Reported Feb 24, 2016 · Terminated

MEE-1000A Neuromaster, Model No. Accessories: MS-110B (Electric Stimulation), MS-120BK (Current Stimulator Box)…

Nihon Kohden America 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: Nihon Kohden America Inc · 15353 Barranca Pkwy · Irvine, CA · 92618-2216

Is this the product you have?

  • MEE-1000A Neuromaster, Model No
  • Accessories
    • MS-110B (Electric Stimulation)
    • MS-120BK (Current Stimulator Box) JB-116B
    • JB-132B (Amplifiers) Electromyography. (EMG)
Lot codes and dates
  • Serial Numbers
    • MS-110B: (17 units) 00013-00019
    • 00023- 00032
  • MS-120BK(6
  • units) 0009- 00014 JB-116B
    • (31 units)
    • 0008
    • 00012
    • 00014
    • 00016
    • 00018
    • 00019
    • 00020
    • 00021
    • 00023
    • 00025
    • 00026
    • 00027
    • 00028
    • 00029
    • 00031
    • 00032
    • 00034
    • 00035
    • 00039
    • 00043
    • 00102
    • 00103
    • 00122-00128
    • 00134
    • 00135
  • JB-132B
    • (83 units) 00009
    • 00011
    • 00012
    • 00014
    • 00015
    • 00016
    • 00018
    • 00019
    • 00020
    • 00021
    • 00023
    • 00024
    • 00025
    • 00026
    • 00027
    • 00036
    • 00037
    • 00038
    • 00041
    • 00042
    • 00043
    • 00044
    • 00046
    • 00047
    • 00049
    • 00061
    • 00062
    • 00066
    • 00067
    • 00068
    • 00069
    • 00071
    • 00072
    • 00074
    • 00075
    • 00082
    • 00084
    • 0085
    • 00086
    • 00090
    • 00095
    • 00099
    • 00120
    • 00121-00129
    • 00131-00147
    • 00149-00155
    • 00157
    • 00161
    • 00164-00168
Amount recalled
477 units total (137 units in US)

Where it was sold

  • Nationwide

Why it was recalled

The MEE-1000A Neuromaster had defective printed circuit boards (PCBs). Gas arrestors on these boards which were intended to provide protection from electrostatic discharge failed to prohibit unintentional current flow.

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 Nihon Kohden America 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 Feb 22, 2016 · Data as of Sep 19, 5:20 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.