Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2315-2018 — 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.

U.S. FDA — Device Enforcement · United States · 2018-01-04 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2315-2018
Date of alert: 2018-01-04
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Toshiba American Medical Systems Inc
Product category: device
Product type: Devices

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-2315-2018 — 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.

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