Medtronic, Inc. v. Stengel
Certiorari Denied
Petition for certiorari denied on June 23, 2014.
Issue
Whether the Medical Device Amendments to the federal Food, Drug, and Cosmetic Act preempt a state-law claim alleging that a medical device manufacturer violated a duty under federal law to report adverse-event information to the Food and Drug Administration. CVSG: 10/07/2013.
Mar 28, 2013Application (12A931) to extend the time to file a petition for a writ of certiorari from April 10, 2013 to June 9, 2013, submitted to Justice Kennedy.
Apr 1, 2013Application (12A931) granted by Justice Kennedy extending the time to file until May 10, 2013.
May 10, 2013Petition for a writ of certiorari filed. (Response due June 13, 2013)May 30, 2013Order extending time to file response to petition to and including July 15, 2013.
Jun 10, 2013Brief amicus curiae of DRI -The Voice of the Defense Bar filed.Jun 13, 2013Brief amici curiae of Washington Legal Foundation, et al filed.Jun 13, 2013Brief amicus curiae of Product Liability Advisory Council, Inc. filed.Jul 15, 2013Brief of respondents Richard Stengel, and Mary Lou Stengel in opposition filed.Jul 30, 2013Reply of petitioner Medtronic, Inc. filed.Jul 31, 2013DISTRIBUTED for Conference of September 30, 2013.
Oct 7, 2013The Solicitor General is invited to file a brief in this case expressing the views of the United States.May 20, 2014Brief amicus curiae of United States filed.
May 30, 2014Suggestion of death of respondent Richard Stengel filed by respondent Mary Lou Stengel.
Jun 3, 2014DISTRIBUTED for Conference of June 19, 2014.
Jun 3, 2014Response from petitioner Medtronic, Inc. to respondent's suggestion of death filed. (Distributed)Jun 3, 2014Supplemental brief of petitioner Medtronic, Inc. filed. (Distributed)Jun 23, 2014Petition DENIED.
Recommended Citation: Medtronic, Inc. v. Stengel, SCOTUSblog, https://www.scotusblog.com/cases/medtronic-inc-v-stengel/