Reported Apr 4, 2018 · Terminated

Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A7AP, UDI: 04560141940031

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 NumberA7AP
  • UDI04560141940031
Lot codes and dates
  • Serial Numbers (each has "A7AP-"
  • prefix)

    88 of 88 codes

    • 00045
    • 00041
    • 00004
    • 00076
    • 00090
    • 00016
    • 00037
    • 00038
    • 00060
    • 00059
    • 00091
    • 00028
    • 00089
    • 00080
    • 00077
    • 00039
    • 00057
    • 00040
    • 00007
    • 00043
    • 00024
    • 00071
    • 00003
    • 00064
    • 00011
    • 00052
    • 00027
    • 00006
    • 00044
    • 00042
    • 00063
    • 00078
    • 00087
    • 00047
    • 00031
    • 00048
    • 00008
    • 00068
    • 00095
    • 00103
    • 00096
    • 00098
    • 00097
    • 00099
    • 00100
    • 00101
    • 00102
    • 00082
    • 00084
    • 00092
    • 00083
    • 00069
    • 00079
    • 00061
    • 00019
    • 00072
    • 00081
    • 00051
    • 00018
    • 00017
Amount recalled
88

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.

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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, 4:53 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.