Toshiba recalls Aplio i700, i800, i900 ultrasound systems where the power supply may fail to start when plugged in with the main switch set to ON. Affected units have specific model and serial numbers.
The power supply unit may be damaged and may fail to start up when the power plug is inserted into a power outlet while the main power switch on the rear of the system is set to ON.
Toshiba is recalling Aplio I-series ultrasound systems (i700, i800, i900) because the power supply unit might fail to start when plugged in while the main switch is set to ON. This could cause the system to not power on properly, potentially leading to operational issues.
The power supply unit may become damaged and fail to start when the power plug is inserted into an outlet while the main power switch on the system's rear is set to ON. This could prevent the ultrasound system from operating correctly.
Medical professionals using the Aplio I-series ultrasound systems are most at risk. Affected units have specific model numbers (TUS-AI700, TUS-AI800, TUS-AI900) and serial numbers listed in the recall.
Check for model numbers TUS-AI700, TUS-AI800, or TUS-AI900 on the device. Affected units have specific serial numbers listed in the recall notice.
Ensure the main power switch on the rear of the system is set to OFF before plugging in the power cord.
The power supply unit may be damaged and fail to start when plugged in with the main switch set to ON.
The Aplio i700, i800, and i900 models (model numbers TUS-AI700, TUS-AI800, TUS-AI900).
Check the model number on your device and compare it to TUS-AI700, TUS-AI800, or TUS-AI900. Affected units also have specific serial numbers listed in the recall.
We’ve drafted a message you can send Toshiba to request your refund or repair — edit it as you like.
Subject: Recall Z-2315-2018 — Toshiba Toshiba Hello, I own a Toshiba that is covered by recall Z-2315-2018 from Toshiba. 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.
