# FDA recall Z-2340-2018

> **GE Healthcare Finland Oy** · Class II · device recall initiated 2018-05-25.

## Product

GE Healthcare CARESCAPE Monitor B650

## Reason for recall

When multiple CARESCAPE Monitor B650 units are connected to the same network and a network overload occurs for a prolonged time, the monitors may simultaneously restart as designed.  The monitor restart will not be completed until the network issue has been corrected.

## Distribution

worldwide

## Key facts

- **Recall number:** Z-2340-2018
- **Recalling firm:** GE Healthcare Finland Oy
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2018-05-25
- **Report date:** 2018-07-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Helsinki, Finland

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2340-2018

## Citation

> AI Analytics. FDA recall Z-2340-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2340-2018. Source: US FDA. Licensed CC0.

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