# FDA recall Z-2315-2018

> **Toshiba American Medical Systems Inc** · Class II · device recall initiated 2018-01-04.

## Product

Diagnostic Ultrasound System, Aplio I-series.  Labeled as i700, i800, i900    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.

## Reason for recall

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.

## Distribution

USA (nationwide) Distribution to the states of : CA, CO, DE, GA, HI, IA, ID, IL, IN, MD, MI, MN, MO, NC, ND, NV, OH, OR, PA, SC, SD, TN, TX, VA, WA, WV and WY.

## Key facts

- **Recall number:** Z-2315-2018
- **Recalling firm:** Toshiba American Medical Systems Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-01-04
- **Report date:** 2018-07-04
- **Termination date:** 2023-10-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tustin, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2315-2018

## Citation

> AI Analytics. FDA recall Z-2315-2018. Retrieved 2026-06-04 from https://api.ai-analytics.org/recall/Z-2315-2018. Source: US FDA. Licensed CC0.

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