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Valuable Piece on Class Action Fairness Act (“CAFA”) Advanced Removal Strategies – Distributed with Permission

By Bexis on May 17, 2022
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We’re not the font of all legal knowledge; we don’t claim to be.  Every now and then we come across material published by our colleagues at other firms defending prescription medical product liability litigation that we think would be valuable to our readers, so we ask if we can republish.  That’s how our 50-state survey on state tolling statutes came about.  It was a piece by another firm that we thought would be useful to our readers dealing with unsuccessful would-be forum shoppers, so we inquired, and they were gracious enough to allow us to distribute their research to our readers.

Recently, we were duly impressed by a Greenberg Traurig class action-related “advisory” entitled “Class Action Fairness Act Advanced Removal Strategies.”  It was written by Greenberg partners, Ryan C. Bykerk, and Christopher S. Dodrill.  This advisory is richly enough researched that it looks and reads like a law review article – which we at the Blog appreciate.  Here’s a thumbnail list of the CAFA topics covered:

  • Timing of CAFA removal, including defense ability to remove on their “own information” at any time.
  • How courts respond to plaintiffs gaming CAFA’s 100-member “mass tort” threshold.
  • Sufficiency of removal allegations concerning CAFA minimal diversity.
  • Citizenship of various types of entities involved in CAFA litigation.
  • Determining and pleading CAFA’s $5 million amount-in-controversy requirement.
  • Post-removal attempts by plaintiffs to destroy CAFA jurisdiction.
  • Defense-side jurisdictional discovery in CAFA cases.
  • Viability of successive CAFA removals.

We’ve uploaded a copy of this piece here, or if you’re so inclined, you can read it on Greenberg Traurig’s website, here.

On multiple occasions the Blog has addressed CAFA-related topics, occasionally with research posts but more frequently discussing new significant decisions.  We’re pleased to add this piece to the resources available to our readers.

Photo of Bexis Bexis

JAMES M. BECK is Reed Smith’s only Senior Life Sciences Policy Analyst, resident in the firm’s Philadelphia office. He is the author of, among other things, Drug and Medical Device Product Liability Handbook (2004) (with Anthony Vale). He wrote the seminal law review…

JAMES M. BECK is Reed Smith’s only Senior Life Sciences Policy Analyst, resident in the firm’s Philadelphia office. He is the author of, among other things, Drug and Medical Device Product Liability Handbook (2004) (with Anthony Vale). He wrote the seminal law review article on off-label use cited by the Supreme Court in Buckman v. Plaintiffs Legal Committee. He has written more amicus briefs for the Product Liability Advisory Council than anyone else in the history of the organization, and in 2011 won PLAC’s highest honor, the John P. Raleigh award. He has been a member of the American Law Institute (ALI) since 2005. He is the long-time editor of the newsletter of the ABA’s Mass Torts Committee.  He is vice chair of the Class Actions and Multi-Plaintiff Litigation SLG of DRI’s Drug and Device Committee.  He can be reached at jmbeck@reedsmith.com.  His LinkedIn page is here.

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  • Posted in:
    Food, Drug & Agriculture
  • Blog:
    Drug & Device Law
  • Organization:
    Reed Smith LLP
  • Article: View Original Source

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