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Floor Lamps Recalled Due To Fire and Shock Hazard

Home Source Industries LLC is recalling brown metal floor lamps with alabaster glass shades. The lamps can short circuit due to defective sockets, posing fire and shock hazards.

Alere, Inc. Recalls INRatio Monitoring Systems

Alere, Inc. is voluntarily recalling their INRatio® and INRatio®2 PT/INR Monitoring System after working with the U.S. Food and Drug Administration (FDA).

FDA Publishes Final Guidance for Medical Device EMC

The U.S. Food and Drug Administration (FDA) issues final guidance for medical device electromagnetic compatibility (EMC). The final guidance document details a number of primary components that are needed from U.S. manufacturers in order to obtain premarket clearance or approval for supporting claims of medical device EMC.

Laboratory Continues U.S. EMC Testing Services Expansion

Element has announced the July 1, 2016 acquisition of Northwest EMC, further expanding their...

EU Commission Releases 2015 RAPEX Summary Statistics on Unsafe Consumer Products

The Commission of the European Union (EU) has released statistics on notices of unsafe...
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FDA Proposes Ban on Electrical Stimulation Devices for Behavioral Conditioning

The U.S. Food and Drug Administration (FDA) has proposed a ban on electrical stimulation...

EU Commission Releases Draft Guidance on New EMC Directive

The Commission of the European Union (EU) has released a draft guidance document on...

FCC Invites Comments on Eliminating Gain Limit on Amateur Amplifiers

The U.S. Federal Communications Commission (FCC) is seeking comments on a proposed change in its regulations...

The New Australian Regulatory Compliance Mark

The RCM is now mandatory for electrical safety in Australia and New Zealand On March...

Towards a Logic-Based Extension of a Relational Software Tool for Coherent Technical Documentation of Medical Devices

This work presents a novel software tool intended to support compilation of coherent technical...
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