Class II — Potential Health Hazard

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

Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical Imaging USA, Inc. Due to There is a risk of circuit board breakage...

Date: December 4, 2017
Company: Konica Minolta Medical Imaging USA, 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 Konica Minolta Medical Imaging USA, Inc. directly.

Affected Products

Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A8AR, UDI: 04560141941588

Quantity: 17

Why Was This Recalled?

There is a risk of circuit board breakage within the main housing of the AC Adapter unit. Smoke may be emitted from the AC Adapter as a direct result.

Where Was This Sold?

This product was distributed to 34 states: AL, AZ, CA, CO, CT, FL, GA, HI, IL, IN, IA, KY, LA, MD, MA, MI, MN, MS, MO, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, WA, WI

Affected (34 states)Not affected

About Konica Minolta Medical Imaging USA, Inc.

Konica Minolta Medical Imaging USA, Inc. has 6 total recalls tracked by RecallDetector.

Related Recalls

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