HOME ABOUT US PRACTICE AREAS CURRENT CASES ATTORNEYS EXPERIENCE & RESULTS NEWSROOM CONTACT US

KHORRAMI LLP May 2011 Newsletter
KHORRAMI LLP Monthly Update

In This Issue

Ninth Circuit Decision Finding Digital Music Downloads Constitute a “License” Rather than a “Sale” Gives Rise to Potentially Massive Class Action Lawsuit for Unpaid Royalties
Labels Matter
Medical Device Approval and the Future of the 510 (k) Process
 
Ninth Circuit Decision Finding Digital Music Downloads Constitute a “License” Rather than a “Sale” Gives Rise to Potentially Massive Class Action Lawsuit for Unpaid Royalties
by KATIE MCSWEENEY, ESQ.

In 2007, F.B.T. Productions, the label that first signed rap artist Eminem to a recording contract, filed suit for breach of contract against Universal Music Group subsidiary Aftermath Records, with which F.B.T. contracted for exclusive rights to Eminem’s recordings. Under the contract, Aftermath was required to pay the artist 12%-20% of the adjusted retail price for every record sold, and 50% for every record “licensed”. The gravamen of F.B.T.’s complaint was that UMG had breached this agreement as to digital downloads by paying royalties at the lesser rate designated for a record “sale” rather than the significantly higher rate for a record “license”, based on its position that digital downloads are more akin to a the licensing of a record than the physical sale of a record.
[Read More]

Labels Matter
By ELIZABETH HALL, ESQ.

“Simply stated: labels matter.” These were the words of the California Supreme Court in its recent decision, Kwikset Corporation v. Orange County, 51 Cal.4th 310, 328 (2011), when it determined that consumers will chose one product over another because of a label, amongst other things. In fact, the Court noted how an entire body of trademark law has been created to “protect commercial and consumer interests in accurate label representations as to source, because consumers rely on the accuracy of those representations in making their buying decisions.” Id.
[Read More]

Medical Device Approval and the Future of the 510 (k) Process
By BAHAR DEJBAN, ESQ.

Currently, there are two major processes by which medical devices requiring U.S. Food and Drug Administration (FDA) review come to the American market. Medical devices receive approval either Pre-Market Approval (PMA) or receive clearance to market through the 510(k) process.
[Read More]

This newsletter is not intended to provide legal advice on specific subjects, but rather to share insights and invite discussion about news and issues in consumer law. If you have specific legal questions or would like to discuss a potential case, we invite you to contact us via e-mail or by phone, 213.596.6000.