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Use caution Medical device recall · FDA · Published March 18, 2024

GE Healthcare Allia IGS 7 OR X-ray Systems Recall: Risk of Gantry Fall

GE Healthcare recalls Allia IGS 7 OR x-ray systems due to potential bolt adhesive issues that could cause detector or X-ray tube falls. Affected units have specific serial numbers and UDI/DI codes.

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

🇺🇸 FDA recall #Z-1781-2024Medical deviceGE Healthcare ›
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Contact the company

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

GE Healthcare is recalling Allia IGS 7 OR x-ray systems because some bolts may not have proper adhesive, which could cause the detector or X-ray tube to fall. This poses a risk of injury to users during medical procedures. Read more at govinfonow.com/recall/55849-ge-healthcare-allia-igs-7-or-x-ray-systems-recall.

Source Summary by GovInfoNow · govinfonow.com/recall/55849-ge-healthcare-allia-igs-7-or-x-ray-systems-recall · Updated August 17, 2026 · FDA enforcement record: FDA #Z-1781-2024

Cite this page

“GE Healthcare Allia IGS 7 OR X-ray Systems Recall: Risk of Gantry Fall.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/55849-ge-healthcare-allia-igs-7-or-x-ray-systems-recall. Based on FDA recall #Z-1781-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1781-2024%22&limit=1).

The FDA announced on March 18, 2024, that GE Healthcare is recalling two units of the Allia IGS 7 OR interventional fluoroscopic x-ray systems due to a potential fall hazard. The agency issued recall number Z-1781-2024 for the Class II voluntary recall.

How to tell if you have it

  • Brand: GE Healthcare
  • Product: Allia IGS 7 OR, Interventional fluoroscopic x-ray systems
  • UDI/DI: 00195278215550
  • Serial Numbers: D3-23-026, D4-24-002
  • Quantity: 2 units

The hazard

GE Healthcare stated that adhesive material might not have been applied to some bolts of certain Innova IGS, Discovery IGS, Interact IGS, Allia IGS and Allia Pulse IGS products. This defect could result in a potential fall of the Detector/Elevator or X-ray tube of the frontal Gantry assembly.

Context

GovInfoNow's records show GE Medical Systems SCS has four other recalls on record since March 29, 2018. Other recent recalls include the GE Healthcare AW Server 3.2 ext.6.5 recall dated May 8, 2026, and the AWS security vulnerability recall dated September 5, 2025. Similar product recalls include the GE Maxxus Nuclear Medicine Systems recall on December 10, 2025, and the GE Medical Systems Allia IGS 3 Pulse and Allia IGS 7 Pulse X-Ray System recalls on April 20, 2026.

How to tell if you have this one

Check for serial numbers D3-23-026 or D4-24-002 and UDI/DI code 00195278215550 on the equipment. These specific models are affected by the recall.

  • Brand
    GE Healthcare
  • Category
    Medical device
FDA recall event · 7 products

All 7 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    Worldwide distribution - US Nationwide in the states of CA, FL, GA, IN, MA, NC, OK, SC, TN, TX, VA and the countries of Armenia, China, France, Hungary, India, Italy, Japan, Kazakhstan, Lithuania, Mexico, Russia, Spain, Taiwan, Turkey, Vietnam
Recall numberProduct, codes & lotsQuantity
Z-1777-2024GE Healthcare Innova IGS 5, computed tomography x-ray system; UDI/DI 00840682124621, Serial Numbers: M2-23-042, M2-23-046, M2-23-048, M2-23-051, M2-24-001, M3-23-097, M3-23-098, M3-23-106, M3-23-108, M3-23-109, M3-23-111, M3-23-112, M3-23-114, M3-23-116, M3-23-123, M4-23-046, M4-23-053, M4-23-054, M4-23-055, M4-23-056, M4-24-00121 units
Z-1778-2024GE Healthcare Innova IGS 6, Interventional fluoroscopic x-ray systems; UDI/DI 00840682124614, Serial Numbers: B3-23-015, B3-23-016, B3-24-002;3 units
Z-1779-2024GE Healthcare Interact Discovery RT, Interventional fluoroscopic x-ray systems; UDI/DI 00840682141581, Serial Numbers: M4-23-0491 unit
Z-1780-2024GE Healthcare Allia IGS 7, Interventional fluoroscopic x-ray systems; UDI/DI 00195278215543, Serial Numbers: D4-23-035, D4-23-036, D4-23-038, D4-23-042, D4-24-001, D4-24-0036 units
Z-1781-2024GE Healthcare Allia IGS 7 OR, Interventional fluoroscopic x-ray systems; UDI/DI 00195278215550, Serial Numbers: D3-23-026, D4-24-0022 units
Z-1782-2024GE Healthcare Allia IGS 5 Pulse, Interventional fluoroscopic x-ray systems; UDI/DI 00195278719263, Serial Numbers: M3-23-1171 unit
Z-1783-2024GE Healthcare Allia IGS 5 Pulse, Interventional fluoroscopic x-ray systems; UDI/DI 00195278719263, Serial Numbers: M3-23-1171 unit
Based on the official FDA remedy

What to do — step by step

  1. Check Equipment Serial Numbers

    Look for serial numbers D3-23-026 or D4-24-002 on the Allia IGS 7 OR x-ray systems.

Where it went and when

Where it was distributed

Distributed nationwide and abroad; the notice names 11 states.

Alaska: nationwideAKMaine: nationwideMEVermont: nationwideVTNew Hampshire: nationwideNHWashington: nationwideWAIdaho: nationwideIDMontana: nationwideMTNorth Dakota: nationwideNDMinnesota: nationwideMNIllinois: nationwideILWisconsin: nationwideWIMichigan: nationwideMINew York: nationwideNYRhode Island: nationwideRIMassachusetts: named in the noticeMAOregon: nationwideORNevada: nationwideNVWyoming: nationwideWYSouth Dakota: nationwideSDIowa: nationwideIAIndiana: named in the noticeINOhio: nationwideOHPennsylvania: nationwidePANew Jersey: nationwideNJConnecticut: nationwideCTCalifornia: named in the noticeCAUtah: nationwideUTColorado: nationwideCONebraska: nationwideNEMissouri: nationwideMOKentucky: nationwideKYWest Virginia: nationwideWVVirginia: named in the noticeVAMaryland: nationwideMDDelaware: nationwideDEArizona: nationwideAZNew Mexico: nationwideNMKansas: nationwideKSArkansas: nationwideARTennessee: named in the noticeTNNorth Carolina: named in the noticeNCSouth Carolina: named in the noticeSCDistrict of Columbia: nationwideDCOklahoma: named in the noticeOKLouisiana: nationwideLAMississippi: nationwideMSAlabama: nationwideALGeorgia: named in the noticeGAHawaii: nationwideHITexas: named in the noticeTXFlorida: named in the noticeFL

FDA distribution: “Worldwide distribution - US Nationwide in the states of CA, FL, GA, IN, MA, NC, OK, SC, TN, TX, VA and the countries of Armenia, China, France, Hungary, India, Italy, Japan, Kazakhstan, Lithuania, Mexico, Russia, Spain, Taiwan, Turkey,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: California, Florida, Georgia, Indiana, Massachusetts, North Carolina, Oklahoma, South Carolina, Tennessee, Texas, Virginia.

Recall timeline

FDA published this recall 58 days after the firm started it.

1. Firm started the recall: Mar 18, 202412. FDA classified it Class II: May 6, 202423. Published in FDA’s Enforcement Report: May 15, 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-1781-2024 (March 18, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1781-2024 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 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