Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Aplio XG Diagnostic Ultrasound System SSA-790A Used for routine diagnostic Recalled by Toshiba American Medical Systems Inc Due to The firm initiated this recall of certain Toshiba...
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 Toshiba American Medical Systems Inc directly.
Affected Products
Aplio XG Diagnostic Ultrasound System SSA-790A Used for routine diagnostic imaging
Quantity: 430 (1352 total)
Why Was This Recalled?
The firm initiated this recall of certain Toshiba Diagnostic Ultrasound Systems because it has been found that under certain conditions, the temperature of the transducer head may increase in 2D+PW mode or 2D+CDI (POWER, ADF) +PW mode. When the system is used under both conditions listed below, the temperature of the transducer head connected to the system may increase in temperature and possibly
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Toshiba American Medical Systems Inc
Toshiba American Medical Systems Inc has 56 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report