Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Arietta 70 Ultrasound System Intended for use by trained personnel (doctor Recalled by Hitachi Medical Systems America Inc Due to The strength of the arm mounting mechanism was...

Date: May 2, 2017
Company: Hitachi Medical Systems America Inc
Status: Terminated
Source: FDA (Device)

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 Hitachi Medical Systems America Inc directly.

Affected Products

Arietta 70 Ultrasound System Intended for use by trained personnel (doctor, sonographer. etc.) for the diagnostic Ultrasound evaluation.

Quantity: 77

Why Was This Recalled?

The strength of the arm mounting mechanism was insufficient and had to be redesigned.

Where Was This Sold?

This product was distributed to 18 states: AZ, CA, FL, HI, IL, ME, MD, MA, MN, MO, NJ, NY, NC, OH, PA, SC, TN, TX

Affected (18 states)Not affected

About Hitachi Medical Systems America Inc

Hitachi Medical Systems America Inc has 17 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report