Use caution Medical device recall · FDA · Published April 20, 2026

GE Medical Systems Allia IGS 3 Pulse X-Ray System Recall: Electrical Shock Risk

GE Medical Systems recalls Allia IGS 3 Pulse angiographic X-ray systems with potential electrical shock risk during installation or maintenance. 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-2314-2026Medical device GE Medical Systems ›

Use caution until it’s fixed

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.

Take action

Contact the company

Recalling firmGE Medical Systems, LLC3000 N Grandview Blvd · Waukesha, WI 53188-1615

✎ GovInfoNow plain-language explainer

GE Medical Systems is recalling certain Allia IGS 3 Pulse angiographic X-ray systems due to a potential electrical cable issue that could cause shock to service personnel during maintenance. This recall affects specific units with known serial numbers and UDI-DI codes. Read more at govinfonow.com/recall/49452-ge-medical-systems-allia-igs-3-pulse-x-ray-system.

Source Summary by GovInfoNow · govinfonow.com/recall/49452-ge-medical-systems-allia-igs-3-pulse-x-ray-system · Updated August 10, 2026 · FDA enforcement record: FDA #Z-2314-2026

Cite this page

“GE Medical Systems Allia IGS 3 Pulse X-Ray System Recall: Electrical Shock Risk.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/49452-ge-medical-systems-allia-igs-3-pulse-x-ray-system. Based on FDA recall #Z-2314-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2314-2026%22&limit=1).

The FDA announced on April 20, 2026, that GE Medical Systems, LLC is recalling the Allia IGS 3 Pulse angiographic X-ray system due to a potential electrical shock hazard. Owners should contact the company for remedy details.

How to tell if you have it

Brand: GE Medical Systems
Product: Allia IGS 3 Pulse angiographic X-ray system
UDI-DI: 00195278719577
Serial Numbers: M3-24-053, M3-24-124, M3-25-029, M3-25-051, M3-25-053, M3-25-091, M3-25-098, M3-25-124, M3-26-010, M3-26-030

The hazard

The recall addresses a potential issue with an electrical cable on certain IGS systems equipped with Gaia generators. This defect could cause a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.

Context

GovInfoNow's records show GE Medical Systems, LLC has 27 other recalls on record since March 30, 2018. Recent similar recalls include the GE Optima XR220amx Mobile X-Ray System Recall (June 5, 2026), the GE Medical Systems Giraffe OmniBed FRU Recall (May 1, 2026), and the GE Medical Systems Revolution Apex Plus CT Scanner Security Vulnerability Recall (March 26, 2026). Other recent recalls of similar products include the GE Maxxus Nuclear Medicine Systems Recall (Dec. 10, 2025), the GE HealthCare Telemetry Server Recall (April 24, 2026), and the Philips Allura Xper FD10C Medical System Recall (Dec. 15, 2025).

How to tell if you have this one

Check for serial numbers starting with M3-24- or M3-25- or M3-26- in the list provided. The UDI-DI code 00195278719577 also identifies affected units.

Brand
GE Medical Systems
Category
Medical device

FDA recall event · 5 products

All 5 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 - US Nationwide distribution.

Recall number	Product, codes & lots	Quantity
Z-2314-2026	Allia IGS 3 Pulse angiographic X-ray system; UDI-DI: 00195278719577; Serial Numbers: M3-24-053, M3-24-124, M3-25-029, M3-25-051, M3-25-053, M3-25-091, M3-25-098, M3-25-124, M3-26-010, M3-26-030	9 units
Z-2315-2026	Allia IGS 5 Pulse angiographic X-ray system; UDI-DI: 00195278719263; Serial Numbers: M2-23-039, M2-23-056, M2-24-004, M2-24-019, M2-24-020, M2-24-025, M2-24-030, M2-24-031, M2-24-032, M2-24-033, M2-24-034, M2-24-037, M2-24-038, M2-24-039, M2-24-040, M2-24-046, M2-24-057, M2-24-062, M2-24-064, M2-24-066, M2-24-069, M2-24-071, M2-24-077, M2-24-078, M2-24-080, M2-24-083, M2-25-003, M2-25-004, M2-25-005, M2-25-011, M2-25-013, M2-25-015, M2-25-017, M2-25-019, M2-25-023, M2-25-024, M2-25-025, M2-25-026, M2-25-028, M2-25-032, M2-25-036, M2-25-037, M2-25-039, M2-25-040, M2-25-041, M2-25-042, M2-25-043, M2-25-046, M2-25-048, M2-25-049, M2-25-056, M2-25-057, M2-25-058, M2-25-062, M2-25-065, M2-25-067, M2-25-072, M2-25-074, M2-25-077, M2-25-078, M2-25-080, M2-25-250, M2-25-300, M2-26-002, M2-26-004, M2-26-006, M2-26-007, M2-UP2502, M3-22-012, M3-23-117, M3-24-019, M3-24-021, M3-24-023, M3-24-034, M3-24-052, M3-24-061, M3-24-074, M3-24-079, M3-24-086, M3-24-090, M3-24-094, M3-24-095, M3-24-097, M3-24-099, M3-24-101, M3-24-104, M3-24-111, M3-24-120, M3-24-128, M3-24-136, M3-24-137, M3-24-141, M3-24-143, M3-24-149, M3-24-151, M3-24-156, M3-24-159, M3-24-161, M3-24-163, M3-24-165, M3-24-168, M3-24-169, M3-24-172, M3-24-175, M3-25-003, M3-25-012, M3-25-017, M3-25-020, M3-25-027, M3-25-036, M3-25-061, M3-25-063, M3-25-069, M3-25-074, M3-25-076, M3-25-079, M3-25-080, M3-25-084, M3-25-085, M3-25-088, M3-25-089, M3-25-094, M3-25-104, M3-25-106, M3-25-107, M3-25-115, M3-25-118, M3-25-119, M3-25-120, M3-25-128, M3-25-130, M3-25-132, M3-25-145, M3-25-147, M3-25-148, M3-25-149, M3-25-150, M3-25-151, M3-26-002, M3-26-003, M3-26-005, M3-26-007, M3-26-021, M3-26-024, M3-26-027, M3-26-028, M3-26-033, M3-26-034, M3-UP2501, M3-UP2503	121 units
Z-2316-2026	Allia IGS 7 Pulse angiographic X-ray system; UDI-DI: 00195278719720; Serial Numbers: D3-23-024, D3-23-029, D3-24-001, D3-24-002, D3-24-005, D3-24-006, D3-24-008, D3-24-009, D3-24-010, D3-24-013, D3-24-014, D3-24-016, D3-24-019, D3-24-020, D3-24-021, D3-24-023, D3-24-025, D3-25-001, D3-25-002, D3-25-003, D3-25-005, D3-25-006, D3-25-007, D3-25-008, D3-25-009, D3-25-010, D3-25-013, D3-25-016, D3-25-017, D3-25-018, D3-25-026, D3-25-027, D3-25-029, D3-25-030, D3-25-034, D3-25-036, D3-25-037, D3-26-001, D3-26-002, D3-26-007	35 units
Z-2317-2026	Allia IGS Pulse angiographic X-ray system; UDI-DI: 00195278827647; Serial Numbers: DVMSS2500001HL, DVMSS2500002HL, DVMSS2500003HL, DVMSS2500004HL, DVMSS2500005HL, DVMSS2500006HL, DVMSS2600001HL, DVMSS2600002HL	5 units
Z-2318-2026	Allia Moveo angiographic X-ray system; UDI-DI: 00198953052488; Serial Numbers: C4-25-001, C4-25-002, C4-26-001, C4-26-002, C4-26-004, C4-26-005	3 units

Based on the official FDA remedy

What to do — step by step

Stop Using for Maintenance
Do not perform installation, maintenance, or troubleshooting inside the C-FRT cabinet while the system is powered on.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

FDA distribution: “Worldwide - US Nationwide distribution.” 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 58 days after the firm started it.

Apr 20, 2026Firm started the recall
Jun 5, 2026FDA classified it Class II
Jun 17, 2026Published in FDA’s Enforcement Report

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

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

Which units are affected?

Units with serial numbers M3-24-053, M3-24-124, M3-25-029, M3-25-051, M3-25-053, M3-25-091, M3-25-098, M3-25-124, M3-26-010, M3-26-030 and UDI-DI 00195278719577.

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Link to this recall

<a href="https://govinfonow.com/recall/49452-ge-medical-systems-allia-igs-3-pulse-x-ray-system">GE Medical Systems Allia IGS 3 Pulse X-Ray System Recall: Electrical Shock Risk (GovInfoNow)</a>

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-2314-2026 (April 20, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2314-2026 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.