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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Monitoring Devices

GE HealthCare Carescape Central Stations Recalled for Reboot Issue

Agency Publication Date: October 21, 2025
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Summary

Wipro GE Healthcare is recalling approximately 2,479 Carescape Central Station (CSCS) V3 MAS800 Desktop units due to a software defect in version V3.0.5. The affected central stations can enter a continuous reboot cycle when exactly 118, 119, or 120 stations are connected to the same network at once. If the system reboots repeatedly, it results in a total loss of central monitoring for all patients connected to that station. GE HealthCare is notifying affected clinical facilities via letter to implement corrective actions.

Risk

The continuous rebooting prevents medical staff from seeing critical patient data and alarms at the central monitoring station. This delay in monitoring could prevent timely intervention during life-threatening medical events.

What You Should Do

  1. This recall affects GE Healthcare Carescape Central Station (CSCS) V3 MAS800 Desktop units with software version V3.0.5, specifically Part Numbers 5867474-04 and 5867474-03.
  2. Identify if your device is affected by checking the model, software version, part number, and serial number. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled devices if your facility network has between 118 and 120 central stations connected, as this specific configuration triggers the rebooting failure.
  4. Clinical staff should transition patients to alternative monitoring solutions if the central station becomes unavailable.
  5. Contact GE HealthCare or your local distributor to arrange for necessary software corrections or updates.
  6. Call the FDA: 1-888-463-6332 (1-888-INFO-FDA) for additional information regarding medical device safety and recalls.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: GE Healthcare Carescape Central Station (CSCS) V3 MAS800 Desktop (Software V3.0.5)
Variants: Desktop, Cathode ray tube display
Model / REF:
5867474-04
Serial Numbers (173):
STU25210418SA
STU25210417SA
STU25210419SA
STU25250440SA
STU25250439SA
STU25260447SA
STU25210407SA
STU25210406SA
STU24200003SA
STU24200006SA
STU24200005SA
STU24200004SA
STU23240015SA
STU24240019SA
STU24240020SA
STU24240007SA
STU24240022SA
STU24240021SA
STU24330020SA
STU24240014SA
STU24240013SA
STU24330019SA
STU24330022SA
STU24330016SA
STU24240005SA
STU24240008SA
STU24240012SA
STU24330018SA
STU24330021SA
STU24330017SA
STU23160011SA
STU23240007SA
STU24310001SA
STU25210433SA
STU25210432SA
STU25200390SA
STU25200392SA
STU25200391SA
STU25200399SA
STU25200397SA
STU25200395SA
STU25200393SA
STU25200398SA
STU25200396SA
STU25250438SA
STU25270475SA
STU25270456SA
STU25270468SA
STU25270458SA
STU25270466SA
GTIN:
00195278343512
Product: GE Healthcare Carescape Central Station (CSCS) V3 MAS800 Desktop (Software V3.0.5)
Variants: Desktop, Cathode ray tube display
Model / REF:
5867474-03
Serial Numbers (2305):
STV25225456SA
STV25225455SA
STV25266464SA
STV25235817SA
STV25235816SA
STV25286682SA
STV25225594SA
STV25235792SA
STV25235774SA
STV25225550SA
STV25235626SA
STV25235625SA
STV25184592SA
STV25235628SA
STV25235631SA
STV25184595SA
STV25235629SA
STV25235632SA
STV25235630SA
STV25276515SA
STV25225510SA
STV25276516SA
STV25225505SA
STV25225508SA
STV25225509SA
STV25225507SA
STV25225506SA
STV25113369SA
STV25204986SA
STV25205160SA
STV25205151SA
STV25205161SA
STV25062736SA
STV25256133SA
STV25225512SA
STV25296702SA
STV25296701SA
STV25296748SA
STV25256214SA
STV25225511SA
STV25256215SA
STV25256199SA
STV25256216SA
STV25256202SA
STV25225497SA
STV25225514SA
STV25225498SA
STV25256131SA
STV25256129SA
STV25256128SA
GTIN:
00195278343383

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97646
Status: Active
Manufacturer: Wipro GE Healthcare Private Ltd.
Sold By: Authorized medical device distributors; Direct medical sales
Manufactured In: India
Units Affected: 2 products (173 units; 2306 units)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.