Sims v. Medtronic Inc et al
Debra Sims |
Medtronic, Inc., Medtronic Inc, Medtronic Logistics LLC, Medtronic Puerto Rico Operations Co and Medtronic USA Inc |
3:2020cv02872 |
September 16, 2020 |
US District Court for the Northern District of Texas |
Brantley Starr |
Torts/Pers Inj: Health Care/Pharmaceutical Pers Inj/Product Liability |
28 U.S.C. ยง 1332 |
Plaintiff |
Docket Report
This docket was last retrieved on June 4, 2021. A more recent docket listing may be available from PACER.
Document Text |
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Filing 5 Summons Issued as to Medtronic Inc, Medtronic Logistics LLC, Medtronic Puerto Rico Operations Co, Medtronic USA Inc. (ykp) |
Filing 4 Request for Clerk to issue Summons filed by Debra Sims. (Presby, Ellen) |
Filing 3 New Case Notes: A filing fee has been paid. Pursuant to Misc. Order 6, Plaintiff is provided the Notice of Right to Consent to Proceed Before A U.S. Magistrate Judge (Judge Ramirez). Clerk to provide copy to plaintiff if not received electronically. (mjr) |
Filing 2 ADDITIONAL ATTACHMENTS to #1 Complaint. (Presby, Ellen) Modified text on 9/17/2020 (mjr). |
Filing 1 COMPLAINT WITH JURY DEMAND against Debra Sims filed by Debra Sims. (Filing fee $400; Receipt number 0539-11178980) Summons(es) not requested at this time. In each Notice of Electronic Filing, the judge assignment is indicated, and a link to the # Judges Copy Requirements and # Judge Specific Requirements is provided. The court reminds the filer that any required copy of this and future documents must be delivered to the judge, in the manner prescribed, within three business days of filing. Unless exempted, attorneys who are not admitted to practice in the Northern District of Texas must seek admission promptly. Forms, instructions, and exemption information may be found at www.txnd.uscourts.gov, or by clicking here: # Attorney Information - Bar Membership. If admission requirements are not satisfied within 21 days, the clerk will notify the presiding judge. (Attachments: #1 Exhibit(s) FDA Warning Letter 2006, #2 Exhibit(s) FDA Warning Letter 2007, #3 Exhibit(s) FDA Form 483 2007, #4 Exhibit(s) FDA Warning Letter 2009, #5 Exhibit(s) FDA Form 483 2008, #6 Exhibit(s) FDA Warning Letter 2012, #7 Exhibit(s) FDA Form 483 2013, #8 Exhibit(s) FDA Recall No. Z-0896-2018, #9 Exhibit(s) Letter from Mike Ronningen, #10 Exhibit(s) FDA Recall No. Z-1570-2014, #11 Exhibit(s) Letter from Mike Crader, #12 Exhibit(s) FDA Recall No. Z-2382-2008, #13 Exhibit(s) Letter from George Aram, #14 Exhibit(s) FDA Recall No. Z-1573-2013, #15 Exhibit(s) Complaint for Permanent Injunction, #16 Exhibit(s) Consent Decree of Permanent Injunction, #17 Exhibit(s) Intentionally Left Blank, #18 Exhibit(s) Medtronic Urgent Medical Device Correction, #19 Exhibit(s) FDA Recall No. Z-1150-2008) (Presby, Ellen) |
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