# FDA recall Z-2703-2017

> **GE Healthcare, LLC** · Class II · device recall initiated 2017-05-02.

## Product

Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1

## Reason for recall

Carestation 620, 650 and 650c has Potential for Elevated FiCO2 and Unexpected System Malfunction

## Distribution

US Distribution including PR and to the states of :  AL, AR, AZ, CA, CO, CT, FL GA, ID,IL, IN, KY, LA, , MA, MD, MI, MO, MS, MT,  MN, NC, NH, NJ, NV, NY, OH, OK, PA, TN, TX,  VA, WA, WI, and UT.      OUS:     Algeria  Argentina  Australia  Austria  Belgium  Bolivia  Bosnia and Herzegovina  Brazil  Bulgaria  Cambodia  Canada  Chile  Colombia  Costa Rica  Cote d'Ivoire  Croatia  Czech Republic  Ecuador  Egypt  El Salvador  Estonia  Finland  France  Germany  Greece  Honduras  Hong Kong  Hungary  India  Indonesia  Iraq  Ireland  Israel  Italy  Japan  Jordan  Kenya  Korea (Republic Of)  Kuwait  Latvia  Lebanon  Lithuania  Malaysia  Maldives  Malta  Mauritius  Mexico  Moldova  Morocco  Myanmar  Netherlands  New Zealand    Nigeria  Norway  Oman  Pakistan  Paraguay  Peru  Philippines  Poland  Portugal  Romania  Russia  Saudi Arabia  Senegal  Serbia  Singapore  Slovakia  Slovenia  South Africa  Spain  Sweden  Switzerland  Taiwan  Tanzania  Thailand  Turkey  United Arab Emirates  United Kingdom 

## Key facts

- **Recall number:** Z-2703-2017
- **Recalling firm:** GE Healthcare, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-02
- **Report date:** 2017-07-19
- **Termination date:** 2018-02-13

- **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-2703-2017

## Citation

> AI Analytics. FDA recall Z-2703-2017. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2703-2017. Source: US FDA. Licensed CC0.

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