MEE-1000A Neuromaster, Model No. Accessories: MS-110B (Electric Stimulation), MS-120BK (Current Stimulator Box) JB-116B, JB-132B (Amplifiers) Electromyography. (EMG)
Reported: February 24, 2016 Initiated: January 19, 2012 #Z-0817-2016
Product Description
MEE-1000A Neuromaster, Model No. Accessories: MS-110B (Electric Stimulation), MS-120BK (Current Stimulator Box) JB-116B, JB-132B (Amplifiers) Electromyography. (EMG)
Reason for Recall
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.
Details
- Recalling Firm
- Nihon Kohden America Inc
- Units Affected
- 477 units total (137 units in US)
- Distribution
- Worldwide distribution. US nationwide, Australia, Austria, France, Germany, Greece, Japan, Romania, South Africa, South Korea, Spain, and United Kingdom.
- Location
- Irvine, CA
Frequently Asked Questions
What product was recalled? ▼
MEE-1000A Neuromaster, Model No. Accessories: MS-110B (Electric Stimulation), MS-120BK (Current Stimulator Box) JB-116B, JB-132B (Amplifiers) Electromyography. (EMG). Recalled by Nihon Kohden America Inc. Units affected: 477 units total (137 units in US).
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 24, 2016. Severity: Moderate. Recall number: Z-0817-2016.
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