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Lower risk Medical device recall · FDA · Published September 5, 2025

AW Server 2.0

AWS

🇺🇸 FDA recall #Z-0068-2026Medical deviceAWS ›
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Contact the company

Recalling firmGE Medical Systems, SCS283 rue de la Miniere · Buc, France
✎ GovInfoNow plain-language explainer

What happened, in plain English

Source Summary by GovInfoNow · govinfonow.com/recall/51420-aws · Updated August 10, 2026 · FDA enforcement record: FDA #Z-0068-2026

Cite this page

“AW Server 2.0.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/51420-aws. Based on FDA recall #Z-0068-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0068-2026%22&limit=1).

Why it’s dangerous

AWS

Who’s affected

All

How to tell if you have this one

AWS

  • Brand
    AWS
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. 1

    AWS

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: “Domestic US distribution nationwide. International distribution worldwide.” 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 40 days after the firm started it.

1. Firm started the recall: Sep 5, 202512. FDA classified it Class II: Oct 8, 202523. Published in FDA’s Enforcement Report: Oct 15, 202532025
  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-0068-2026 (September 5, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0068-2026 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