AS Software recalls version 7.82: Software changes without testing may cause ultrasound measurements to be inaccurate. Affected users should verify their software version and contact support.
Any change made to current ultrasound machine software or hardware upgrades, adding or modifying custom fields, or adding a new Ultrasound Machine, must be tested prior to the use in production environment to ensure that ultrasound measurements are crossing over correctly to the AS system
AS Software recalls its OB-GYN Information System version 7.824.x because software changes or hardware upgrades without proper testing can lead to incorrect ultrasound measurements. This could affect pregnancy monitoring accuracy if not fixed.
The software requires testing after any changes to ultrasound machine settings to ensure measurements cross over correctly to the system. Without testing, ultrasound data may be inaccurate, potentially affecting pregnancy monitoring.
Healthcare providers using the AS OB-GYN Information System version 7.824.x for ultrasound measurements. Those who have made software changes without testing are most at risk.
Check for software version 7.824.x on the AS OB-GYN Information System. The product was sold through AS Software's channels.
Check your system's software version to confirm it is 7.824.x.
The recall is because changes to the software or hardware without proper testing can cause ultrasound measurements to be inaccurate.
Check for software version 7.824.x on the AS OB-GYN Information System.
Verify your software version and contact AS Software for guidance on testing changes.
We’ve drafted a message you can send AS Software to request your refund or repair — edit it as you like.
Subject: Recall Z-0118-2019 — AS Software AS Software Hello, I own a AS Software that is covered by recall Z-0118-2019 from AS Software. 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.
