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.
GE HealthCare has become aware of the potential 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 could result in a potential fall of the Detector/Elevator or X-ray tube of the frontal Gantry assembly.
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.
The adhesive on certain bolts might not be properly applied, which could cause the detector or X:ray tube to fall. This fall could injure medical staff or patients during procedures.
Medical facilities using GE Healthcare Allia IGS 7 OR x-ray systems are most at risk. Patients undergoing procedures with these systems could be affected if the equipment malfunctions.
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.
Look for serial numbers D3-23-026 or D4-24-002 on the Allia IGS 7 OR x-ray systems.
GE Healthcare has found that adhesive material might not have been applied to some bolts of certain models, which could cause the detector or X-ray tube to fall.
The detector or X-ray tube could fall, potentially causing injury to medical staff or patients during procedures.
Check for serial numbers D3-23-026 or D4-24-002 and UDI/DI code 00195278215550 on the Allia IGS 7 OR x-ray systems.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1781-2024 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-1781-2024 from GE Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
