# FDA recall Z-1285-2022

> **GE Healthcare, LLC** · Class II · device recall initiated 2022-04-25.

## Product

Back up batteries in Avance CS2 and Avance CS2 Pro anesthesia devices manufactured  on or after April 1, 2019

## Reason for recall

Backup batteries can fail earlier than their estimated life.

## Distribution

Worldwide distribution - US Nationwide and the countries of Algeria, Australia, Austria, Bangladesh, Belgium, Brazil, China, Columbia, Costa Rica, Cyprus, Czech Republic, Denmark, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iraq, Italy, Japan, Kazakhstan, Kenya, Korea, Kuwait, Lao PDR, Latvia, Lebanon, Libya, Lithuania, Macedonia, Malaysia, Mexico, Morocco, Nepal, New Zealand, Norway, Oman, Panama, Peru, Philippines, Poland, Portugal, Romania, Russia, Saudi Arabia, Singapore, Slovakia, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, Ukraine, United Arab Emirates, United Kingdom, and Vietnam.

## Key facts

- **Recall number:** Z-1285-2022
- **Recalling firm:** GE Healthcare, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-04-25
- **Report date:** 2022-07-06

- **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-1285-2022

## Citation

> AI Analytics. FDA recall Z-1285-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1285-2022. Source: US FDA. Licensed CC0.

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