Reported Apr 4, 2018 · Terminated

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

Konica Minolta Medical Imaging USA, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Konica Minolta Medical Imaging USA, Inc. · 411 Newark Pompton Tpke · Wayne, NJ · 07470-6657

Is this the product you have?

  • Sonimage HS1 Ultrasound Kit AC adapter
  • Product NumberA8AR
  • UDI04560141941588
Lot codes and dates
  • Serial Numbers (each has "A8AR-"
  • prefix)
    • 00068
    • 00031
    • 00062
    • 00066
    • 00063
    • 00047
    • 00065
    • 00032
    • 00064
    • 00028
    • 00069
    • 00060
    • 00027
    • 00067
    • 00061
    • 00001
    • 00002
Amount recalled
17

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

Why it was 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.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Konica Minolta Medical Imaging USA, Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Oct 28, 2019 · Data as of Sep 19, 5:33 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.