# FDA recall Z-1427-2022

> **GE Healthcare, LLC** · Class II · device recall initiated 2022-05-27.

## Product

GE Healthcare Avance CS2, Avance CS2 Pro Anesthesia Systems, Part #1009-9050-000; and Aisys CS2 Anesthesia Systems, Part # 1011-9050-000.

## Reason for recall

The base of the anesthesia system can have a crack and could potentially fracture resulting in a tip or overbalance of the anesthesia system.  This can result in potential injury if it falls on a person.

## Distribution

Distribution was made to AZ, CA, CO, CT, FL, IA, ID, IL, IN, KY, LA, MA, MD, ME, MI, MO, MT, NC, NE, NV, NY, OH, PA, SC, TN, TX, VA, and WV.  There was also military distribution but no government distribution.    Foreign distribution was made to Australia, Canada, China, Estonia, Finland, France, Germany, Greece, India, Indonesia, Iraq, Ireland, Italy, Japan, Jordan, Kenya, Korea, Malaysia, New Zealand, Philippines, Romania, Russia, Saudi Arabia, Switzerland, Taiwan, Turkey, United Arab Emirates, United Kingdom, and Vietnam.

## Key facts

- **Recall number:** Z-1427-2022
- **Recalling firm:** GE Healthcare, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-05-27
- **Report date:** 2022-07-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukesha, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1427-2022

## Citation

> AI Analytics. FDA recall Z-1427-2022. Retrieved 2026-07-09 from https://api.ai-analytics.org/recall/Z-1427-2022. Source: US FDA. Licensed CC0.

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