Blouin v. Surgical Sense

CourtSuperior Court of Rhode Island
DecidedMay 12, 2008
DocketC.A. No. PC 07-6855
StatusPublished

This text of Blouin v. Surgical Sense (Blouin v. Surgical Sense) is published on Counsel Stack Legal Research, covering Superior Court of Rhode Island primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Blouin v. Surgical Sense, (R.I. Ct. App. 2008).

Opinion

DECISION
Davol Inc. and C.R. Bard Inc. ("Defendants") move to dismiss the complaint of William Blouin ("Mr. Blouin") and Donna Blouin (collectively "Plaintiffs") pursuant to R.I. Super. Civ. P. 12(b)(6). Plaintiffs object to the motion.

I
Facts and Travel
On December 19, 2007, Plaintiffs filed a complaint in this Court, alleging that Mr. Blouin had been severely injured by the defective and dangerous condition of a Kugel Mesh Patch ("Kugel Patch") designed, manufactured, and distributed by Defendants. Mr. Blouin had a hernia repair on November 18, 1999. A Kugel Patch, then a product of Surgical Sense, Inc. ("Surgical Sense") was implanted. The Kugel Patch used in that operation was comprised of a segment of mesh held in a round or oval shape by a "memory recoil ring." The "memory recoil ring" is a plastic coil ring designed to aid in the deployment of the polypropylene mesh hernia patch. Defendants acquired the Kugel Patch product line from Surgical Sense in January 2000. In 2004, Mr. Blouin suffered severe chronic abdominal pain for which he was hospitalized. Mr. *Page 2 Blouin underwent exploratory abdominal surgery on April 1, 2004. During that surgery, the operating physician discovered that the mesh of the Kugel Patch had folded on itself and presented as a mass in the peritoneal space. The folded mesh pushed against the abdominal walls and structures, and closed an area within the peritoneum that is usually open in a healthy abdomen. The operating surgeon explanted the Kugel Patch. Mr. Blouin endured a lengthy and painful recovery period.

Plaintiffs contend that Mr. Blouin's injuries were the result of a dangerous defect in Defendants' product. Plaintiffs further contend that Defendants conducted post market design research in 2002, which resulted in unfavorable comments and complaints from physicians using the product. Plaintiffs allege that Defendants either fraudulently concealed these results or negligently failed to monitor them. Plaintiffs claim that Defendants uncovered a serious design defect in the memory recoil ring of the Kugel Patch no later than September 2004, and withheld knowledge of this defect until 2005. In 2005, Defendants initiated a partial distribution hold, recalled several specific designs of the Kugel Patch,1 and notified the FDA and the public of the severity of potential complications with its products. Defendants continued to recall various sizes and designs of their products in 2006 and 2007. The product used to repair Mr. Blouin's hernia was not one of the specific products recalled. Plaintiffs contend, however, that Mr. Blouin suffered symptoms and conditions that were very similar to those listed in the Defendants' recall notices.2 Plaintiffs' complaint alleges negligence, strict product liability, *Page 3 negligent infliction of emotional distress, intentional infliction of emotional distress, breach of implied warranty, failure to warn, and fraud.

Defendants have filed the instant motion to dismiss, contending that Plaintiffs' action is untimely under G.L. 1956 § 9-1-14(b). Defendants aver that Plaintiffs knew or should have known of Mr. Blouin's injuries at the time of his explant surgery in April 2004, when his physician noted that the ring had folded on itself. Defendants contend that the three-year time limit imposed by the statute of limitations began to run on April 1, 2004, and that Plaintiffs' claim is time barred, as they did not commence this action until December 2007.

In addition to their statute of limitations argument, Defendants further contend that Plaintiffs will be unable to prove proximate causation. Defendants assert that Mr. Blouin's Kugel Patch was implanted in 1999 — a year before Defendants acquired the Kugel Patch product line from Surgical Sense. Arguing that they never assumed product liability for the assets attained from Surgical Sense, Defendants aver that they cannot be held liable for injury caused by a product that they could not have manufactured, designed, or distributed in 1999.

Plaintiffs oppose the motion to dismiss on the grounds that they were not aware either that the Kugel Patch was dangerously defective, or that the defect caused Mr. Blouin's injury until after Defendants had informed the FDA and the public of the defective condition in 2005. Plaintiffs argue that it was impossible to connect Mr. Blouin's injury to the product's design defect before the Defendants' initial recall in 2005. They contend that the three-year statute of limitations was, therefore, tolled at least until this point. Plaintiffs assert that a 2006 FDA report noted that ring breaks were only one of several possible defects with the Kugel Patch, and because Mr. Blouin's ring folded but did not break, Plaintiffs could not know that his injury was the result of a Kugel Patch defect until after this 2006 report. Plaintiffs additionally contend that *Page 4 their allegations of fraud against Defendants tolls the statute of limitation under G.L. 1956 § 9-1-20. They argue that they have presented factual allegations that Defendants concealed the existence of the defect — and therefore Plaintiffs' cause of action — until either 2005 or 2006, and, therefore, Plaintiffs' 2007 complaint was timely.

Plaintiffs further oppose Defendants' argument regarding proximate cause. Plaintiffs acknowledge the general rule protecting a company from liability when it purchases the assets of another company. However, Plaintiffs argue that Defendants' purchase of the Kugel Patch line of products from Surgical Sense falls within either the "mere continuation" or "de facto merger" exceptions to the general successor-in-interest rule, resulting in Defendants' liability for the Kugel Patch defect.

II
Standard of Review
"When ruling on a Rule 12(b)(6) motion, the trial justice must look no further than the complaint, assume that all allegations in the complaint are true, and resolve any doubts in a [non-movant's] favor." Toste FarmCorp. v. Hadbury, Inc., 798 A.2d 901, 905 (R.I. 2002) (citations omitted). The standard is lenient to the plaintiff, and "[n]o complaint will be deemed insufficient unless it is clear beyond a reasonable doubt that the complainant will be unable to establish his [or her] right to relief under any set of facts which might be proved in support of his [or her] claim." Brough v. Foley, 572 A.2d 63, 68 (R.I. 1990) (citingBragg v. Warwick Shoppers World, 102 R.I. 8, 12, 227 A.2d 582, 584 (R.I. 1967)). It is well-settled that a complaint is not insufficient unless the face of the complaint reveals "some insuperable bar to relief."Hulslander v. Murphy, 633 A.2d 263 (R.I. 1993); Goldstein v. RhodeIsland Hosp. Trust Nat'l Bank, 110 R.I. 580, 586,

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Bluebook (online)
Blouin v. Surgical Sense, Counsel Stack Legal Research, https://law.counselstack.com/opinion/blouin-v-surgical-sense-risuperct-2008.