Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AS-OBGYN Information System version 7.824.x Recalled by AS Software, Inc. Due to Any change made to current ultrasound machine software...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact AS Software, Inc. directly.
Affected Products
AS-OBGYN Information System version 7.824.x
Quantity: 52 systems
Why Was This Recalled?
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
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About AS Software, Inc.
AS Software, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report