Lower riskMedical device recall · FDA · Published July 30, 2026
GE Medical Systems Carescape Central Station V3 MAS800 Recall: Delay in Patient Monitoring
GE Medical Systems recalls Carescape Central Station V3 MAS800 desktop units with part numbers 5867474-04 and 5867474-13. The device may delay patient monitoring for up to 3 minutes after restart, risking missed critical health events.
Device may not resume patient monitoring for at least 3 minutes following system restart. Issue can lead to potential delay in recognition of clinically significant events.
✎ GovInfoNow plain-language explainer
GE Medical Systems is recalling certain Carescape Central Station V3 MAS800 desktop units because restarting the system can cause a delay of up to 3 minutes in patient monitoring. This delay might lead to missing critical health events if the patient's condition changes rapidly. Read more at govinfonow.com/recall/1134657-ge-medical-systems-carescape-central-station-v3-mas800-recall-delay.
“GE Medical Systems Carescape Central Station V3 MAS800 Recall: Delay in Patient Monitoring.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/1134657-ge-medical-systems-carescape-central-station-v3-mas800-recall-delay. Based on FDA recall #Z-3143-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3143-2026%22&limit=1).
The FDA announced on July 30, 2026, that GE Medical Systems Information Technologies Inc is recalling Carescape Central Station CSCS V3 MAS800 Desktop units because the device may not resume patient monitoring for at least 3 minutes following a system restart. The agency issued recall number Z-3143-2026.
How to tell if you have it
Brand: GE Medical Systems
Product: Carescape Central Station CSCS V3 MAS800 Desktop
Part Number: 5867474-04, 5867474-13
Product code: STU CSCS V3 MAI800
Integrated Part Number: 5867474-03
Product Code: STV
UDI-DI: 00195278343512 (Serial Numbers begin with STU)
UDI-DI: 00195278516367 (Serial Numbers begin with STU)
UDI-DI: 00195278343383 (Serial Numbers begin with STV)
The hazard
According to the FDA, the device may not resume patient monitoring for at least 3 minutes following a system restart. This issue can lead to a potential delay in recognition of clinically significant events.
Context
GovInfoNow's records show GE Medical Systems Information Technologies Inc has 11 other recalls on record since 2017-07-13. Other recent recalls include a 2026-07-20 recall of Portrait Core Services Software V1.0.5 for patient monitoring risk, a 2026-07-10 recall of Patient Monitor Software for unauthorized access risk, and a 2026-06-29 recall of MAC VU360 Electrocardiograph Software for data mix-up risk. Other recent recalls of similar products include Philips IntelliVue MX800 Patient Monitor Recall (2025-10-31), Philips IntelliVue MX550 Patient Monitor Recall (2025-10-31), and Philips IntelliVue MX450 Patient Monitor Recall (2025-10-31).
How to tell if you have this one
Check for part numbers 5867474-04 or 5867474-13 on the device. Units with product code STU (starting with 'STU') or serial numbers beginning with 'STV' or 'STU' are affected.
Brand
GE Medical Systems
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Device Part Number
Look for part numbers 5867474-04 or 5867474-13 on the device label.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Worldwide - US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 55 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-3143-2026 (July 30, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3143-2026 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.