Fresh Recalls

FDAClass II · Medical device · Recall Z-3143-2026 · Recalled September 23, 2026

Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04 recall — GE Medical Systems Information Technologies Inc

Agency report date: September 23, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04
Company / brand
GE Medical Systems Information Technologies
Lot / serial / date codes
5867474-04 UDI-DI 00195278343512 Device Serial Numbers begin with STU 5867474-13 UDI-DI 00195278516367 Device Serial Numbers begin with STU 5867474-03 UDI-DI 00195278343383 Device Serial Numbers begin with STV
Distribution
Worldwide - US Nationwide distribution.
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04 recall status

3. Open the official notice or contact

Official recall ID
Z-3143-2026
Brand
All GE Medical Systems Information Technologies recalls
Classification
Class II
Units affected
29,570 (23,632 US; 5,938 OUS)
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Waukesha, WI, United States
Firm address
3114 N Grandview Blvd, N/A, 53188-1615

Identifying details (verbatim from the notice)

Product codes / lots
5867474-04 UDI-DI 00195278343512 Device Serial Numbers begin with STU 5867474-13 UDI-DI 00195278516367 Device Serial Numbers begin with STU 5867474-03 UDI-DI 00195278343383 Device Serial Numbers begin with STV
Distribution
Worldwide - US Nationwide distribution.
Firm notified the public via
Letter
FDA event ID
99637
Recall initiated
July 30, 2026
FDA classified
September 11, 2026
FDA report date
September 23, 2026

Other medical device recalls from around the same time

Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved October 22, 2026 at 6:00 PM UTC.

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