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Use caution Medical device recall · FDA · Published April 11, 2024

FUJIFILM Noblus AC Adapter Recall: Risk of Smoke from Power Cable Stress

FUJIFILM Healthcare recalls Noblus AC adapters for ultrasound systems that may overheat and cause smoke if power cables are frequently plugged in and out.

🇺🇸 FDA recall #Z-1884-2024Medical deviceFUJIFILM Healthcare ›
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Recalling firmFUJIFILM Healthcare Americas Corporation81 Hartwell Ave Ste 300 · Lexington, MA 02421-3160
✎ GovInfoNow plain-language explainer

What happened, in plain English

FUJIFILM Healthcare is recalling Noblus AC adapters used with the Noblus Ultrasound Imaging System Model AHM250PS24. The adapters can heat up and cause smoke if the power cable is frequently inserted or removed, which could lead to fire or injury. Read more at govinfonow.com/recall/55413-fujifilm-noblus-ac-adapter-recall-risk-of-smoke-from-power.

Source Summary by GovInfoNow · govinfonow.com/recall/55413-fujifilm-noblus-ac-adapter-recall-risk-of-smoke-from-power · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1884-2024

Cite this page

“FUJIFILM Noblus AC Adapter Recall: Risk of Smoke from Power Cable Stress.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/55413-fujifilm-noblus-ac-adapter-recall-risk-of-smoke-from-power. Based on FDA recall #Z-1884-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1884-2024%22&limit=1).

Why it’s dangerous

The AC adapters can overheat and produce smoke when the power cable is subjected to frequent insertion or removal. This mechanical stress can cause the adapter to fail, potentially leading to fire or injury.

Who’s affected

Users of the Noblus Ultrasound Imaging System Model AHM250PS24 with the specified AC adapters are affected. Medical professionals using these systems are most at risk due to potential fire or injury from overheating.

How to tell if you have this one

Check for the Noblus Ultrasound Imaging System Model AHM250PS24 with AC adapters having a serial number before K17160001 (excluding K17160001). The UDI-DI number is (01) 04580292771704.

  • Brand
    FUJIFILM Healthcare
  • Product
    Noblus AC Adapter used with the Noblus Ultrasound Imaging System Model : AHM250PS24
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Adapter Serial Number

    Look for the serial number on the adapter, which should be before K17160001 (excluding K17160001).

Where it went and when

Where it was distributed

Distributed nationwide.

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: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 48 days after the firm started it.

1. Firm started the recall: Apr 11, 202412. FDA classified it Class II: May 22, 202423. Published in FDA’s Enforcement Report: May 29, 202432024
  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-1884-2024 (April 11, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1884-2024 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 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