0820-2022
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-02-14
- **Report date:** 2022-03-30

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0820-2022

## Citation

> AI Analytics. FDA recall Z-0820-2022. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0820-2022. Source: US FDA. Licensed CC0.

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