Ellerbee v. Ethicon, Inc.

District Court, M.D. Florida·Decided September 2, 2020·No. 8:20-cv-01514·Unknown

Opinion

UNITED STATES DISTRICT COURT MIDDLE DISTRICT OF FLORIDA TAMPA DIVISION

OVIS ELLERBEE and JAMES ELLERBEE,

Plaintiffs,

v. Case No. 8:20-cv-1514-T-60AEP

ETHICON, INC. and JOHNSON & JOHNSON,

Defendants. /

ORDER GRANTING IN PART AND DENYING IN PART “DEFENDANTS’ MOTION FOR SUMMARY JUDGMENT”

This matter is before the Court on “Defendants’ Motion for Summary Judgment” and supporting memorandum, filed on October 29, 2019. (Docs. 37; 38). Plaintiffs responded in opposition on November 15, 2019. (Doc. 47). Defendants filed a reply on November 21, 2019. (Doc. 49). Upon review of the motion, response, reply, court file, and record, the Court finds as follows: Background This case is one of thousands of similar cases filed since 2010.1 Plaintiffs Ovis Ellerbee and James Ellerbee sued directly in the Southern District of West

1 In the seven MDLs, over 100,000 cases have been filed, approximately 40,000 of which are in the Ethicon MDL. See MDL 2187 (C.R. Bard) Member List of Cases, https://www.wvsd.uscourts.gov/caselist/caseviewlist.aspx?mdl=2187; MDL 2325 (American Medical Systems) Member List of Cases, https://www.wvsd.uscourts.gov/caselist/caseviewlist.aspx?mdl=2325; MDL 2326 (Boston Scientific) Member List of Cases, https://www.wvsd.uscourts.gov/caselist/caseviewlist.aspx?mdl=2326; MDL 2327 (Johnson & Johnson, Ethicon) Member List of Cases, https://www.wvsd.uscourts.gov/caselist/caseviewlist.aspx?mdl=2327; Virginia as part of the multidistrict litigation (MDL) entitled In re: Ethicon, Inc., Pelvic Repair Sys. Prods. Liab. Lit., MDL No. 2327. The case was not resolved by the MDL transferee court (“MDL Court”), and on July 1, 2020, it was transferred to

this Court. On November 7, 2006, Ms. Ellerbee was implanted with Ethicon’s TVT-O and Prolift devices at a hospital in Tampa, Florida. Both devices were designed and manufactured by Defendants Johnson & Johnson and Ethicon, Inc. In early 2017, Ms. Ellerbee’s physician surgically removed what Plaintiffs claim to have been mesh located in the bladder mucosa. On February 23, 2017, Ms. Ellerbee

underwent a revision/removal procedure and an anterior colporrhaphy. Ms. Ellerbee later had another mesh sling implanted. On June 24, 2015, Plaintiffs sued directly in the MDL using a short-form complaint, alleging: Negligence (Count I), Strict Liability – Manufacturing Defect (Count II), Strict Liability – Failure to Warn (Count III), Strict Liability – Defective Product (Count IV), Strict Liability – Design Defect (Count V), Common Law Fraud (Count VI), Fraudulent Concealment (Count VII), Constructive Fraud (Count VIII),

Negligent Misrepresentation (Count IX), Negligent Infliction of Emotional Distress (Count X), Breach of Express Warranty (Count XI), Breach of Implied Warranty (Count XII), Violation of Consumer Protection Laws (Count XIII), Gross Negligence

MDL 2387 (Coloplast) Member List of Cases, https://www.wvsd.uscourts.gov/caselist/caseviewlist.aspx?mdl=2387; MDL 2440 (Cook Medical) Member List of Cases, https://www.wvsd.uscourts.gov/caselist/caseviewlist.aspx?mdl=2440; and MDL 2511 (Neomedic) Member List of Cases, https://www.wvsd.uscourts.gov/caselist/caseviewlist.aspx?mdl=2511. (Count XIV), Unjust Enrichment (Count XV), Loss of Consortium (Count XVI), Punitive Damages (Count XVII), and Discovery Rule and Tolling (Count XVIII). Legal Standard

Summary judgment is appropriate “if the movant shows that there is no genuine dispute as to any material fact and the movant is entitled to judgment as a matter of law.” Fed. R. Civ. P. 56(a). A properly supported motion for summary judgment is only defeated by the existence of a genuine issue of material fact. Anderson v. Liberty Lobby, Inc., 477 U.S. 242, 249 (1986). The moving party bears the initial burden of showing that there are no

genuine issues of material fact. Hickson Corp. v. N. Crossarm Co., 357 F.3d 1256, 1260 (11th Cir. 2004). When the moving party has discharged its burden, the nonmoving party must then designate specific facts showing the existence of genuine issues of material fact. Jeffery v. Sarasota White Sox, Inc., 64 F.3d 590, 593-94 (11th Cir. 1995). If there is a conflict between the parties’ allegations or evidence, the nonmoving party’s evidence is presumed to be true and all reasonable inferences must be drawn in the nonmoving party’s favor. Shotz v. City of

Plantation, 344 F.3d 1161, 1164 (11th Cir. 2003). Analysis Statute of Limitations Defendants seek summary judgment on all claims, arguing that the entire action is barred by the statute of limitations.2 Under Florida law, the statute of

2 For reasons explained in the Court’s analysis of Count XIII, this analysis does not apply to that count. limitations for a product’s liability action is four years. §§ 95.11(3)(e), 95.031, F.S. “The limitations period does not begin to run until ‘the date that the facts giving rise to the cause of action were discovered, or should have been discovered with the

exercise of due diligence.’” Eghnayem v. Boston Sci. Corp., 873 F.3d 1304, 1323 (11th Cir. 2017) (quoting § 95.031, F.S.). The knowledge required for the limitations period to begin to run does not need to “rise to that of legal certainty.” Id. (quoting Univ. of Miami v. Bogorff, 583 So. 2d 1000, 1004 (Fla. 1991)). Instead, plaintiffs are only required to have “notice, through the exercise of reasonable diligence, of the possible invasion of their legal rights.” Id. (quoting Bogorff, 583 So.

2d at 1004). Notice has two essential components: a distinct injury and exposure to the product at issue. Id. Therefore, to warrant summary judgment based on the statute of limitations, the evidence must clearly establish that more than four years before Plaintiffs filed suit, they were aware of a distinct change in Ms. Ellerbee’s condition and knew that Ms. Ellerbee was exposed to the products at issue. Here, the record does not establish that Plaintiffs were aware of a distinct change in Ms. Ellerbee’s condition, or that she knew of the possible involvement of

the devices, by June 24, 2011. Although Ms. Ellerbee reported vaginal pain in 2007 and 2009, this symptom was not so obviously unusual as to put Plaintiffs on notice of their possible claims, particularly because Ms. Ellerbee had reported vaginal pain and other similar symptoms prior to the implantation of the devices. See id. at 1324 (explaining that emergence of a new symptom was not so obviously unusual as to put the plaintiff on notice as to her possible claim and holding that the timeliness of the action was therefore a fact question for the jury). Additionally, according to Ms. Ellerbee’s deposition testimony, she was not aware of the possible involvement of the devices until 2013, when she saw a television commercial describing her

symptoms and decided to seek medical care. (Doc. 37-3). Consequently, the record does not conclusively establish that the limitations period expired before Plaintiffs filed their complaint. Consequently, the motion for summary judgment is denied on this ground. Count I: Negligence Manufacturing Defect

Defendants seek summary judgment on Count I to the extent the claim is based on an alleged manufacturing defect.

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