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Use caution Medical device recall · FDA · Published May 10, 2022

GE Healthcare CARESCAPE Central Station V2: Power Supply Failure Risk

GE Healthcare recalls CARESCAPE Central Station V2 models 2082278-001 and 2082279-001 due to potential power supply failure causing loss of patient monitoring. Affected units include specific display and component parts.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-1265-2022Medical deviceGE Healthcare ›
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Contact the company

Recalling firmGE Healthcare, LLC3000 N Grandview Blvd · Waukesha, WI 53188-1615
✎ GovInfoNow plain-language explainer

GE Healthcare is recalling certain CARESCAPE Central Station V2 medical devices because a power supply component failure could shut down the system, leading to loss of patient monitoring. This affects specific model numbers and related display components. Read more at govinfonow.com/recall/60709-ge-healthcare-carescape-central-station-v2-power-supply-failure-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/60709-ge-healthcare-carescape-central-station-v2-power-supply-failure-risk · Updated August 10, 2026 · FDA enforcement record: FDA #Z-1265-2022

Cite this page

“GE Healthcare CARESCAPE Central Station V2: Power Supply Failure Risk.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/60709-ge-healthcare-carescape-central-station-v2-power-supply-failure-risk. Based on FDA recall #Z-1265-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1265-2022%22&limit=1).

The FDA announced on May 10, 2022, that GE Healthcare LLC is recalling CARESCAPE Central Station (CSCS) V2 units due to a potential power supply component failure. This defect can cause the device to shut down, leading to loss of patient monitoring at the central station.

How to tell if you have it

  • GE Healthcare CARESCAPE Central Station (CSCS) V2, Model numbers 2082278-001 and 2082279-001
  • Part #2082294-001, FRU MP200 POWER SUPPLY ASSEMBLY
  • Part #2082293-002-R, FRU MP200 CPU ASSEMBLY
  • Part #2082293-002, FRU MP200 CPU ASSEMBLY
  • Part #2071523-001, MP200 22 IN DISPLAY WITH TOUCH
  • Part #2092930-001, DSP LCD 22 IN MED W/TCH W/DKST N AMR
  • Part #2092930-002, DSP LCD 22 IN MED W/TCH W/DKST BRIT P/C
  • Part #2092930-003, DSP LCD 22IN MED W/TCH W/DKST EURO P/C
  • Part #2092930-004, DSP LCD 22IN MED W/TCH W/DKST ITA P/C
  • Part #2092930-005, DSP LCD 22IN MED W/TCH W/DKST INDIAN P/C
  • Part #2092930-006, DSP LCD 22IN MED W/TCH W/DKST ISREAL P/C
  • Part #2092930-007, DSP LCD 22IN MED W/TCH W/DKST SWISS P/C
  • Part #2092930-008, DSP LCD 22IN MED W/TCH W/DKST AUSTRL P/C
  • Part #2092930-009, DSP LCD 22IN MED W/TCH W/DKST JPN
  • Part #2092930-010, DSP LCD 22IN MED W/TCH W/DKST BRZL P/C
  • Part #2092930-011, DSP LCD 22IN MED W/TCH W DKST ARGNT P C
  • Part #2092930-012, DSP LCD 22IN MED W TCH W DKST DENMARK
  • Part #2092930-013, DSP LCD22IN MED W TCH W DKST S AFRICA P C
  • Part #2092930-014, DSP LCD22IN MED W TCH W DKST CHINA P C
  • CSCS V2 MA1700 Integrated, Product Code SKN, Model #2082278-001, GTIN 00840682109666
  • CSCS V2 MAS700 Desktop, Product Code SNF, Model #2082279-001, GTIN 00840682109604

The hazard

The CARESCAPE Central Station (CSCS) V2 can shut down due to a potential power supply component failure. This can lead to loss of patient monitoring at the central station.

Context

GovInfoNow's records show GE Healthcare LLC has 97 other recalls on record since 2017-10-04. Other recent recalls include GE Healthcare SIGNA Premier MRI Scanners May Have Steel Fittings Risking Injury (2026-02-27), GE Centricity Universal Viewer 6.0/7.0/8.0: Inaccurate Distance Measurements (2022-07-15), and GE Healthcare SIGNA Premier MRI Scanner Recall: Risk of Hearing Loss from Acoustic Noise (2022-06-24). Other recent recalls of similar products include GE HealthCare CARESCAPE Telemetry Server V5 Recall: Risk of ECG/SpO2 Monitoring Loss (2026-04-24), GE Healthcare Carestation Anesthesia Systems May Shut Down During Power Loss (2025-11-14), and GE HealthCare Telemetry Server Recall: Risk of ECG/SpO2 Monitoring Loss (2026-04-24).

How to tell if you have this one

Check for model numbers 2082278-001 or 2082279-001 on the device. Affected units also include specific display parts with part numbers starting with 2092930.

  • Brand
    GE Healthcare
  • Product
    GE Healthcare, LLC recalls CARESCAPE Central Station (CSCS) V2, Model numbers 2082278-001 and 2082279-001. Update 3/10/2023: The following FRU and
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Device Model

    Identify the model number on the device label to confirm if it is 2082278-001 or 2082279-001.

  2. Contact Manufacturer

    Reach out to GE Healthcare for guidance on affected components and next steps.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Worldwide distribution - US Nationwide. There was also military/government distribution and the countries of Algeria, Argentina, Australia, Austria, Bahamas, Bahrain, Bangladesh, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Bulgaria,…” 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 43 days after the firm started it.

1. Firm started the recall: May 10, 202212. FDA classified it Class II: Jun 13, 202223. Published in FDA’s Enforcement Report: Jun 22, 202232022
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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-1265-2022 (May 10, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1265-2022 to see it in context.
  • Plain-language summary written by qwen3:4b on August 10, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA