GE Healthcare 1006-9320-000 - Product Catalog
Certain Aespire and Aestiva Anesthesia Systems were noted to have a vulnerability to a cyber-attack when connected to the hospital network. An insufficiently secured terminal server may provide an opportunity for a malicious actor that has already penetrated the hospital network to send fraudulent flow sensor correction parameters.
GE Healthcare 1006-9320-000 is a product code used in their catalog. This code represents a specific product or component within GE Healthcare's product line. The product code 1006-9320-000 is associated with various components such as AMVF, AMVG, AMVE, AMVH, and AMVJ series products.
This is a standard product code from GE Healthcare and does not indicate any security risk or malicious activity. The code is used for internal tracking and product identification within GE Healthcare's systems.
GE Healthcare customers
Check for any unusual patterns or behaviors associated with the product code in your system. Since this is a standard product code, it is not inherently dangerous.
Verify that the product code 1006-9320-000 is part of a legitimate GE Healthcare product catalog.
Ensure that any system using this product code is properly configured and maintained to prevent unauthorized access or misuse.
The product code 1006-9320-000 is a standard code used by GE Healthcare for internal tracking and product identification. It does not indicate any security risk.
No, this product code is not dangerous. It is a standard code used in GE Healthcare's product catalog and does not pose any security risks.
Ensure that your system is properly configured and maintained to prevent unauthorized access or misuse of the product code.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0116-2020 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-0116-2020 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.
